- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03508518
Improving Access to Psychiatric Care for Patients in Primary Care (DSPP-PSY)
Improving Access to Psychiatric Care and the Fluidity of Care Pathways for Patients Suffering From Mental Disorders in Primary Care in France: Evaluation of a Psychiatric Consultation-liaison System
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Faced with the saturation of the psychiatric care system, who recognizes the key role of the GP in mental health. Three-quarters of prescriptions for antidepressants and anxiolytics are performed by GPs, but less than one in four people with depression have been diagnosed and treated appropriately. The GPs describe difficulties in accessing psychiatric professionals and in particular to obtain a quick consultation with a psychiatrist. In different countries, psychiatric consultation-liaison (CL), centered on the collaboration of general medicine and psychiatry, have emerged. Two meta-analyzes and a Cochrane review were conducted on CL but no clinical trials were conducted in France. CL seems to improve patients' health at 3 months as well as their satisfaction and adherence to care. Results regarding the improvement of prescriptions from GP are encouraging. Better clinical trials are being requested and a need for medico-economic studies is also identified.
In France, a psychiatry CL was born in Toulouse in 2017, the "DSPP". The present study plans a 2 groups randomized clinical trial, one group of GPs having access to DSPP, the other not. For a period of 3 months, the GPs propose to any patient, for whom they want a psychiatric consultation, to participate in the study and address him/her to a psychiatrist. The DSPP is an evaluation center without long-term patient follow-up. Only patient referred by his/her GP can get into the DSPP.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Toulouse, France, 31059
- University Hospital Toulouse
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 15 years patient or older:
- presenting mental suffering or a frequent or severe mental disorder
- having consulted his GP who ask for psychiatric consultation
- having given its consent for the use of its medico-administrative data
- affiliated with the general health insurance scheme
- of which the GP is from Haute Garonne and is voluntary to participate in the study
- Free, informed and written consent signed by the participant and the investigator (at the latest on the day of inclusion and before any examination required by the research) and by one of the parents for minor participants
Exclusion Criteria:
- Patient with ongoing psychiatric follow-up
- Patient unable to answer questionnaires (unable to read or write)
- Patients receiving a measure of legal protection
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Shared care device in psychiatry (DSPP)
System focused on collaboration between general medicine (GP) and psychiatry, offering psychiatric assessment consultations and guidance for patient addressed by his/her GP.
Referrals are made to the GP with support for care or the patient can be oriented to routine psychiatric care.
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The GPs of the intervention group will be able to refer their patients to the DSPP or to the routine care.
The patient has a nursing telephone interview prior to one or few more psychiatric consultations.
The time to obtain the psychiatric consultation is measured into the 2 groups.
In both groups, questionnaires will be sent to the patient and their medico-administrative data will be collected passively over a period of 6 months after inclusion
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Active Comparator: Care as usual
Patient will have usual care : Psychiatric care available in the Haute Garonne: psychiatric consultation by a liberal psychiatrist or by a psychiatrist working in public health center |
psychiatric care available in the Haute Garonne: psychiatric consultation by a liberal psychiatrist or by a psychiatrist working in public health center.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Number of patients who had access to a consultation with a psychiatrist
Time Frame: 2 to 21 working days after inclusion
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Number of patients who had access to a consultation with a psychiatrist within 2 working days following the GP consultation for patients whose GP wishes an "urgent" consultation, within 7 working days for a "quick" consultation and within 21 working days for a "non-urgent" consultation.
