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Patient-driven Internet Delivered Psychological Treatment

Primary Purpose

Anxiety Disorders and Symptoms, Internet-Based Intervention

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Patient-driven iCBT
Standardized iCBT (TAU)
Sponsored by
Vastra Gotaland Region
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Disorders and Symptoms

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Has reached the age of 18
  • Has access to a computer with internet connection
  • Speak and understand Swedish
  • Meets the diagnostic criteria for an anxiety disorder (social anxiety, GAD (Generalized Anxiety Disorder), panic disorder, obsessive-compulsive disorder or unspecified anxiety disorder)

Exclusion Criteria:

  • has started medication for mental illness or made major changes regarding the medication during the past 4 weeks
  • has serious suicidal thoughts or suicidal plans
  • has complex comorbidity or is in need of other care for mental illness in addition to iCBT
  • is receiving other psychological treatment during the treatment period

Sites / Locations

  • Department of Psychology, University of Gothenburg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Patient-driven iCBT

Standardized iCBT (TAU)

Arm Description

Participants who are randomized to the experimental condition are asked to make choices regarding the structure of their treatment program

Patients who are randomized to the control condition undergo the usual iCBT program available for anxiety disorders for a standardized time period of 8 weeks

Outcomes

Primary Outcome Measures

Questions of perceptions in how much one has been able to control the treatment
Perceptions in how much one has been able to control the treatment is measured by a questionnaire developed by the researchers for this study. The questionnaire consists of 9 items and each item is answered on a seven-point scale, from "Not at all" to "To a large extent".
Adherence to treatment
Adherence to treatment is measured by counting number of completed modules in the treatment program for each participant

Secondary Outcome Measures

Changes in feelings of empowerment
Empowerment is measured with the Empowerment Scale (Rogers, Chamberlin, Ellison & Crean, 1997). The scale consists of 28 items which are answered on a four-point likert scale. Score ranges between 28 and 112. Higher scores indicates that the person feels more empowered.
Perceptions of being able to cope with one's mental illness
Perceptions of being able to cope with one's mental illness is measured with the Patient Enablement Instrument (PEI; Howie, Heaney & Maxwell, 1997). The instrument consists of 6 items and are graded on a three-point scale. Score ranges between 0-12, with higher score indicating higher patient enablement.
Satisfaction with treatment
Satisfaction with treatment is measured by The Client Satisfaction Questionnaire- 8 item version (CSQ-8; Attkisson & Greenfield, 1998). The questionnaire consists of 8 items and are graded on a four-point scale. Scores ranges from 8-32, with higher scores indicating higher satisfaction.
Changes in Anxiety symptoms
Anxiety is measured with the GAD-7 instrument (Generalized Anxiety Disorder 7 item scale). The scale consists of 7 items. The score ranges from 0 to 21, with higher scores indicating more anxiety symptoms. There are thresholds for mild, medium and severe anxiety (Spitzer, Kroenke, Williams & Löwe 2006).
Changes in Depressive symptoms
Symptoms of depression is measured with Madrs-s (Montgomery Åsberg Depression Rating Scale; Montgomery & Åsberg, 1979). The instrument consists of 9 items. Scores ranges from 0 to 60, with higher scores indicating more depressive symptoms. There are cut-off points for symptom severity.
Changes in General disabillity
General disability is measured with the 12-item version of the generic assessment tool WHO Disability Assessment Schedule (WHODAS 2.0; Rhem, Ustun, Saxena, Nelson, Chatterji, Ivis & Adlaf, 1999). Scores range from 12-60, with a higher score indicating higher disability. The instrument has established normative data.
Changes in steps towards "valued direction"
Steps towards "valued direction" is measured with "the Bull´s Eye Values Survey" (Lundgren, Louma, Dahl, Strohsal & Melin, 2012).
10. Questions about how much one has been affected by the pandemic of Covid-19
Perceptions about how much one has been affected by the pandemic of Covid-19 is measured by a questionnaire developed by the researchers for this study. The questionnaire consists of 7 items that is answered on a seven-point scale. 1 indicating= To a very large extent for the worse; 4= not at all / not relevant; 7= to a very large extent for the better.

