Development of a Model for Shared Care in the Interface Between General Practice and Mental Health Care

August 21, 2022 updated by: Michael Haurum Marcussen, Psychiatric Research Unit, Region Zealand, Denmark

Development of a Model for Shared Care in the Interface Between General Practice and Mental Health Care - a Co-production Study

Recent research has underlined that mental health of people with depression and anxiety has deteriorated over the last decades in Denmark as well as internationally, and has reached a degree where it is perceived as a global health challenge. By now, depression is the most common reason for early retirement on health grounds in Denmark. Early intervention in relation to patients with depression and anxiety is essential, as research further shows that many young people with mental health difficulties drop out of education and work. The overall purpose is to develop a shared care intervention in co-production with users, and to increase their recovery by strengthening the support and treatment using a newly developed shared care model.

The study is designed as a non-randomized intervention study with a control group. Comparative analyzes will be performed with pre- and post-assessments. Patients will be recruited between August 2022 and February 2023. The patients are referred to outpatient clinics based on their home address. The two outpatient clinics should be comparable in terms of patients' diagnoses and staffing. ward. Mental health status and well-being are the primary outcomes. Self-reported questionnaires will be administered to both groups before and after the intervention.

The study will be approved by the Research Ethical Committee of University of Southern Denmark and Region Zealand. The study findings will be published in peer-reviewed journals and presented at national and international conferences.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

Background Recent research has underlined that mental health of people with depression and anxiety has deteriorated over the last decades in Denmark as well as internationally, and has reached a degree where it is perceived as a global health challenge. Depression and anxiety affect individuals' psychosocial well-being and occupational functioning and are increasing causes of sick leave in high-income countries. By now, depression is the most common reason for early retirement on health grounds in Denmark. Early intervention in relation to patients with depression and anxiety is essential, as research further shows that many young people with mental health difficulties drop out of education and work. Yet it appears that people with mental health difficulties do not receive adequate and sufficient support and treatment. Even though Shared Care between general practice and mental health service was initiated in Denmark more than 10 years ago, the collaboration between the two sectors continues to be challenged. Nonetheless, general practice remains central for the course of treatment of anxiety and depression as the majority of people with these disorders are diagnosed and treated in the primary sector. Among international researchers, there is consensus that most patients should continue to be treated in general practice, however the treatment could be optimized through strengthened collaboration between general practice and mental healthcare services. There is an increasing recognition that improving the treatment and outcomes for people with mental health problems requires service models that integrate mental healthcare within primary healthcare practice. Shared care enables a 'best of both worlds' scenario with the opportunity to provide holistic care of high quality to support the recovery process of people with mental health difficulties. Shared care should lead to pooling of expertise and enhanced creativity in problem-solving. It should also decrease the number of patients 'left in limbo' between primary and secondary sector, with patients and carers feeling that they are failing to make progress through the healthcare system. The most recent Cochrane systematic review of the evidence base for shared care (2013) concluded that shared care interventions significantly improve treatment outcomes compared to treatment as usual. In a situation where researchers, patients and policymakers continue to push for the adoption of shared care between general practice and mental health service, and bearing in mind that the most recent review is almost ten years old, we find that a systematic review of recent studies of shared care is timely, notably to provide a synthesis of the best available evidence for recommendations for future shared care interventions. There is also a great desire for a high degree of user involvement in the project, partly for the purpose of learning for all parties involved, and furthermore to strengthen implementation. Involving users in the study will enhance our understanding of stakeholders' perspectives in relation to their support, treatment, and recovery process. However, there is a lack of stakeholder involvement in this type of research. The project follows Psychiatry in Region Zealand's overall strategy for implementing Recovery, on the assumption that a shared cared approach strengthens the treatment and the social support, and thereby supports the recovery process of people with mental illness. The overall purpose is to develop a shared care intervention in co-production with users, and to increase their recovery by strengthening the support and treatment using a newly developed shared care model.

