Alzheimer's Disease Trial, Recruiting NCT05516667 Sponsor: University Hospital, Toulouse Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT05516667
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

Alzheimer's disease (AD) patients:

  • People who have been diagnosed with probable Alzheimer's disease, confirmed through recognised clinical and biological criteria
  • People with mild to moderate Alzheimer's disease, based on a standard memory and thinking test score of 15 or above (out of 30)
  • People who are fluent enough in French to complete study questionnaires
  • People who agree to attend medical check-ups at the start of the study, and again at 12 and 24 months
  • People who are enrolled in the French social security system
  • People who give written consent to participate

Caregivers:

  • People who assist an AD patient with daily activities for at least 6 hours per week over the past 6 months, where that patient has also agreed to take part in the study
  • People aged 18 or older
  • People who are fluent enough in French to complete study questionnaires
  • People who agree to regularly fill in questionnaires about their own health or the AD patient's health, either during visits, online, or by post
  • People who are enrolled in the French social security system
  • People who give written consent to participate

First-degree relatives (such as parents, children, or siblings of an AD patient):

  • People who are a first-degree relative of an AD patient who has also agreed to take part in the study
  • People aged 18 or older
  • People who are fluent enough in French to complete study questionnaires
  • People who agree to attend medical check-ups at the start of the study, and again at 12 and 24 months
  • People who agree to regularly fill in questionnaires about their own health, either online or by post
  • People who are enrolled in the French social security system
  • People who give written consent to participate

Group structure requirement:

  • The study requires a family group of 2 to 5 people: either 1 AD patient and 1 first-degree relative who also acts as their caregiver, OR 1 AD patient, 1 caregiver (who does not need to be a relative), and between 1 and 3 first-degree relatives of the patient

Who may not be able to join:

AD patients:

  • People who have another brain condition in addition to Alzheimer's disease
  • People whose Alzheimer's disease is caused by a directly inherited (autosomal dominant) genetic form of the condition
  • People who are under a legal protection arrangement, such as guardianship or a similar measure
  • People who are currently living in a care home or institution
  • People whose life expectancy is less than 2 years

Caregivers:

  • People who are under a legal protection arrangement, such as guardianship or a similar measure
  • People who have been diagnosed with a serious condition affecting memory and thinking (major neurocognitive disorder)

First-degree relatives:

  • People whose family member has an inherited (autosomal dominant) form of dementia
  • People who carry a known gene mutation linked to inherited dementia
  • People who are under a legal protection arrangement, such as guardianship or a similar measure
  • People who have been diagnosed with a serious condition affecting memory and thinking (major neurocognitive disorder)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Sandrine Andrieu, MD, University Hospital, Toulouse

Phone: 05 61 14 59 63

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
6 April 2023
Est. completion
1 June 2026

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Recruitment rate; Retention rate

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov