Alzheimer's Disease Trial, Recruiting
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:
- You must be 18 years old or older
- You must be willing and able to sign a consent form agreeing to take part
- You must be registered with the French social security system
Who may not be able to join:
- You cannot take part if you have a skin allergy to plastic
- You cannot take part if you have been diagnosed with a psychiatric condition that fully explains any memory or thinking problems you have
- You cannot take part if you have significant cognitive (thinking or memory) difficulties and are unable to come to appointments with someone accompanying you, or if your doctor feels you need someone with you (for example, if you use a wheelchair or experience agitation) (confirm with trial site)
- You cannot take part if you are already involved in another research study that could affect your body clock, either at the time of joining or during the 9-day period when you would be wearing a movement-tracking device
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.
Contact this trial
Phone: 0140054313
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
Where this trial is recruiting
Primary endpoints
Dementia subtypes and stages (% at inclusion); Dementia subtypes and stages (incidence); Alzheimer's disease stages (%); Alzheimer's disease stages (change in)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.