Implementation and Evaluation of Primary Care Behavioral Health in Sweden (KAIROS)
Primary Purpose
Psychological Distress, Life Style Induced Illness, Life Stress
Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Brief Interventions (BI)
Care As Usual (CAU)
Sponsored by
About this trial
This is an interventional treatment trial for Psychological Distress
Eligibility Criteria
Inclusion Criteria:
- All patients from age 18 who seek care at the PCC, who are deemed to be suitable for Behavioural Health interventions and booked to the mental health professionals at the PCC, according to screening methods and/or clinical assessments made by health care personnel at the PCC, will be included. This broad criteria reflects the naturalistic setting where decisions of clinicians, rather than highly standardized criteria, are the basis for inclusion.
Exclusion Criteria:
- Does not speak Swedish well enough to fill out questionnaires.
- Is in need of emergency type care, like with suicidal ideation or behaviours, ongoing psychosis or mania.
Sites / Locations
- Närhälsan Hjällbo VårdcentralRecruiting
- Närhälsan Bollebygd VårdcentralRecruiting
- Närhälsan Dalsjöfors VårdcentralRecruiting
- Närhälsan Mösseberg VårdcentralRecruiting
- Närhälsan Oden VårdcentralRecruiting
- Närhälsan Gråbo VårdcentralRecruiting
- Närhälsan Eriksberg VårdcentralRecruiting
- Närhälsan Gibraltargatan VårdcentralRecruiting
- Närhälsan Majorna VårdcentralRecruiting
- Närhälsan Sannegården VårdcentralRecruiting
- Närhälsan Solgärde VårdcentralRecruiting
- Närhälsan Tjörn VårdcentralRecruiting
- Närhälsan Ågårdsskogen VårdcentralRecruiting
- Närhälsan Mellerud VårdcentralRecruiting
- Närhälsan Munkedal VårdcentralRecruiting
- Närhälsan Stenungsund VårdcentralRecruiting
- Närhälsan Källstorp VårdcentralRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Implementing PCBH directly
Delayed implementation of PCBH
Arm Description
PCCs randomized to this arm will immediately start the implementation of PCBH.
PCCs randomized to this arm will have a delayed start of their PCBH implementation, waiting between 5-9 months. During this time, the same patient-level and organizational-level data will be collected from these centers while they continue to use traditional primary care / Care As Usual (CAU) .
Outcomes
Primary Outcome Measures
WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (4 domains)
The eight items constituting the four domains of Life activities, Cognition, Getting along, and Participation in the 12-item version of the WHO Disability Assessment Schedule 2.0 (WHODAS-12) will be used as primary outcome, since these are condition-independent measures of Behavioral Health relevant everyday functioning. The scale ranges from 0 to 32 points. A lower score means better functioning. As such, a lower score is a better outcome.
Waiting time until first appointment
Waiting time from the patient contacting their PCC with a behavioural health concern to being seen by a physician or psychosocial resource among patients in the study
Secondary Outcome Measures
WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (2 domains)
The two domains of Mobility and Self-care will be measured and the whole WHODAS will be used in some secondary analyses, but not for the primary outcome since these domains tend to form two independent factors, many patients will have initial adequate function in these domains and they are not expected to change much. The scale ranges from 0 to 48 points. A lower score means better functioning. As such, a lower score is a better outcome.
Third next available appointment (TNAA)
Waiting time until next available appointment for a third hypothetical patient that calls in on a given day for every clinician at the PCC, measured on the same time every week (e. g. Mondays at 9 AM), a measure of access to and and availability of care that is independent of patients own ability to show up at an offered time.
Patient Health Questionnaire 9-Item (PHQ-9)
The full version of a well-validated scale for measuring depressive symptoms. PHQ-9 total score for the nine items ranges from 0 to 27. A lower score means less depressive symptoms. As such, a lower score is a better outcome.
Patient Health Questionnaire 2-Item (PHQ-2)
PHQ-2 consists of two questions from the PHQ-9. This will be administered as part of the PHQ-9 on the above mentioned time points, and will replace the PHQ-9 on the mid-treatment measurements. The scale ranges from 0 to 6 points. A lower score means less depressive symptoms. As such, a lower score is a better outcome.
Generalized Anxiety Disorder 7-item (GAD-7)
The full version of a well-validated scale for measuring anxiety symptoms. GAD-7 total score for the seven items ranges from 0 to 21. A lower score means less anxiety symptoms. As such, a lower score is a better outcome.
Generalized Anxiety Disorder 2-item (GAD-2)
GAD-2 consists of two questions from the GAD-7. This will be administered as part of the GAD-7 on the above mentioned time points, and will replace the GAD-7 on the mid-treatment measurements. The scale ranges from 0 to 6 points. A lower score means less anxiety symptoms. As such, a lower score is a better outcome.
Social Phobia Inventory - Abbreviated version (Mini-SPIN)
Social anxiety symptoms are measured with a very short version of a well established patient-rated scale for social phobia. The scale ranges from 0 to 12 points. A lower score means less symptoms of social anxiety. As such, a lower score is a better outcome.
The Alcohol Use Disorders Identification Test-Concise (AUDIT-C)
Symptoms of alcohol misuse are measured with a very short version of a well established patient-rated scale for alcohol misuse. The scale ranges from 0 to 12 points. A lower score means less symptoms of alcohol misuse. As such, a lower score is a better outcome.
Panic Disorder Severity Scale - Self rated 2-item (PDSS-SR-MINI-2)
Symptoms of panic attacks are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. The scale ranges from 0 to 8 points. A lower score means less symptoms of panic disorder. As such, a lower score is a better outcome.
Karolinska Exhaustion Disorder Scale 3-item (KEDS-3) + 2 confirming questions from the Swedish questionnaire 'självskattat utmattningssyndrom' (s-UMS) ['self-rated burnout-syndrome']
Symptoms of stress-related exhaustion are measured with a very short version of a well established patient-rated scale and has been created by an expert group, who chose three representative questions from the original KEDS scale. To aid with diagnostics, two confirmatory questions from the Swedish s-UMS scale were added, asking for duration and presumed cause of symptoms. The scale ranges from 0 to 18 points. A lower score means less symptoms of stress-related exhaustion. As such, a lower score is a better outcome.
Perceived Stress Scale (PSS-MINI-2) + 2 new questions
Stress symptoms are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. To increase face validity of the very short scale, we also added two more direct questions ("Have you been feeling stressed lately?", "Have you been feeling tense lately?"). The scale ranges from 0 to 16 points. A lower score means less stress symptoms. As such, a lower score is a better outcome.
Insomnia Severity Index 2-item (ISI-MINI-2)
Symptoms of sleep disorders are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. The scale ranges from 0 to 8 points. A lower score means less sleep problems. As such, a lower score is a better outcome.
Short Health Anxiety Inventory 3-item (SHAI-MINI-3)
Symptoms of health anxiety are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. The scale ranges from 0 to 9 points. A lower score means less symptoms of health anxiety. As such, a lower score is a better outcome.
Obsessive Compulsive Disorder 3-Item (OCD-3-MINI)
Symptoms of obsessive compulsive disorder are measured by a very short patient-rated scale and has been created by an expert group. The scale ranges from 0 to 12 points. A lower score means less obsessive/compulsive thoughts and behaviors. As such, a lower score is a better outcome.
Pain One-item Rating
Pain is measured on a scale from 0 to 10, where 0 is no pain and 10 is worst pain imaginable. As such, a lower score is a better outcome.
Total symptom index
Also, a total index for level of symptoms will be calculated from all symptom items, where different weights will be used to balance the different number of questions for different domains, for example to avoid the larger number of items related to anxiety to overshadow depression ratings. The scale ranges from 0 to 20 points. A lower score means less mental health symptoms overall. As such, a lower score is a better outcome.
Brunnsviken Brief Quality of Life Questionnaire (BBQ)
Quality of life will be measure be the 12-item Brunnsviken Brief Quality of life (BBQ-12), asking about importance and fulfilment of six areas (e.g. spare time quality, creative work, and friendship). The scale ranges from 0 to 96 points. A lower score means lower quality of life. As such, a higher score is a better outcome.
Outcome Rating Scale (ORS)
The ORS is a four-item measure designed to assess areas of life functioning known to change as a result of therapeutic intervention. These include symptom distress, interpersonal well-being, social role, and overall well-being, measured by four visual analogue scales. The scale ranges from 0 to 40 points. A lower score means lower satisfaction with life areas. As such, a higher score is a better outcome.
Session Rating Scale (SRS)
The Session Rating Scale (SRS) is a four-item visual analogue scale designed to assess key dimensions of effective therapeutic relationships. These include respect and understanding, relevance of the goals and topics, client-practitioner fit and overall alliance. The scale ranges from 0 to 40 points. A lower score means lower ratings of the therapeutic alliance. As such, a higher score is a better outcome.
Patient-rated perception and attitude toward care provider
9-items previously used in PCBH-settings (self-report), and four items from the Client Satisfaction Questionnaire (CSQ). The scale ranges from 0 to 57 points. A lower score means less satisfaction with care. As such, a higher score is a better outcome.
Description of Behavioral Health Plan (PCBH) as structured note by clinician in medical record
Interview form.
Patient recollection of plan/goal/methods, descriptions of behaviour changes made
Interview form.
Experienced negative/Adverse Events, where the worst and most probably care-induced event is more thoroughly described and rated on severity and perceived cause
Interview form.
Adverse Events-9
9 items asking patients to detail any adverse events that occurred as a result of treatment.
Adverse Events-3
3 items asking patients to detail any adverse events that occurred as a result of treatment.
Well-being Behaviors
11 items asking patients how often (number of days each week) they engage in behaviors related to maintaining physical and mental well-being, such as physical exercise and having adequate sleep hygiene. The first 10 items are summarized as an average where 0 is minimum and 7 is maximum. Higher scores indicate more well-being behaviors and better outcome.
Long-term WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (4 domains)
The same as Primary Outcome, but with a long-term time-frame. The scale ranges from 0 to 32 points. A lower score means better functioning. As such, a lower score is a better outcome.
Full Information
NCT ID
NCT05335382
First Posted
March 13, 2022
Last Updated
April 12, 2022
Sponsor
Linnaeus University
Collaborators
Vastra Gotaland Health Care Region, The Kamprad Family Foundation for Entrepreneurship, Research & Charity, Karolinska Institutet, Capio Group
1. Study Identification
Unique Protocol Identification Number
NCT05335382
Brief Title
Implementation and Evaluation of Primary Care Behavioral Health in Sweden
Acronym
KAIROS
Official Title
Implementation and Evaluation of Primary Care Behavioral Health in Sweden - A Cluster Randomized Design for Superiority and Non-superiority Comparisons of Effects on Patient Reach, Availability, Costs, Sick-leave, Model Fidelity, and Patients' Everyday Function, Symptoms, and Experiences
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Linnaeus University
Collaborators
Vastra Gotaland Health Care Region, The Kamprad Family Foundation for Entrepreneurship, Research & Charity, Karolinska Institutet, Capio Group
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In this multicenter study, the investigators want to compare treatment outcomes for patients with mental and behavioral health problems in traditional primary care (Care As Usual, CAU) and primary care centres that work according to the Primary Care Behavioral Health (PCBH) model. In addition to this, the investigators want to study organisation-level outcomes, such as access to care, perceived teamwork and work environment. To achieve this, primary care centres that have expressed interest in implementing PCBH will be cluster randomised between implementing directly or waiting for implementation.
Detailed Description
The overarching goal of primary care is to offer all patients individualised and context-sensitive healthcare with high access and continuity. One of the reasons primary care struggles with this goal is that a large proportion of patients suffer from mental and behavioural health problems, alone or in combination with one or several chronic illnesses. Despite many patients needing psychosocial interventions, there is a lack of mental health professionals as well as clear pathways for these patients.
Primary Care Behavioral Health (PCBH) is an innovative way of organising primary care, where mental health professionals have more yet shorter visits, strive for same-day access, and have an active consulting role in the primary care team. To help patients achieve relevant behavioral changes, so called brief interventions are used, which are based on isolated components from psychological treatments such as Cognitive Behavioral Therapy (CBT) and Acceptance and Commitment Therapy (ACT). Brief interventions usually stretch over 1-4 treatment sessions. Assessments within the model are generally contextual and largely avoid psychiatric diagnostics, instead focusing on the patient's situation and their associated coping strategies - whether they be positive or negative. Although PCBH is gaining in popularity, recent reviews conclude that among the evaluation trials there are very few comparative studies. As such, there is a great need for proper evaluation of a method that is already widely implemented.
Data will be collected at 17 primary care centers (PCCs) in Västra Götalandsregionen, Sweden, that have expressed an interest in implementing PCBH. The study is looking at both patient and organizational level variables. The PCCs will be randomized between implementing PCBH immediately (December 2021) or delayed with 5-9 months (implementation in late spring or early autumn of 2022). Outcome data will be collected also from the PCCs waiting for implementation, while they apply Care as Usual (CAU). Collection of patient self-ratings will start before the first implementation of PCBH to ensure functional data collection routines and possibly create a longer baseline, but the main analysis will use data from the period from when PCCs in the Early implementation arm actually have implemented PCBH to a good enough level and until PCCs in the control group start their implementation. Data from all PCCs will be continuously be collected also during the period when the delayed group implements PCBH. For individual patients, the primary end-point for the primary outcome (everyday functioning) will be 12 weeks after the first visit. Patient outcomes are also measured after 1 year.
Outcome at the organizational level will be measured in several ways, and here the primary outcome will be two measures of waiting time between identification of patient (i.e. them self-referring for mental or behavioral health issues) and the first visit: (a) actual waiting-time and (b) Outcome at the organizational level will be measured in several ways, and here the primary outcome will be two measures of waiting time between identification of patient (i.e. them self-referring for mental or behavioral health issues) and the first visit: (a) actual waiting-time for each patient identified as relevant for inclusion and (b) Third Next Available Appointment (TNAA) for the PCC as a whole, measured at the same day and time each week.
