DSPP-PSY: Improving Access to Psychiatric Care for Patients in Primary Care

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Recruiting
CT.gov ID
NCT03508518
Collaborator
Ministry of Health, France (Other)
240
1
2
65.1
3.7

Study Details

Study Description

Brief Summary

Getting a consultation with a psychiatrist within an appropriate time is one of the main issues reported by general practitioners (GP) for patients suffering from mental disorders in primary care. Consultation liaison in psychiatry is a system focused on general medicine-psychiatry collaboration. The aim of the present study is to evaluate the impact of the consultation-liaison on the adequacy of the access time to a psychiatric consultation according to the degree of urgency evaluated by the GP.

Condition or Disease Intervention/Treatment Phase
  • Other: Shared care device in psychiatry (DSPP)
  • Other: Usual Care
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
240 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
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
Actual Study Start Date :
Aug 28, 2018
Anticipated Primary Completion Date :
Feb 28, 2023
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
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.

Other: Shared care device in psychiatry (DSPP)
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

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

Other: Usual Care
psychiatric care available in the Haute Garonne: psychiatric consultation by a liberal psychiatrist or by a psychiatrist working in public health center.

Outcome Measures

Primary Outcome Measures

  1. Number of patients who had access to a consultation with a psychiatrist [2 to 21 working days after inclusion]

    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.

Secondary Outcome Measures

  1. Number of days between M0 (GP consultation) and M1 (psychiatric consultation) [6 months]

    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

  2. Number of passages to psychiatric emergencies [6 months]

    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

  3. Number of suicide attempts [6 months]

    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

  4. Mental health status by Symptom Checklist (SCL) [date of inclusion, 1 month and 6 months after inclusion]

    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.

  5. Mental health status by Patient Health Questionnaire (PHQ) [date of inclusion, 1 month and 6 months after inclusion]

    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.

  6. Duration of prescription of different drugs [date of inclusion, 1 month and 6 months after inclusion]

    Duration of prescription of a benzodiazepine, antidepressant, hypnotic and antipsychotic treatment passively collected on the bases of Health Insurance

  7. Evaluation of compliance with antidepressant prescriptions [date of inclusion, 1 month and 6 months after inclusion]

    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

  8. Number of prescription treatment of mental disorders [date of inclusion, 1 month and 6 months after inclusion]

    Number of prescription of a benzodiazepine, antidepressant, hypnotic and antipsychotic treatment passively collected on the bases of Health Insurance

  9. Employment status [6 months]

    Occupation, without profession (Number and duration of sick leave within 6 months following M0, passively collected on the bases of Health Insurance)

  10. Patient satisfaction [1 month]

    Patient satisfaction measured at 1 month of M0 by the Client Satisfaction Questionnaire (CSQ-8 scale)

  11. Quality of life with EuroQol scale [6 months]

    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"

  12. GP satisfaction [6 months]

    GP satisfaction measured by questionnaire

  13. Incremental Cost-Utility [6 months]

    to determine Incremental Cost-Utility collected passively on the bases of Health Insurance, PMSI and DSPP

  14. Cost-Effectiveness Ratios of Patient Management Strategies [6 months]

    to determine Cost-Effectiveness Ratios of Patient Management Strategies collected passively by data on the bases of Health Insurance, PMSI and DSPP

  15. Production costs [6 months]

    to determine production costs collected passively on the bases of Health Insurance, PMSI and DSPP

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Toulouse Toulouse France 31059

Sponsors and Collaborators

  • University Hospital, Toulouse
  • Ministry of Health, France

Investigators

  • Principal Investigator: Sophie PrĂ©bois, MD, University Hospital, Toulouse

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Toulouse
ClinicalTrials.gov Identifier:
NCT03508518
Other Study ID Numbers:
  • RC31/17/0357
  • 2017-A03127-46
First Posted:
Apr 25, 2018
Last Update Posted:
Mar 16, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Toulouse
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 16, 2022