Methods A systematic review (Step 1) is followed by an explanatory study (Step 2) with interviews of relevant stakeholders in shared care to explore how general practitioners, mental health staff and patients perceive collaboration, user involvement and the course of treatment in shared care. Both steps are planned to inform and qualify an intervention (Step 3). It is the assumption that the involvement of patients in all phases will result in a higher relevance for both clinical practice and patients (ref.). Therefore, we have decided to create a new Shared Care intervention that will be developed in co-production with the users. Co-production in research is defined as "an approach in which researchers, practitioners and the public work together, sharing power and responsibility from the start to the end of the project, including the generation of knowledge." (NIHR 2021).

Step 1 - Systematic review A systematic review is conducted based on the following research questions 1) What characterizes a shared care model? 2) how do general practitioners, mental health providers, and patients experience shared care? The review is planned and will be implemented and published based on PRISMA guidelines. We will conduct a search in the following databases: Medline, CINAHL, PsychINFO and EMBASE for both qualitative and quantitative studies, published in the period January 2001 to January 2022. Two independent researchers will conduct screening on both title and abstract level (MM and BN). Furthermore, full-text reading and quality assessment (risk of bias) will be based on CASP checklists. The project is registered in Prospero (287989) and carried out through the software platform covidence.org.

Step 2 - Perspectives on shared care This study is intended to supplement Step 1 (systematic review) with a user perspective (both people with mental illness and health professionals) on shared care. Phase 2 will be an exploratory study based on interviews with people involved in shared care in Region Zealand, general practitioners, patients, as well as health professionals from the mental health service. The interviews will be conducted to investigate what people with mental illness and health professionals find important in the pathways as well as their perspectives on shared care, collaboration, and recovery. Informants will be found with a view to maximal variation in terms of age, sex, profession, diagnosis, and duration of illness. A semi-structured interview guide will be prepared and data analysis will be based on thematic analysis, inspired by Kvale & Brinkmann and Coffey & Atkinson.

This study is based on the two previous steps, including a systematic review (ID: 287989) and an exploration of users' experiences of shared care - collaboration between general practice and mental healthcare. Both steps are planned to inform and qualify the intervention but no further described in this protocol.

Study design The study is designed as a non-randomized intervention study with a control group. Comparative analyzes will be performed with pre- and post-assessments. Patients will be recruited between August 2022 and February 2023. The patients are referred to outpatient clinics based on their home address. The two outpatient clinics should be comparable in terms of patients' diagnoses and staffing. The trial is registered in ClinicalTrials.gov (NCT not yet assigned) and adhered to the Consort guidelines.

Intervention The Shared Care model consists of the following key elements: Shared care is a collaboration between general practice and mental health services and enables a 'best of both worlds' scenario with the opportunity to provide holistic care of high quality to support the recovery process of people with mental health difficulties. The final version of the intervention can only be determined based on the results of the research steps 1+2.

Study population The participants are adults aged 18 - 65 years, diagnosed with depression and anxiety, and referred to outpatient clinics in Region Zealand.

Procedure for recruitment Data collection via questionnaires, which will be administered to the patients at the first visit in the outpatient clinic and after 3 months. Patients who did not consent to participation or failed to complete the questionnaire at the first visit in the outpatient-clinic were excluded from the study.

Primary outcome Mental health status is valid and reliable indicator of the patients self-reported mental state and well-being. Mental status is assessed using the standardized Short Form Health Survey (SF-36), first developed in the US by Ware and Sherbourne. A Danish translation of the original English-language version will be used.

Secondary outcomes The patients level of function is assessed using the Global assessment of functioning (GAF), and their satisfaction is measured with the client satisfaction score scale (CSQ-8) and the quality of Life enjoyment and satisfaction questionnaire (Q-LES-Q (SF). The patients' recovery will be assessed by the 24-item recovery assessment scale-revised (RAS-R). All scales have been validated in a Danish population. The implementation of the Shared Care model will be ensured by fidelity assessments. Checklists will be used to ensure that the collaborative meetings are held as planned.

Sample size The sample size calculation is based on an intervention study with SF-36 as the primary outcome, also conducted in Mental health services. In this study, there is a clinically relevant effect size 0.5 with a power 80 ((α = 0.05). Based on this study's sample size calculation, 120 patients in each group are needed (intervention and control).

Ethical considerations Information of participants and data management will be planned in accordance with the Helsinki Declaration. Informed consent based on information, both written and verbally, about the aim, purpose and use of the study and the data collection will be obtained from all participants. Furthermore, all participants will be informed that their participation was voluntary, that they could withdraw their consent at any time without consequences, and that their statements would be treated confidentially and anonymized. Data will be entered into the EasyTrial © Online Clinical Trial Management system. All personal identifiers will be removed or disguised during analysis to preclude personal identification. The project will be reported to the Danish Data Protection Agency and the Region Zealand Ethics Committee.

Study Type

Interventional

Enrollment (Anticipated)

240

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Out patient
  • Diagnosed with: Anxiety and Depression
  • Aged 18 - 65 years

Exclusion Criteria:

  • Cognitive deficit
  • Patients who did not consent to participation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: The Shared Care model - intervention group
The patients are referred to outpatient clinics based on their home address. The two outpatient clinics should be comparable in terms of patients' diagnoses and staffing. The Shared Care model consists of the following key elements: Shared care is a collaboration between general practice and mental health services and enables a 'best of both worlds' scenario with the opportunity to provide holistic care of high quality to support the recovery process of people with mental health difficulties. The final version of the intervention can only be determined based on the results of the research steps 1+2.
The Shared Care model consists of the following key elements: Shared care is a collaboration between general practice and mental health services and enables a 'best of both worlds' scenario with the opportunity to provide holistic care of high quality to support the recovery process of people with mental health difficulties.
No Intervention: Treatment as usual - Control group
The patients are referred to outpatient clinics based on their home address. The two outpatient clinics should be comparable in terms of patients' diagnoses and staffing. In the control group the patients will receive treatment as usual.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Mental Health Status
Time Frame: At baseline and after 3 months
Mental health status is valid and reliable indicator of the patients self-reported mental state and well-being. Mental status is assessed using the standardized Short Form Health Survey (SF-36). Its 36 items are grouped into eight domains. The summed scores for each of the eight domains were plotted on a scale from 0 (worst) to 100 (best), with higher scores indicating better health
At baseline and after 3 months
Change in mental health recovery
Time Frame: Baseline and after 3 months.
The patients' recovery will be assessed by the 24-item recovery assessment scale-revised (RAS-R) - a questionnaire. It is a self-report instrument measuring mental health recovery. The RAS-R thus consists of 24 items on five-level scales. These items can be added up to produce summary scales representing five dimensions of personal recovery.
Baseline and after 3 months.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in level of function
Time Frame: Baseline and after 3 months.
The patients level of function is assessed using the Global assessment of functioning (GAF) - a questionnaire. The GAF is a scale from 0 to 100 where higher scores indicate greater levels of functioning.
Baseline and after 3 months.
Change in Patient Satisfaction
Time Frame: Baseline and after 3 months.

Satisfaction is measured with the client satisfaction score scale (CSQ-8) - a questionnaire.

  • For overall score, sum item responses, range from 8-32, higher score indicates higher satisfaction.
Baseline and after 3 months.
Change in Patient Satisfaction
Time Frame: Baseline and after 3 months.
The Quality-of-Life Enjoyment and Satisfaction Questionnaire.
Baseline and after 3 months.
Improvement in collaboration between general practice and mental health
Time Frame: Baseline and after 3 months.
The Collaborative Practice Scale.
Baseline and after 3 months.
Improvement in collaboration between general practice and mental health
Time Frame: Baseline and after 3 months.
Shared Decision-Making Questionnaire (SDM-Q9).
Baseline and after 3 months.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Michael Marcussen, Dr., University of Southern Denmark (SDU), Denmark

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

January 1, 2023

Primary Completion (Anticipated)

February 28, 2023

Study Completion (Anticipated)

December 31, 2023

Study Registration Dates

First Submitted

November 11, 2021

First Submitted That Met QC Criteria

December 27, 2021

First Posted (Actual)

December 29, 2021

Study Record Updates

Last Update Posted (Actual)

August 24, 2022

Last Update Submitted That Met QC Criteria

August 21, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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