Full Information

First Posted
December 17, 2020
Last Updated
April 28, 2023
Sponsor
Vastra Gotaland Region
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1. Study Identification

Unique Protocol Identification Number
NCT04688567
Brief Title
Patient-driven Internet Delivered Psychological Treatment
Official Title
Patient-driven Internet Delivered Psychological Treatment in a Primary Care Context: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
March 30, 2021 (Actual)
Study Completion Date
March 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vastra Gotaland Region

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The effect of iCBT for adults with anxiety disorders is well-known. However, drop-out rates are common. In recent years more focus has been directed to the importance of patients being active agents in their own care and to increase the patient´s involvement in health care. Studies show that involving patients´ in treatment decisions and management of their own health care can contribute to better treatment outcomes and more appropriate use of health care service. Few studies have evaluated patient involvement in iCBT-treatment. This study aims to evaluate the effect of patient-driven iCBT-treatment for patients with anxiety disorders seeking primary care in a randomized controlled trial. The study investigates the effect of patient-driven iCBT treatment of perceptions of being able to control the treatment and on drop-out from treatment. In addition, secondary research questions investigate measures of empowerment, anxiety and depression symptoms, general disability, satisfaction with treatment and feelings of being able to cope with one's mental illness in patient-driven iCBT.
Detailed Description
The following research questions will be examined: Primary research questions: Is there a difference between participants in patient-driven digital psychological treatment, compared to standardized internet CBT, in perceptions of how much they've been able to control their treatment (measured with a questionnaire developed by the researchers for this study)? What is the effect of patient-driven digital psychological treatment, compared to standardized internet CBT, on frequency of completers and completed modules among adults with anxiety disorders? Secondary research questions: What is the effect of patient-driven digital psychological treatment, compared to standardized internet CBT, on the experience of empowerment, (measured by the "Empowerment Scale"), for adults with anxiety disorders? What is the effect of patient-driven digital psychological treatment, compared to standardized internet CBT, on anxiety (measured with GAD-7), depression (measured with MADRS-S), general disability (measured with WHODAS 2.0) and steps in "valued direction" (measured with "Bull´s Eye compass") for adults with anxiety disorders? Associations: Is there a correlation between perceptions of how much one has been able to control the treatment (measured with a questionnaire developed by the researchers for this study), feelings of being able to cope with one's mental illness (measured with Patient Enablement Instrument), how satisfied participants are with their treatment (measured vid CSQ-8), perceptions of empowerment (measured with the "Empowerment Scale") and changes in anxiety symptoms (measured with GAD-7)? Does perceptions of how much participants have been affected by the pandemic of Covid-19 in their daily life correlate with anxiety symptoms (measured with GAD-7) 3 months after termination of treatment? Mediation: What is the mediating effect of empowerment, measured by the "Empowerment Scale", on changes in anxiety symptoms (measured with GAD-7)?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Disorders and Symptoms, Internet-Based Intervention