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2 to 21 working days after inclusion
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of days between M0 (GP consultation) and M1 (psychiatric consultation)
Time Frame: 6 months
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Number of days between M0 (GP consultation) and M1 (psychiatric consultation) collected passively on the bases of Health Insurance, Information Systems Medicalization Program (PMSI) and DSPP
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6 months
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Number of passages to psychiatric emergencies
Time Frame: 6 months
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Number of passages to psychiatric emergencies within 6 months M0 passively collected on the basis of the PMSI (Information Systems Medicalization Program) of psychiatric emergencies
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6 months
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Number of suicide attempts
Time Frame: 6 months
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Number of suicide attempts and suicides within 6 months following M0 passively collected on the basis of the PMSI of the psychiatric emergencies and the Health Insurance
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6 months
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Mental health status by Symptom Checklist (SCL)
Time Frame: date of inclusion, 1 month and 6 months after inclusion
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Mental health status measured at M0, 1 month and 6 months by questionnaires hand-delivered by the GP at M0 and sent at 1 and 6 months : - SCL-90-R scale: Scale exploring 9 symptomatic dimensions (somatization, obsession-compulsion, sensory traits, depression, anxiety, hostility, phobic anxiety, paranoid ideals, psychotic traits) by Likert scale in 5 points. Passing 15min. |
date of inclusion, 1 month and 6 months after inclusion
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Mental health status by Patient Health Questionnaire (PHQ)
Time Frame: date of inclusion, 1 month and 6 months after inclusion
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Mental health status measured at M0, 1 month and 6 months by questionnaires hand-delivered by the GP at M0 and sent at 1 and 6 months : - the PHQ-9 scale for the diagnosis of major depressive episode and the intensity of depression. 9 questions are rated from 0 to 3 by the patient, ie a score of severity ranging from 0 to 27. |
date of inclusion, 1 month and 6 months after inclusion
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Duration of prescription of different drugs
Time Frame: date of inclusion, 1 month and 6 months after inclusion
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Duration of prescription of a benzodiazepine, antidepressant, hypnotic and antipsychotic treatment passively collected on the bases of Health Insurance
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date of inclusion, 1 month and 6 months after inclusion
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Evaluation of compliance with antidepressant prescriptions
Time Frame: date of inclusion, 1 month and 6 months after inclusion
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Composite criterion for the evaluation of compliance with antidepressant prescriptions including drug type (first-line serotonin reuptake inhibitors (IRS): 0 or 1) and duration (6 months minimum: 0 or 1) with a total score of 0 to 2
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date of inclusion, 1 month and 6 months after inclusion
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Number of prescription treatment of mental disorders
Time Frame: date of inclusion, 1 month and 6 months after inclusion
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Number of prescription of a benzodiazepine, antidepressant, hypnotic and antipsychotic treatment passively collected on the bases of Health Insurance
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date of inclusion, 1 month and 6 months after inclusion
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Employment status
Time Frame: 6 months
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Occupation, without profession (Number and duration of sick leave within 6 months following M0, passively collected on the bases of Health Insurance)
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6 months
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Patient satisfaction
Time Frame: 1 month
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Patient satisfaction measured at 1 month of M0 by the Client Satisfaction Questionnaire (CSQ-8 scale)
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1 month
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Quality of life with EuroQol scale
Time Frame: 6 months
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Quality of life measured by the EuroQol (EQ-5D-5L) scale at M0 and 6 months by a clinical researcher by phone The EQ-5D-5L scale consists of 2 pages, a descriptive system EQ-5D and a visual analogue scale EQ .
The descriptive system explores the following five dimensions: mobility, autonomy, usual activities, pain / discomfort and anxiety / depression.
Each dimension is rated in 5 levels .
The visual analogue scale is a vertical scale where the endpoints are labeled "best health imaginable" and "worst health imaginable"
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6 months
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GP satisfaction
Time Frame: 6 months
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GP satisfaction measured by questionnaire
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6 months
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Incremental Cost-Utility
Time Frame: 6 months
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to determine Incremental Cost-Utility collected passively on the bases of Health Insurance, PMSI and DSPP
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6 months
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Cost-Effectiveness Ratios of Patient Management Strategies
Time Frame: 6 months
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to determine Cost-Effectiveness Ratios of Patient Management Strategies collected passively by data on the bases of Health Insurance, PMSI and DSPP
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6 months
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Production costs
Time Frame: 6 months
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to determine production costs collected passively on the bases of Health Insurance, PMSI and DSPP
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6 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Sophie Prébois, MD, University Hospital, Toulouse
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC31/17/0357
- 2017-A03127-46 (Other Identifier: ID-RCB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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