Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT05977712

Circadian Rhythm and Other Factors in Memory Clinic Patients

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-02-19

1200

Participants Needed

2

Research Sites

938 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

I

Institut National de la Santé Et de la Recherche Médicale, France

Collaborating Sponsor

AI-Summary

What this Trial Is About

The CIRCAME study is a bicentric study of patients from 2 memory clinics in Paris. The main objective is to identify circadian rhythm components and other individual risk factors (sociodemographic, behavioral, and health related factors) associated with the diagnosis of subtypes (AD, Lewy bodies, vascular, frontotemporal dementia) and stages (cognitively healthy, mild cognitive impairment, clinical dementia) of dementia, independent of known risk factors (sociodemographic and genetic) and assess the relevance of use of these factors in primary care for screen of dementia including subtypes and stages. A secondary objective is to determine factors associated with progression of the disease, in terms of cognitive decline and limitations in activities of daily living, as well as progression to dementia among cognitively healthy controls and patients with mild cognitive impairment, up to 15 years after the inclusion period.

CONDITIONS

Official Title

Circadian Rhythm and Other Factors in Memory Clinic Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient of legal age (18 or over)
  • Signed informed consent form
  • Patient affiliated to the french social security system
Not Eligible

You will not qualify if you...

  • Skin allergy to plastic
  • Diagnosis of psychiatric disorder that can explain all cognitive symptoms
  • Inability to come accompanied for patients with a Mini-Mental State Examination (MMSE) cognitive score �38 or a clinician assessment indicating the need to be accompanied (e.g. wheelchair use, agitation)
  • Participation at the time of inclusion and during the 9-day period of wearing the accelerometer in interventional research with potential impact on circadian rhythm

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 2 locations

1

Centre de neurologie Cognitive / CMRR

Paris, France, France, 75010

Actively Recruiting

2

Hôpital de Jour Gériatrique et consultation mémoire

Paris, France, France, 75018

Actively Recruiting

Loading map...

Research Team

C

Claire PAQUET, MDPhD

CONTACT

S

Séverine SABIA, PhD

CONTACT

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here