Individual psychoeducation program for inpatients with schizophrenia
Official title: Evaluation of the Individual Early Psychoeducation Program for Schizophrenic Disorders in Inpatients: A Randomized, Multicenter Trial
Run by University Hospital, Tours · NCT05329363 · Data updated 2026-11-12
This study is testing a new education program for hospitalized patients with schizophrenia to see if it helps them understand their treatment better and stay well longer.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | University Hospital, Tours Academic / other |
| Locations | 11 sites (Blois and 10 other locations) |
| Status | Recruiting |
| Started | June 17, 2022 |
| Main results expected | June 2026 |
| Study ends | June 2027 |
| Registry record updated | April 23, 2024 |
| Trial ID | NCT05329363 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 to 65 with a diagnosed schizophrenic disorder or related conditions who can communicate verbally.
✕Probably not a fit
Patients who do not speak French or have participated in a psycho-education group in the last two years may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates an individual psychoeducation program called PEPITS for inpatients diagnosed with schizophrenia and related disorders. The program is designed to be implemented by nurses during the early stages of hospitalization, aiming to enhance medication compliance and improve patient insight. By focusing on psychoeducation, the study hypothesizes that it will reduce relapse rates and enhance the overall quality of life for patients. The approach emphasizes the importance of therapeutic alliance and patient engagement in their treatment.
Why it matters
Potential benefit: If successful, this program could significantly improve medication adherence and reduce relapse rates in patients with schizophrenia.
How similar studies have gone: Previous studies have shown that psychoeducation can improve treatment outcomes in psychiatric disorders, suggesting that this approach may be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age between 18 and 65 years * Patient with a diagnosed and reported schizophrenic disorder announced : * Schizophrenia * Schizoaffective disorder * Or a diagnosed and reported Delusional Disorder * Express written consent by the participant after receiving information about the study * Be able to communicate verbally * Participant affiliated to a social security scheme Exclusion Criteria: * Pregnant or breastfeeding woman * Patient who does not speak French * Participation in a psycho-education group in the last 2 years * Patient under legal protection or guardianship
Where it's running
-
Service de psychiatrie
Chinon, France Recruiting -
Service de psychiatrie
La Roche-sur-Yon, France Recruiting -
Service de psychiatrie
Rennes, France Recruiting -
Service de psychiatrie
Sainte-Gemmes-sur-Loire, France Recruiting -
Service de psychiatrie
Tours, France Recruiting -
Serrvice de Psychiatrie
Blois, France Withdrawn
Show 5 more locations
-
Service de psychiatrie
Dreux, France Not yet recruiting -
Service de psychiatrie
Fleury-les-Aubrais, France Withdrawn -
Service de psychiatrie
Neuilly-sur-Marne, France Not yet recruiting -
Service de psychiatrie
Saint-Maurice, France Not yet recruiting -
Service de psychiatrie
Sotteville-lès-Rouen, France Not yet recruiting
Study contacts
- Study coordinator: Arnaud CHESSE
- Email: A.CHESSE@chu-tours.fr
- Phone: +33(0)2.34.37.89.68
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Using Lumateperone to improve motivation in patients with schizophrenia and psychosis
This study is testing if Lumateperone can help people with schizophrenia or schizoaffective disorders feel more motivated and less apathetic.
-
Examining the effects of combined therapy for schizophrenia
This study is testing whether combining two therapies, one for managing thoughts and another for improving cognitive skills, can help people with schizophrenia do better in their daily lives compared to using just one of the therapies.
-
XEP527 in stable schizophrenia: safety and how it behaves in the body
This small, early-stage study tests the safety and how XEP527 behaves in people with stable schizophrenia who are on a single antipsychotic.
-
Theta-Burst Transcranial Magnetic Stimulation for Treatment-Resistant Auditory Hallucinations
This study tests whether theta-burst transcranial magnetic stimulation can lessen persistent auditory verbal hallucinations in adults with schizophrenia-spectrum or psychotic disorders who have not responded to antipsychotic meds.
-
Quality of life and safety in quetiapine use for schizophrenia or bipolar disorder
This study looks at how patients with schizophrenia or bipolar disorder feel and stay safe when treated with quetiapine alone or with other antipsychotics.
-
Neuronavigated rTMS for treatment-resistant auditory hallucinations
We are testing whether personalized neuronavigated inhibitory rTMS can reduce persistent auditory verbal hallucinations in adults who don’t respond to medication.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.