Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06014125

Tele-education in Patients With a Moderate Depressive Episode in Primary Care

Led by University Hospital, Toulouse · Updated on 2026-05-12

220

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying a new tele-education program for adults experiencing moderate depressive episodes. This study focuses on patients managed by their general practitioners in primary care, aiming to improve medication adherence, reduce relapse risk, and enhance patient and professional satisfaction. The program addresses a gap in France, where no psycho-education has been evaluated for this population outside psychiatric care. It uses telemedicine to adapt to recent healthcare changes, especially due to the pandemic. Participants are randomly assigned to either a tele-education program or standard care. The tele-education includes five weekly sessions, each about 60 minutes, covering personalized information on depression symptoms, treatment, diet, coping strategies, and support from family and friends. The final session summarizes what was learned and shares it with the patient’s general practitioner. The control group receives usual care plus an educational booklet on depression. During the study, participants will be monitored by their general practitioner and may also see a psychologist. They will complete questionnaires to assess medication adherence six months after joining and evaluate the tele-education's effectiveness three months after inclusion. The study includes ongoing support, with psychiatrists available for advice if needed, and focuses on improving daily functioning and treatment compliance over time.

CONDITIONS

Brief Title

Paramedical Tele-education on Moderate Depressive Episodes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Presenting a depressive episode of moderate intensity according to the Diagnostic and Statistical Manual (DSM)-V
  • Have a prescription for an antidepressant started less than 2 months before joining the trial
  • Health status compatible with follow-up by their general practitioner
  • Have internet access at home with a computer and ability to use the digital platform
Not Eligible

You will not qualify if you...

  • Unable to complete self-questionnaires due to language barrier or other reasons
  • Already participated in a psycho-education or therapeutic education program for depression
  • Health status requiring follow-up by a psychiatrist

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

screening and enrollment visit

Treatment

Duration - 5 weeks

Participants in the experimental group will receive a tele-education program consisting of 5 weekly individual sessions focusing on depression symptoms, health and diet measures, illness destigmatization, family and social support, treatment information, and session summaries. Participants in the control group will continue their usual care and receive an educational booklet on depression.

5 weekly sessions (remote)

Follow-up

Duration - Up to 6 months post inclusion

Participants may be monitored by their general practitioner or psychologist, with questionnaires completed to assess medication adherence and effectiveness of the tele-education up to 6 months after inclusion.

Questionnaire assessments at 3 and 6 months post inclusion

Trial Site Locations

Total: 1 location

1

Chu Toulouse

Toulouse, Occitanie, France, 31000

Actively Recruiting

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Research Team

M

Marion LASSERRE, NURSE

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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