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
The groups are predetermined based on the tool randomizer.org and blinded to the researcher assigning the participants to groups.
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patient-driven iCBT
Arm Type
Experimental
Arm Description
Participants who are randomized to the experimental condition are asked to make choices regarding the structure of their treatment program
Arm Title
Standardized iCBT (TAU)
Arm Type
Active Comparator
Arm Description
Patients who are randomized to the control condition undergo the usual iCBT program available for anxiety disorders for a standardized time period of 8 weeks
Intervention Type
Behavioral
Intervention Name(s)
Patient-driven iCBT
Intervention Description
1) Participants who are randomized to the experimental condition are asked to make choices regarding the structure of their treatment by the time of the randomization call. The participant can choose which of the available treatment programs (targeting anxiety, worry, stress, sleep disorders or depression) they want to undergo, how many modules in the treatment program they want to complete and in what order, for how many weeks they want to complete the treatment as well as how much telephone contact and how much written contact they want to have with their therapist.
Intervention Type
Behavioral
Intervention Name(s)
Standardized iCBT (TAU)
Intervention Description
2) Patients who are randomized to the control condition (standardized iCBT) undergo the usual iCBT program available for anxiety disorders for 8 weeks. The psychologist provide weekly feedback on the patient's exercises and interact with the patient via secure encrypted messages in the treatment program. A follow-up telephone call takes place at the middle of treatment and at the end of the treatment.
Primary Outcome Measure Information:
Title
Questions of perceptions in how much one has been able to control the treatment
Description
Perceptions in how much one has been able to control the treatment is measured by a questionnaire developed by the researchers for this study. The questionnaire consists of 9 items and each item is answered on a seven-point scale, from "Not at all" to "To a large extent".
Time Frame
At the end of treatment (after 8-16 weeks depending on treatment condition)
Title
Adherence to treatment
Description
Adherence to treatment is measured by counting number of completed modules in the treatment program for each participant
Time Frame
At the end of treatment (after 8-16 weeks depending on treatment condition)
Secondary Outcome Measure Information:
Title
Changes in feelings of empowerment
Description
Empowerment is measured with the Empowerment Scale (Rogers, Chamberlin, Ellison & Crean, 1997). The scale consists of 28 items which are answered on a four-point likert scale. Score ranges between 28 and 112. Higher scores indicates that the person feels more empowered.
Time Frame
Baseline (Pre-treatment), Middle of treatment, At the end of treatment (after 8-16 weeks depending on treatment condition) and by 3 months follow up
Title
Perceptions of being able to cope with one's mental illness
Description
Perceptions of being able to cope with one's mental illness is measured with the Patient Enablement Instrument (PEI; Howie, Heaney & Maxwell, 1997). The instrument consists of 6 items and are graded on a three-point scale. Score ranges between 0-12, with higher score indicating higher patient enablement.
Time Frame
At the end of treatment (after 8-16 weeks depending on treatment condition) and by 3 months follow up
Title
Satisfaction with treatment
Description
Satisfaction with treatment is measured by The Client Satisfaction Questionnaire- 8 item version (CSQ-8; Attkisson & Greenfield, 1998). The questionnaire consists of 8 items and are graded on a four-point scale. Scores ranges from 8-32, with higher scores indicating higher satisfaction.
Time Frame
At the end of treatment (after 8-16 weeks depending on treatment condition) and by 3 months follow up
Title
Changes in Anxiety symptoms
Description
Anxiety is measured with the GAD-7 instrument (Generalized Anxiety Disorder 7 item scale). The scale consists of 7 items. The score ranges from 0 to 21, with higher scores indicating more anxiety symptoms. There are thresholds for mild, medium and severe anxiety (Spitzer, Kroenke, Williams & Löwe 2006).
Time Frame
Baseline (Pre-treatment), Middle of treatment, At the end of treatment (after 8-16 weeks depending on treatment condition) and by 3 months follow up
Title
Changes in Depressive symptoms
Description
Symptoms of depression is measured with Madrs-s (Montgomery Åsberg Depression Rating Scale; Montgomery & Åsberg, 1979). The instrument consists of 9 items. Scores ranges from 0 to 60, with higher scores indicating more depressive symptoms. There are cut-off points for symptom severity.
Time Frame
Baseline (Pre-treatment), middle of treatment, At the end of treatment (after 8-16 weeks depending on the treatment condition) and by 3 months follow up
Title
Changes in General disabillity
Description
General disability is measured with the 12-item version of the generic assessment tool WHO Disability Assessment Schedule (WHODAS 2.0; Rhem, Ustun, Saxena, Nelson, Chatterji, Ivis & Adlaf, 1999). Scores range from 12-60, with a higher score indicating higher disability. The instrument has established normative data.
Time Frame
Baseline (Pre-treatment), Middle of treatment, At the end of treatment (after 8-16 weeks depending on treatment condition) and by 3 months follow up
Title
Changes in steps towards "valued direction"
Description
Steps towards "valued direction" is measured with "the Bull´s Eye Values Survey" (Lundgren, Louma, Dahl, Strohsal & Melin, 2012).
Time Frame
Baseline (Pre-treatment), Middle of treatment, At the end of treatment (after 8-16 weeks depending on treatment condition) and by 3 months follow up
Title
10. Questions about how much one has been affected by the pandemic of Covid-19
Description
Perceptions about how much one has been affected by the pandemic of Covid-19 is measured by a questionnaire developed by the researchers for this study. The questionnaire consists of 7 items that is answered on a seven-point scale. 1 indicating= To a very large extent for the worse; 4= not at all / not relevant; 7= to a very large extent for the better.
Time Frame
By 3 months follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Has reached the age of 18 Has access to a computer with internet connection Speak and understand Swedish Meets the diagnostic criteria for an anxiety disorder (social anxiety, GAD (Generalized Anxiety Disorder), panic disorder, obsessive-compulsive disorder or unspecified anxiety disorder) Exclusion Criteria: has started medication for mental illness or made major changes regarding the medication during the past 4 weeks has serious suicidal thoughts or suicidal plans has complex comorbidity or is in need of other care for mental illness in addition to iCBT is receiving other psychological treatment during the treatment period
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Linnea Nissling, Phd-student
Organizational Affiliation
Department of Psychology, University of Gothenburg, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martin Kraepelien, PhD
Organizational Affiliation
Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, Sweden
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Viktor Kaldo, Professor
Organizational Affiliation
Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, Sweden
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Dominique Hange, Docent
Organizational Affiliation
General Medicine, School of Public Health and Community Medicine, Sahlgrenska Academy, Sweden
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Anna Larsson, Psy M
Organizational Affiliation
Research, Development, Education and Innovation, Primary Health Care, Region Västra Götaland,Sweden
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sandra Weineland, Docent
Organizational Affiliation
Department of Psychology, University of Gothenburg, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Psychology, University of Gothenburg
City
Gothenburg
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We will share the data if a corresponding author or otherwise authorized person asks for it
Citations:
PubMed Identifier
34603972
Citation
Nissling L, Kraepelien M, Kaldo V, Hange D, Larsson A, Persson M, Weineland S. Effects of patient-driven iCBT for anxiety in routine primary care and the relation between increased experience of empowerment and outcome: A randomized controlled trial. Internet Interv. 2021 Sep 21;26:100456. doi: 10.1016/j.invent.2021.100456. eCollection 2021 Dec.
Results Reference
derived

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Patient-driven Internet Delivered Psychological Treatment

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