RecruitingNCT05977712

Circadian Rhythm and Other Factors in Memory Clinic Patients

Circadian Rhythm and Other Individual Factors Among Memory Clinic Patients


Sponsor

Assistance Publique - Hôpitaux de Paris

Enrollment

1,200 participants

Start Date

Mar 6, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This observational study is examining how sleep-wake rhythms (circadian rhythms) and other lifestyle factors relate to memory and cognitive decline in patients attending a memory clinic. Participants wear a wristband activity tracker for 9 days. **You may be eligible if...** - You are 18 or older - You are a patient attending a memory clinic in France - You are covered by the French social security system - You are able to attend with a companion if your memory score is low **You may NOT be eligible if...** - You have a skin allergy to plastic (the wristband material) - You have a psychiatric disorder that fully explains all your cognitive symptoms - You are participating in another interventional research study that affects sleep or circadian rhythm - You cannot come to appointments accompanied, if required Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERQuestionnaire

The questionnaire includes information on socio-demographics (age, sex, education, occupation, marital status), behavioural (smoking, alcohol consumption, social functioning), and health-related factors (morbidities, treatment, sleep disturbance, eye diseases, frailty, falls).

OTHERClinical examination

This includes earing test, cognitive tests (mini-mental status examination, MemScreen), body mass index, waist circumference, blood pressure and blood tests (biomarkers of Alzheimer's disease, neurodegeneration, and other dementias).

OTHERAccelerometer port

Participants will be wearing an accelerometer for 9 days.

OTHEREye examination

Eye fundus photo, OCT and OCT-A exams

OTHEREar Examination

Otoscopic examination, Wideband tympanometry, Pure-tone and speech audiometry (in quiet and in noise), Auditory evoked potentials, Electroencephalogram with auditory stimulation


Locations(2)

Centre de neurologie Cognitive / CMRR

Paris, France, France

Hôpital de Jour Gériatrique et consultation mémoire

Paris, France, France

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NCT05977712


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