Actively Recruiting
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
Eligibility Criteria
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
You will not qualify if you...
- Professional carers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
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
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
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
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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