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Recruiting NCT06852326

NCT06852326 Designing a Tailored Primary Care Intervention to Manage the Burden of Caring for Patients Living with Alzheimer's Disease (or a Related Dementia)

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Clinical Trial Summary
NCT ID NCT06852326
Status Recruiting
Phase
Sponsor University Hospital, Tours
Condition Primary Care
Study Type OBSERVATIONAL
Enrollment 30 participants
Start Date 2024-11-21
Primary Completion 2026-05

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

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

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 30 participants in total. It began in 2024-11-21 with a primary completion date of 2026-05.

⚠ 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

The design of the intervention is an ongoing process which will consist of two phases: a determination of the intervention using the Delphi-modified consensus method and an assessment of its acceptability, as described in the methodological recommendations of the Medical Research Council Guidance.

Eligibility Criteria

Inclusion Criteria: * Healthcare professionals who are members of the 3 CPTSs included and who agree to participate * Adult informal carers of patients living with Alzheimer's disease or a related dementia from the 3 CPTS who agree to participate * University experts: general practitioners, geriatric mobile team doctor, advanced practice nurse, clinical psychologist, biostatistical methodologist. Some of them had already taken part in the steering committee for ISAMA's exploratory qualitative and quantitative studies. Exclusion Criteria: \- Professional carers

Contact & Investigator

Central Contact

Clarisse DIBAO-DINA, Pr

✉ clarisse.dibao-dina@univ-tours.fr

📞 02 47 36 60 19

Frequently Asked Questions

Who can join the NCT06852326 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Primary Care. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06852326 currently recruiting?

Yes, NCT06852326 is actively recruiting participants. Contact the research team at clarisse.dibao-dina@univ-tours.fr for enrollment information.

Where is the NCT06852326 trial being conducted?

This trial is being conducted at Amboise, France, Saint-Renan, France, Sancergues, France.

Who is sponsoring the NCT06852326 clinical trial?

NCT06852326 is sponsored by University Hospital, Tours. The trial plans to enroll 30 participants.

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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: April 2026  ·  Data Methodology