Fidelity will be measured by an expert group as well as using four questionnaires, one for each of mental health professionals, medical doctors, registered nurses and leadership. Implementation data will also be collected from these professional groups/roles at the implementing PCCs, for example with the s-NoMAD questionnaire.
During the implementation process, all psychosocial resources (all relevant psychologists, social workers, psychotherapists and so on) will be trained in the PCBH model during 3 days. The psychosocial resources are required to already be equipped with basic training in psychotherapy, for example in CBT or psychodynamic therapies. All training will be followed up with six 4-hour group supervision sessions. PCC leaders, doctors and nurses will be included in the supervision when a need to work on inter-professional issues arises and might also receive some separate, extra supervision for up till 10 h in total if necessary. In addition to this, all PCCs will go through a half-day training of all clinical personnel at the PCC, of which 2 hours is set aside with an implementation group where all professions at the PCC are represented.
The overall main research question is:
Is PCBH superior to traditional primary health care in yielding the best patient outcomes regarding level of functioning (primary outcome) and symptoms, reaching the most patients, and reducing wait-times and costs?
Secondary research questions include:
Is (1) true also for the sub-group of complex patients with somatic/mental comorbidities and social difficulties?
Is PCBH superior to traditional primary care in reducing objectively measured sick-leave? Is this, and level of functioning and symptoms, moderated by which intervention is given within PCBH? Is this true also for the sub-group of complex patients? Is this subgroup also reached by behavioral health interventions more than in traditional primary care?
Does the implementation of PCBH result in lower levels of prescribed pharmacological treatment for depression, anxiety, sleep, and pain?
What changes to group and organizational variables like teamwork, knowledge about and respect for other professions, clinical knowledge about behavior health and work environment satisfaction occur after the implementation of PCBH?
How does the level of fidelity, acceptability and implementation quality affect patient and implementation outcomes? Do these variables moderate results in all above research questions?
Which obstacles and facilitators are observed during implementation of PCBH? What factors influence fidelity and health care personnel satisfaction with PCBH?
PCBH has the potential to increase the quality and access of care for many patients with mental and behavioural health problems. This study is the first to step towards answering whether or not the effects of PCBH are large enough to merit large-scale implementation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychological Distress, Life Style Induced Illness, Life Stress, Mental Health Disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Primary care centers are cluster randomized between implementing PCBH directly or implementing later. Patients seeking care at each PCC are not individually randomized, but are given the form of care that is currently offered at their PCC (pre- or post-implementation).
Masking
ParticipantOutcomes Assessor
Masking Description
Patients will only be informed that the study is assessing the quality of primary care, and will not know that PCBH has been or will be implemented. Since primary and most secondary outcomes are patient-rated, outcomes assessors are also deemed to be blind.
Allocation
Randomized
Enrollment
666 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Implementing PCBH directly
Arm Type
Experimental
Arm Description
PCCs randomized to this arm will immediately start the implementation of PCBH.
Arm Title
Delayed implementation of PCBH
Arm Type
Active Comparator
Arm Description
PCCs randomized to this arm will have a delayed start of their PCBH implementation, waiting between 5-9 months. During this time, the same patient-level and organizational-level data will be collected from these centers while they continue to use traditional primary care / Care As Usual (CAU) .
Intervention Type
Behavioral
Intervention Name(s)
Brief Interventions (BI)
Other Intervention Name(s)
Focused CBT, Focused ACT, Focused Cognitive Behavioural Therapy, Focused Acceptance and Commitment Therapy
Intervention Description
'Brief Interventions' (BI) is a multitude of interventions used in patient visits within PCBH. BI start immediately at the initial consultation, which ends with a personally tailored and evidence-informed plan adjusted to the patient's context. The interventions within BI often have their foundation in CBT, ACT or Motivational Interviewing (MI), however interventions from other schools of therapy can also be used. The common theme is that they are principle-based rather than manual-based and focus on behavioural change in relation to a problem, rather than focusing on a specific diagnosis. Follow-up appointments are scheduled flexibly depending on the patient's perceived need. A BI treatment usually consists of 1-4 appointments with several weeks apart and has an open ending, where the patient easily can schedule a new appointment. Clinicians delivering brief interventions will have had 3 days of training as well as regular supervision.
Intervention Type
Behavioral
Intervention Name(s)
Care As Usual (CAU)
Intervention Description
Care As Usual includes the PCC's current routine care for patients with mental and behavioral problems. This can include a multitude of procedures and treatment, such as pharmacological treatment, supportive care, cognitive behavioural therapy (CBT) and psychodynamic therapy of varying lengths. Interviews with patients as well as medical journals will be used to categorise what type of care each individual patient has received.
