← Back to Clinical Trials
Recruiting NCT06738784

NCT06738784 Evaluation of the Efficiency of the PRPP (Perceive, Recall, Plan and Perform) Task Analysis System on Support and Orientation Decisions for People With Aging Psychiatric Disorders (PATPV) Living in Independent Housing.

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06738784
Status Recruiting
Phase
Sponsor Centre Hospitalier Charles Perrens, Bordeaux
Condition Mental Health
Study Type INTERVENTIONAL
Enrollment 66 participants
Start Date 2024-12-09
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 40 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Perceive, Recall, Plan and Perform (PRPP) evaluation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 66 participants in total. It began in 2024-12-09 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Over the past 30 years, mental health policy has been geared towards increasing the number of people receiving care in the community, with a reduction of over 50% in the number of general psychiatric beds. The WHO recommends the implementation of alternatives to hospitalization, through the development of outpatient and home-based psychiatric care programs that support independent living. People suffering from psychiatric disorders show cognitive decline as they age, including deficits in perception, attention, memory and problem-solving. These cognitive problems affect the ability to carry out the tasks of daily life, and make it more difficult to remain at home. In order to avoid hospitalization for these psychiatrically-stabilized patients who are losing their autonomy, it is necessary to take into account their mental and cognitive handicap, and to provide them with appropriate compensation. Occupational therapy is a discipline concerned with the assessment, rehabilitation and integration of people with disabilities. Occupational therapists provide ecological assessments to support personalized care plans. The PRPP (Perceive, Recall, Plan and Perform) task analysis system is a validated, ecological tool that integrates an occupational therapy assessment and intervention model. The PRPP assessment measures occupational performance and the impact of cognitive impairments on information processing and on the cognitive strategies required to carry out activities. Research conducted in Canada illustrates the value of PRPP in supporting people with schizophrenia. To the best of our knowledge, no team has studied the use of PRPP in the decision-making process for maintaining people with aging psychiatric disorders (PATPV) at home.

Eligibility Criteria

Inclusion Criteria: * Be at least 40 years old * Reside within the PGU sector (Mérignac, Pessac, Talence and Gradignan) * Receive support from the PGU - CHCP "pathologies, disability and aging" department. * Fluency in French Exclusion Criteria: * Being hospitalized for more than 18 months * Refuse inclusion in the research project

Contact & Investigator

Central Contact

Julie BONVALLET

✉ jbonvallet@ch-perrens.fr

📞 05.33.57.80.23

Frequently Asked Questions

Who can join the NCT06738784 clinical trial?

This trial is open to participants of all sexes, aged 40 Years or older, up to 65 Years, studying Mental Health. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06738784 currently recruiting?

Yes, NCT06738784 is actively recruiting participants. Contact the research team at jbonvallet@ch-perrens.fr for enrollment information.

Where is the NCT06738784 trial being conducted?

This trial is being conducted at Bourdeaux, France.

Who is sponsoring the NCT06738784 clinical trial?

NCT06738784 is sponsored by Centre Hospitalier Charles Perrens, Bordeaux. The trial plans to enroll 66 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology