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Use of a Monitor in ME/CFS

N

New York CFS Association

Status

Unknown

Conditions

Chronic Fatigue Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT01908036
FITBIT2

Details and patient eligibility

About

The use of an activity monitor to determine increase or decrease of activity in patients suffering from chronic fatigue syndrome.

Full description

A cohort of 50 patients suffering from chronic fatigue syndrome will be given an informed release form. Have a signed the informed release they will be given a Fitbit activity monitor. These monitors will be evaluated on a weekly interval by computer interface. The activity will be calculated to determine the online of activity and whether there is increase or decrease in activity during the time of the study. The study is an observational rather than an interventional study. There is no invasion or intervention in the patient's normal activities

Enrollment

50 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Fukuda and Canadian consensus criteria for the diagnosis of chronic fatigue syndrome

Exclusion criteria

Acute disease and exclusion conditions in Fukuda criteria

Trial contacts and locations

1

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Central trial contact

derek enlander, MD

Data sourced from clinicaltrials.gov

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