Primary Outcome Measure Information:
Title
WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (4 domains)
Description
The eight items constituting the four domains of Life activities, Cognition, Getting along, and Participation in the 12-item version of the WHO Disability Assessment Schedule 2.0 (WHODAS-12) will be used as primary outcome, since these are condition-independent measures of Behavioral Health relevant everyday functioning. The scale ranges from 0 to 32 points. A lower score means better functioning. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, and Week 12
Title
Waiting time until first appointment
Description
Waiting time from the patient contacting their PCC with a behavioural health concern to being seen by a physician or psychosocial resource among patients in the study
Time Frame
From documented identification/self-referral to documented first visit at PCC (up to 6 months after identification)
Secondary Outcome Measure Information:
Title
WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (2 domains)
Description
The two domains of Mobility and Self-care will be measured and the whole WHODAS will be used in some secondary analyses, but not for the primary outcome since these domains tend to form two independent factors, many patients will have initial adequate function in these domains and they are not expected to change much. The scale ranges from 0 to 48 points. A lower score means better functioning. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 12 and 1 year
Title
Third next available appointment (TNAA)
Description
Waiting time until next available appointment for a third hypothetical patient that calls in on a given day for every clinician at the PCC, measured on the same time every week (e. g. Mondays at 9 AM), a measure of access to and and availability of care that is independent of patients own ability to show up at an offered time.
Time Frame
Measured each week from implementation to up to 2 years
Title
Patient Health Questionnaire 9-Item (PHQ-9)
Description
The full version of a well-validated scale for measuring depressive symptoms. PHQ-9 total score for the nine items ranges from 0 to 27. A lower score means less depressive symptoms. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 12 and 1 year
Title
Patient Health Questionnaire 2-Item (PHQ-2)
Description
PHQ-2 consists of two questions from the PHQ-9. This will be administered as part of the PHQ-9 on the above mentioned time points, and will replace the PHQ-9 on the mid-treatment measurements. The scale ranges from 0 to 6 points. A lower score means less depressive symptoms. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Generalized Anxiety Disorder 7-item (GAD-7)
Description
The full version of a well-validated scale for measuring anxiety symptoms. GAD-7 total score for the seven items ranges from 0 to 21. A lower score means less anxiety symptoms. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 12 and 1 year
Title
Generalized Anxiety Disorder 2-item (GAD-2)
Description
GAD-2 consists of two questions from the GAD-7. This will be administered as part of the GAD-7 on the above mentioned time points, and will replace the GAD-7 on the mid-treatment measurements. The scale ranges from 0 to 6 points. A lower score means less anxiety symptoms. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Social Phobia Inventory - Abbreviated version (Mini-SPIN)
Description
Social anxiety symptoms are measured with a very short version of a well established patient-rated scale for social phobia. The scale ranges from 0 to 12 points. A lower score means less symptoms of social anxiety. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
The Alcohol Use Disorders Identification Test-Concise (AUDIT-C)
Description
Symptoms of alcohol misuse are measured with a very short version of a well established patient-rated scale for alcohol misuse. The scale ranges from 0 to 12 points. A lower score means less symptoms of alcohol misuse. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Panic Disorder Severity Scale - Self rated 2-item (PDSS-SR-MINI-2)
Description
Symptoms of panic attacks are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. The scale ranges from 0 to 8 points. A lower score means less symptoms of panic disorder. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Karolinska Exhaustion Disorder Scale 3-item (KEDS-3) + 2 confirming questions from the Swedish questionnaire 'självskattat utmattningssyndrom' (s-UMS) ['self-rated burnout-syndrome']
Description
Symptoms of stress-related exhaustion are measured with a very short version of a well established patient-rated scale and has been created by an expert group, who chose three representative questions from the original KEDS scale. To aid with diagnostics, two confirmatory questions from the Swedish s-UMS scale were added, asking for duration and presumed cause of symptoms. The scale ranges from 0 to 18 points. A lower score means less symptoms of stress-related exhaustion. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Perceived Stress Scale (PSS-MINI-2) + 2 new questions
Description
Stress symptoms are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. To increase face validity of the very short scale, we also added two more direct questions ("Have you been feeling stressed lately?", "Have you been feeling tense lately?"). The scale ranges from 0 to 16 points. A lower score means less stress symptoms. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Insomnia Severity Index 2-item (ISI-MINI-2)
Description
Symptoms of sleep disorders are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. The scale ranges from 0 to 8 points. A lower score means less sleep problems. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Short Health Anxiety Inventory 3-item (SHAI-MINI-3)
Description
Symptoms of health anxiety are measured by a very short version of a well established patient-rated scale and has been created by factor analytic item-reduction and sensitivity to change analyses from large datasets from previous trial within the research group. The scale ranges from 0 to 9 points. A lower score means less symptoms of health anxiety. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Obsessive Compulsive Disorder 3-Item (OCD-3-MINI)
Description
Symptoms of obsessive compulsive disorder are measured by a very short patient-rated scale and has been created by an expert group. The scale ranges from 0 to 12 points. A lower score means less obsessive/compulsive thoughts and behaviors. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Pain One-item Rating
Description
Pain is measured on a scale from 0 to 10, where 0 is no pain and 10 is worst pain imaginable. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Total symptom index
Description
Also, a total index for level of symptoms will be calculated from all symptom items, where different weights will be used to balance the different number of questions for different domains, for example to avoid the larger number of items related to anxiety to overshadow depression ratings. The scale ranges from 0 to 20 points. A lower score means less mental health symptoms overall. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Brunnsviken Brief Quality of Life Questionnaire (BBQ)
Description
Quality of life will be measure be the 12-item Brunnsviken Brief Quality of life (BBQ-12), asking about importance and fulfilment of six areas (e.g. spare time quality, creative work, and friendship). The scale ranges from 0 to 96 points. A lower score means lower quality of life. As such, a higher score is a better outcome.
Time Frame
Change during the period Pre, Week 12 and 1 year
Title
Outcome Rating Scale (ORS)
Description
The ORS is a four-item measure designed to assess areas of life functioning known to change as a result of therapeutic intervention. These include symptom distress, interpersonal well-being, social role, and overall well-being, measured by four visual analogue scales. The scale ranges from 0 to 40 points. A lower score means lower satisfaction with life areas. As such, a higher score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Session Rating Scale (SRS)
Description
The Session Rating Scale (SRS) is a four-item visual analogue scale designed to assess key dimensions of effective therapeutic relationships. These include respect and understanding, relevance of the goals and topics, client-practitioner fit and overall alliance. The scale ranges from 0 to 40 points. A lower score means lower ratings of the therapeutic alliance. As such, a higher score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12 and 1 year
Title
Patient-rated perception and attitude toward care provider
Description
9-items previously used in PCBH-settings (self-report), and four items from the Client Satisfaction Questionnaire (CSQ). The scale ranges from 0 to 57 points. A lower score means less satisfaction with care. As such, a higher score is a better outcome.
Time Frame
Week 12
Title
Description of Behavioral Health Plan (PCBH) as structured note by clinician in medical record
Description
Interview form.
Time Frame
Week 12
Title
Patient recollection of plan/goal/methods, descriptions of behaviour changes made
Description
Interview form.
Time Frame
Week 12
Title
Experienced negative/Adverse Events, where the worst and most probably care-induced event is more thoroughly described and rated on severity and perceived cause
Description
Interview form.
Time Frame
Week 12
Title
Adverse Events-9
Description
9 items asking patients to detail any adverse events that occurred as a result of treatment.
Time Frame
Week 12
Title
Adverse Events-3
Description
3 items asking patients to detail any adverse events that occurred as a result of treatment.
Time Frame
Week 4, Week 8
Title
Well-being Behaviors
Description
11 items asking patients how often (number of days each week) they engage in behaviors related to maintaining physical and mental well-being, such as physical exercise and having adequate sleep hygiene. The first 10 items are summarized as an average where 0 is minimum and 7 is maximum. Higher scores indicate more well-being behaviors and better outcome.
Time Frame
Change during the period Pre, Week 12 and 1 year
Title
Long-term WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (4 domains)
Description
The same as Primary Outcome, but with a long-term time-frame. The scale ranges from 0 to 32 points. A lower score means better functioning. As such, a lower score is a better outcome.
Time Frame
Change during the period Pre, Week 4, Week 8, Week 12, and 1 year
Other Pre-specified Outcome Measures:
Title
Change during the period Pre, Week 12 and 1 year
Description
The Trimbos and iMTA questionnaire on Costs associated with Psychiatric Illness (TIC-P) is a validated patient-reported outcome measure concerning the utilization of medical care and productivity losses. It does not have a minimum or maximum score but collects information that is needed for doing health economic calculations. This includes outcome measures such as amount of days on sick leave, productivity loss when at work, productivity loss at home, and medications prescribed and taken. Patient self-report will be complemented with register-level data on sick leave and medications.
Time Frame
Pre, Week 12, 1 year
Title
Availability of bookable appointments
Description
Amount of bookable appointments each week per full time psychosocial resource (personnel in training counted as 75% of full time). An indirect measure of availability to psychosocial resources.
Example: A PCC have 2 full time psychosocial resources. During a week, they together have 18 bookable appointments. The "Availability of bookable appointments" of the PCC will then be 18/2 = 9.
Time Frame
Monthly from study start up to 2 years
Title
Future capacity
Description
Number of available time slots for appointments in the coming 4 weeks divided by total number of time slots in the caregiver's calendar, an indirect measure of availability
Time Frame
Monthly from study start up to 2 years
Title
Number of visits and phone / video contacts during treatment duration
Description
Average number of visits per treatment, averaged across groups
Time Frame
All visits during Pre-Week 12
Title
Percentage of patients presenting with a new primary reason for visit or more than 6 months since last visit
Description
An indirect measure of reach of psychosocial interventions
Time Frame
Pre, 6 months, 1 year
Title
The number of patients seen per full time equivalent mental health professional for at least one visit in relation to all patients listed at the PCC
Description
A measure of reach of psychosocial interventions
Time Frame
Pre, 6 months, 1 year
Title
The number of patients seen per full time equivalent mental health professional for at least one visit in relation to all patients with an ICD-10 diagnosis of F10-99, R40-45 or Z55-65
Description
A measure of reach of psychosocial interventions
Time Frame
Pre, 6 months, 1 year
Title
PCBH Fidelity: Integrated Behaviours in Primary Care - Psychosocial Resource Edition (IBPC-PSR)
Description
To measure PCBH fidelity and competence among psychosocial resources
This questionnaire, self-rated by psychosocial resources, is not yet validated and has been created by the research group, as previously existing questionnaires have been difficult to apply to the Swedish healthcare system. The questionnaires will be validated parallel to this study. The scales include subscales to measure several specific areas of interest, such as collaboration between psychosocial resources and medical personnel. Summarized as percentage of perfect Fidelity, where higher scores means better Fidelity.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
PCBH Fidelity: Levels of Integration Measure, Swedish version (S-LIM)
Description
To measure PCBH fidelity and competence among leaders of PCC:s
This questionnaire, self-rated by leaders, is not yet validated and has been created by the research group, as previously existing questionnaires have been difficult to apply to the Swedish healthcare system. The questionnaires will be validated parallel to this study. The scales include subscales to measure several specific areas of interest, such as collaboration between psychosocial resources and medical personnel. Summarized as percentage of perfect Fidelity, where higher scores means better Fidelity.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
PCBH Fidelity: Integrated Behaviours in Primary Care - Registered Nurse Edition (IBPC-RN)
Description
To measure PCBH fidelity and competence among nurses
This questionnaire, self-rated by nurses, is not yet validated and has been created by the research group, as previously existing questionnaires have been difficult to apply to the Swedish healthcare system. The questionnaires will be validated parallel to this study. The scales include subscales to measure several specific areas of interest, such as collaboration between psychosocial resources and medical personnel. Summarized as percentage of perfect Fidelity, where higher scores means better Fidelity.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
PCBH Fidelity: Integrated Behaviours in Primary Care - GP Edition (IBPC-GP)
Description
To measure PCBH fidelity and competence among General Practitioners
This questionnaire, self-rated by General Practitioners, is not yet validated and has been created by the research group, as previously existing questionnaires have been difficult to apply to the Swedish healthcare system. The questionnaires will be validated parallel to this study. The scales include subscales to measure several specific areas of interest, such as collaboration between psychosocial resources and medical personnel. Summarized as percentage of perfect Fidelity, where higher scores means better Fidelity.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
Attitudes to brief interventions
Description
The AIM-IAM-FIM measurement with the three subscales Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM) and Feasibility of Intervention Measure (FIM) to measure implementation constructs acceptability, appropriateness and feasibility of PCBH implementation. Each subscale includes 4 items rated 1-5 each subscale have thus a min of 4 and max of 20, while the total scale has a min of 12 and max of 60. Higher scores indicate better outcome.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
Implementation success of PCBH
Description
The original British instrument the Normalization Process Theory Measure (NoMAD) is based on the four core constructs of the Normalization Process Theory: Coherence, Cognitive Participation, Collective Action, and Reflexive Monitoring. They represent ways of thinking about implementation and are focused on how interventions can become part of everyday practice. The s-NoMAD is the validated Swedish version of the NoMAD. It includes 20 questions about the intervention, corresponding to the four constructs of, with Coherence and Cognitive Participation having four items each (each scale with a min of 0 and a max of 16), seven items for Collective Action (with a min of 0 and a max of 28), and five items for Reflexive Monitoring (with a min of 0 and a max of 20). Higher scores means better outcome
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
Average number of completed visits per day to psychosocial resources
Description
A measure of productivity and indirect measure of reach.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
Percentage of patients seen for more than 4 visits
Description
A measure of model fidelity and indirect measure of reach.
Time Frame
At 1 year follow-up after implementation of PCBH
Title
Number of canceled visits and no-shows
Description
A measure of model fidelity.
Time Frame
At 1 year follow-up after implementation of PCBH
Title
Percentage of patients referred to specialized care, such as psychiatry or private therapy
Description
A measure of model fidelity.
Time Frame
At 1 year follow-up after implementation of PCBH
Title
Changes in personnel turnover rates
Description
A measure of model fidelity.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
Changes in number of working days with vacant positions
Description
A measure of model fidelity.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
Changes in number of working days covered by temporary general practitioners and nurses
Description
A measure of model fidelity.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
Title
Subscales Meaning of Work, Work Life Conflict, Quality of Work, Work Engagement, Quantitative Demands and Sense of Community at Work from the Copenhagen Psychosocial Questionnaire III (COPSOQ-III)
Description
A measure of work strain. Total score summarized as an average of all items, presented as a percentage form 0% to 100% where higher scores means less strain/stress and more satisfaction/health and thus represents a better outcome.
Time Frame
At implementation of PCBH and 6 months and 1 year after that
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients from age 18 who seek care at the PCC, who are deemed to be suitable for Behavioural Health interventions and booked to the mental health professionals at the PCC, according to screening methods and/or clinical assessments made by health care personnel at the PCC, will be included. This broad criteria reflects the naturalistic setting where decisions of clinicians, rather than highly standardized criteria, are the basis for inclusion.
Exclusion Criteria:
Does not speak Swedish well enough to fill out questionnaires.
Is in need of emergency type care, like with suicidal ideation or behaviours, ongoing psychosis or mania.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anneli Farnsworth von Cederwald
Phone
+46722372300
Email
anneli.farnsworthvoncederwald@lnu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Viktor Kaldo, Professor
Organizational Affiliation
Linnaeus University, Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Närhälsan Hjällbo Vårdcentral
City
Angered
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ann Martinus
Email
ann.martinius@vgregion.se
Facility Name
Närhälsan Bollebygd Vårdcentral
City
Bollebygd
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eva Johansson
Email
eva.marg.johansson@vgregion.se
Facility Name
Närhälsan Dalsjöfors Vårdcentral
City
Dalsjöfors
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paula Olofsson Lindberg
Email
paula.olofsson.lindberg@vgregion.se
Facility Name
Närhälsan Mösseberg Vårdcentral
City
Falköping
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eva-Lisa Karlsson
Email
eva-lisa.c.karlsson@vgregion.se
Facility Name
Närhälsan Oden Vårdcentral
City
Falköping
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Agnetha Tibblin
Email
agnetha.tibblin@vgregion.se
Facility Name
Närhälsan Gråbo Vårdcentral
City
Gråbo
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Martina Bergsten
Email
martina.bergsten@vgregion.se
Facility Name
Närhälsan Eriksberg Vårdcentral
City
Göteborg
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annika Robinson
Email
annika.robinson@vgregion.se
Facility Name
Närhälsan Gibraltargatan Vårdcentral
City
Göteborg
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrik Berglund
Email
patrik.berglund@vgregion.se
Facility Name
Närhälsan Majorna Vårdcentral
City
Göteborg
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marina Halldin
Email
marina.halldin@vgregion.se
Facility Name
Närhälsan Sannegården Vårdcentral
City
Göteborg
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ulrika Fredriksson Ebbeus
Email
ulrika.ebbeus@vgregion.se
Facility Name
Närhälsan Solgärde Vårdcentral
City
Kungälv
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susanne Gustafsson
Email
susanne.gustafsson@vgregion.se
Facility Name
Närhälsan Tjörn Vårdcentral
City
Kållekärr
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ann-Sofie Lekander
Email
ann-sofie.lekander@vgregion.se
Facility Name
Närhälsan Ågårdsskogen Vårdcentral
City
Lidköping
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Dalemar
Email
maria.dalemar@vgregion.se
Facility Name
Närhälsan Mellerud Vårdcentral
City
Mellerud
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annette Johansson
Email
annette.in.johansson@vgregion.se
Facility Name
Närhälsan Munkedal Vårdcentral
City
Munkedal
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cecilia Kristmansson
Email
cecilia.kristmansson@vgregion.se
Facility Name
Närhälsan Stenungsund Vårdcentral
City
Stenungsund
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ann Sundström
Email
ann.sundstrom@vgregion.se
Facility Name
Närhälsan Källstorp Vårdcentral
City
Trollhättan
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amira Donlagic
Email
amira.donlagic@vgregion.se
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Implementation and Evaluation of Primary Care Behavioral Health in Sweden
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