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A Study of Wrist Actigraphy in Overweight and Obese Adults With Sleep Disorders

S

Shanghai Jiao Tong University School of Medicine

Status

Completed

Conditions

Sleep Disorders

Treatments

Device: Wrist Actigraphy(motion sensors)with light sensors-Jawbone Up 2

Study type

Observational

Funder types

Other

Identifiers

NCT02260297
CCEMD-023

Details and patient eligibility

About

70 overweight or obese adults with sleep disorders will be recruited for this study, in which the investigators aim to compare wrist actigraphy with polysomnography (PSG) for sleep monitoring. It is to evaluate the applications of Jawbone Up2 with the sleep parameters derived from this actigraphy.

Full description

As an observation study, it will recruit 70 overweight or obese patients with sleep disorders who meet the selection criteria: clinical records and AIS at a tertiary hospital. The patients will sign the informed consent form. The involved patients and doctors will receive related training.

These patients will receive the sleep monitoring from 21:00 to 6:00 in sleep monitoring laboratory in Ruijin Hospital. They will receive the PSG and Jawbone Up 2 sleep monitoring at the same time. Sleep parameters derived from actigraphy and PSG will be compared in multiple night recordings such as total sleep time, wake after sleep onset, sleep onset latency, awakening, sleep efficiency, total time in bed,. The aim is to assess the validation of actigraphy in overweight or obese patients with sleep disorders.

Enrollment

69 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Have one or more sleep disorders such as consecutive snoring, insomnia, sleep apnea, narcolepsy, delayed sleep phase syndrome
  • Athens Insomnia Scale (AIS)>6
  • BMI>25
  • Agree to participate in the study and have signed the inform consent form

Exclusion criteria

  • Terminal illness
  • Physically-challenged and paralyzed patients
  • Intend to receive selective surgery, to get pregnancy and breast feeding in three months
  • Long-term use of the sleeping pills
  • Hearing loss or severe visual disorder;
  • Mental disorders
  • Dementia or communication disorders
  • Unable to complete an all night sleep monitoring

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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