Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06852326

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

Led by University Hospital, Tours · Updated on 2025-02-28

30

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are designing a tailored primary care intervention to help manage the challenges faced by people caring for patients with Alzheimer's disease or related dementias. The study uses a two-phase process: first, reaching consensus on the intervention through expert panels using a Delphi-modified method, and second, assessing how acceptable the developed intervention is to carers and healthcare professionals. This approach follows guidelines for developing complex interventions and involves collaboration among carers, healthcare workers, and academic experts. The first phase involves several rounds where panels rate proposed interventions via questionnaires and discussions until a consensus is reached, typically after 3-4 rounds. The second phase introduces the agreed-upon intervention to three professional health communities, collecting both quantitative data on usage and acceptance, and qualitative feedback through observations and interviews. This ongoing evaluation allows the intervention to be refined continuously. Participants include adult informal carers, healthcare professionals from the involved communities, and university experts. Data collection involves qualitative interviews, focus groups, and surveys to measure how well the intervention is accepted and used over time. The main outcome is a detailed description of the intervention after 12 months, with acceptability assessed at 6 months. The study spans multiple months and follows a structured process for developing and evaluating the intervention.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthcare professionals who are members of the three participating territorial professional health communities (CPTSs) and agree to participate
  • Adult informal carers of patients living with Alzheimer's disease or related dementia from the three CPTSs who agree to participate
  • University experts including general practitioners, geriatric mobile team doctors, advanced practice nurses, clinical psychologists, and biostatistical methodologists who agree to participate
Not Eligible

You will not qualify if you...

  • Professional carers

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.

1 screening and enrollment visit

Delphi Rounds for Intervention Design

Duration - Several weeks, typically 3 to 4 rounds

Participants engage in multiple rounds of rating and discussion to develop and refine a tailored primary care intervention for managing caregiving burden. This involves completing questionnaires and attending meetings to discuss and validate intervention proposals.

Multiple remote questionnaire rounds and panel meetings

Acceptability Assessment

Duration - 6 months

Participants provide feedback through qualitative interviews, focus groups, and observations to assess the acceptability of the designed intervention. Quantitative data on intervention uptake, refusal, and abandonment will also be collected.

Periodic qualitative interviews and focus groups

Ongoing Intervention Evaluation and Adaptation

Duration - Up to 12 months

The intervention may be adapted continuously based on ongoing feedback from participants and stakeholders throughout the study period, ensuring relevance and acceptability.

Ongoing engagement through interviews, focus groups, and observations

Trial Site Locations

Total: 3 locations

1

CPTS Asclepios

Amboise, France, 37400

Actively Recruiting

2

CPTS Pays d'Iroise

Saint-Renan, France, 29290

Not Yet Recruiting

3

CPTS Est Cher

Sancergues, France, 18140

Actively Recruiting

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Research Team

C

Clarisse DIBAO-DINA, Pr

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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