Improving Physical Health in Patients With Psychiatric Disorders in General Practice (SOFIA) (SOFIA)
Primary Purpose
Psychiatric Disorder, Schizophrenia, Bipolar Disorder
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
SOFIA model
Sponsored by
About this trial
This is an interventional health services research trial for Psychiatric Disorder
Eligibility Criteria
Inclusion Criteria:
- Registered at a general practice situated in the Danish Capital Region or the Region of Zealand;
- Registered at general practice with International Classification of Primary Care version 2 (ICPC-2) diagnostic code p72 (psychotic disorders);
- Registered at general practice with ICPC-2 diagnostic code p73 (bipolar mood disorders);
- Prescription of Lithium (Anatomical Therapeutic Chemical (ATC): N05AN);
- Registered at general practice with ICPC-2 diagnostic code p76 AND (Prescription of Lamotrigine (N03A09) OR Carbamazepine (N03AF01) OR Valproic Acid (N03AG01));
- Registered at general practice with ICPC-2 diagnostic code p76 (unipolar depressive disorders) AND (Prescription of tricyclic antidepressants (N06AA) AND/OR venlafaxine (N06AX16) AND/OR duloxetine (N06AX21) AND/OR Monoamine Oxidase A Inhibitor (MAOi) (N06AG) AND/OR non-selective MAOi (N06AF)).
Exclusion Criteria:
- Subjected to any type of legal measure as stipulated in the Danish Mental Health Law;
- Registered with a dementia diagnosis ICPC-2 p70 (dementia);
- Receiving end-of-life care;
- Non-Danish speakers;
- Assumed by the patient's general practitioner to have an overall functional level that is too low for meaningful participation in trial.
Sites / Locations
- University of Copenhagen
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Coordinated, co-produced health care
Care as usual
Arm Description
Care as usual
Outcomes
Primary Outcome Measures
Effectiveness of the design in terms of recruitment of practices and patients
Proportion of contacted general practices, which agree to participate in the study and the eligibility and consent rate of patients.
Acceptability of the intervention for patients and general practitioners, staff and patients.
Qualitative semi-structured interviews with patients and general practitioners, staff and patients.
Retention of patients during the study
Proportion of recruited patients in the intervention group who attend the first consultation.
Acceptability of REDcap software for general practitioners
Qualitative semi-structured interviews with general practitioners.
Effectiveness of the collecting Multimorbidity Questionnaires
Proportion of returned and completed Multimorbidity Questionnaires.
Effectiveness of the collecting EQ5D-5L questionnaires
Proportion of returned and completed EQ5D-5L questionnaire.
Mortality
Number of all-cause deaths of participants during the 6 month trial period.
Hospitalizations
Number of all-cause in- and outpatient hospitalizations of participants during the 6 months trial period.
Secondary Outcome Measures
Multimorbidity Questionnaires (MMQ) scores
Scores on Multimorbidity Questionnaire
Full Information
NCT ID
NCT04618250
First Posted
October 26, 2020
Last Updated
April 26, 2022
Sponsor
University of Copenhagen
1. Study Identification
Unique Protocol Identification Number
NCT04618250
Brief Title
Improving Physical Health in Patients With Psychiatric Disorders in General Practice (SOFIA)
Acronym
SOFIA
Official Title
A Cluster Randomized, Pilot Trial of Coordinated, Co-produced Care to Reduce Excess Mortality and Improve Quality of Life in Patients With Severe Mental Illness in General Practice Setting
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
November 6, 2020 (Actual)
Primary Completion Date
September 30, 2021 (Actual)
Study Completion Date
September 30, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Copenhagen
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
People with a severe mental illness (SMI) have an increased risk for premature mortality, predominantly due somatic health conditions. Evidence indicates that prevention and improved treatment of somatic conditions in patients with SMI could reduce this excess mortality. This paper reports a protocol designed to evaluate the feasibility and acceptability of a coordinated co-produced care programme (SOFIA model) in the general practice setting to reduce mortality and improve quality of life in patients with severe mental illness. The primary outcomes are description of study feasibility (recruitment and retention) and acceptability.
The SOFIA trial is designed as cluster randomized controlled trial targeting general practices in two regions in Denmark. 12 practices will each recruit 15 community-dwelling patients aged 18 and older with severe mental illness (SMI). Practices will be randomized in a ratio 2:1 to deliver a coordinated care program or care-as-usual during a 6 month period. An online randomized algorithm is used to perform randomization. The coordinated care program comprises enhanced educational training of general practitioners and their clinical staff, and prolonged consultations focusing on individual needs and preferences of the patient with SMI. Assessments are administered at baseline, and at end of study period.
If delivery of the intervention in the general practice setting proves feasible, a future definitive trial to determine the effectiveness of the intervention in reducing mortality and improving quality of life in patients with SMI can take place.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychiatric Disorder, Schizophrenia, Bipolar Disorder, Severe Depression
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
76 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Coordinated, co-produced health care
Arm Type
Experimental
Arm Title
Care as usual
Arm Type
No Intervention
Arm Description
Care as usual
Intervention Type
Other
Intervention Name(s)
SOFIA model
Intervention Description
A mandatory two day course for general practitioners assigned to the intervention group A prolonged consultation at the general practitioner Use of an individual care plan
Primary Outcome Measure Information:
Title
Effectiveness of the design in terms of recruitment of practices and patients
Description
Proportion of contacted general practices, which agree to participate in the study and the eligibility and consent rate of patients.
Time Frame
6 months after randomization
Title
Acceptability of the intervention for patients and general practitioners, staff and patients.
Description
Qualitative semi-structured interviews with patients and general practitioners, staff and patients.
Time Frame
Entire study period (6 months)
Title
Retention of patients during the study
Description
Proportion of recruited patients in the intervention group who attend the first consultation.
Time Frame
6 months after randomization
Title
Acceptability of REDcap software for general practitioners
Description
Qualitative semi-structured interviews with general practitioners.
Time Frame
Entire study period (6 months)
Title
Effectiveness of the collecting Multimorbidity Questionnaires
Description
Proportion of returned and completed Multimorbidity Questionnaires.
Time Frame
6 months after randomization
Title
Effectiveness of the collecting EQ5D-5L questionnaires
Description
Proportion of returned and completed EQ5D-5L questionnaire.
Time Frame
6 months after randomization
Title
Mortality
Description
Number of all-cause deaths of participants during the 6 month trial period.
Time Frame
6 months after randomization
Title
Hospitalizations
Description
Number of all-cause in- and outpatient hospitalizations of participants during the 6 months trial period.
Time Frame
6 months after randomization
Secondary Outcome Measure Information:
Title
Multimorbidity Questionnaires (MMQ) scores
Description
Scores on Multimorbidity Questionnaire
Time Frame
3 times during study period (at baseline, before prolonged consultation and 6 months after randomization
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Registered at a general practice situated in the Danish Capital Region or the Region of Zealand;
Registered at general practice with International Classification of Primary Care version 2 (ICPC-2) diagnostic code p72 (psychotic disorders);
Registered at general practice with ICPC-2 diagnostic code p73 (bipolar mood disorders);
Prescription of Lithium (Anatomical Therapeutic Chemical (ATC): N05AN);
Registered at general practice with ICPC-2 diagnostic code p76 AND (Prescription of Lamotrigine (N03A09) OR Carbamazepine (N03AF01) OR Valproic Acid (N03AG01));
Registered at general practice with ICPC-2 diagnostic code p76 (unipolar depressive disorders) AND (Prescription of tricyclic antidepressants (N06AA) AND/OR venlafaxine (N06AX16) AND/OR duloxetine (N06AX21) AND/OR Monoamine Oxidase A Inhibitor (MAOi) (N06AG) AND/OR non-selective MAOi (N06AF)).
Exclusion Criteria:
Subjected to any type of legal measure as stipulated in the Danish Mental Health Law;
Registered with a dementia diagnosis ICPC-2 p70 (dementia);
Receiving end-of-life care;
Non-Danish speakers;
Assumed by the patient's general practitioner to have an overall functional level that is too low for meaningful participation in trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susanne Reventlow
Organizational Affiliation
University of Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Copenhagen
City
Copenhagen
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Participants' study information will not be released outside of the study without the written permission of the participant.
Citations:
PubMed Identifier
34479646
Citation
Rozing MP, Jonsson A, Koster-Rasmussen R, Due TD, Brodersen J, Bissenbakker KH, Siersma V, Mercer SW, Guassora AD, Kjellberg J, Kjellberg PK, Nielsen MH, Christensen I, Bardram JE, Martiny F, Moller A, Reventlow S; SOFIA Study Group. The SOFIA pilot trial: a cluster-randomized trial of coordinated, co-produced care to reduce mortality and improve quality of life in people with severe mental illness in the general practice setting. Pilot Feasibility Stud. 2021 Sep 3;7(1):168. doi: 10.1186/s40814-021-00906-z.
Results Reference
derived
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Improving Physical Health in Patients With Psychiatric Disorders in General Practice (SOFIA)
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