Actigraphy Sleep Parameters in Obstructive Sleep Apnea Patient's

Hospital Clinic of Barcelona106 enrolled

Overview

Those patient's that come to the sleep unit and that accept to participate in the study will undergo a polysomnography with the extra of an actigraphy placed in their no dominant arm wrist. The outcomes that will be analyzed are: Time in bed, assumed sleep time, wake time, sleep efficiency, sleep latency, light's on/light's off

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

106

Conditions

Obstructive Sleep Apnea

Interventions

PolysomnographyDEVICE

Patient's undergo a polysomnography

ActigraphyDEVICE

Patient's wear an actigraphy while doing the polysomnography

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patient's with OSA suspicion undergoing a PSG in the sleep unit Exclusion Criteria: * Neurologic disorders * Severe comorbidities * Other sleep disorders, such as insomnia * No informed consent

Locations (1)

Hospital Clinic

Barcelona, Spain

Outcomes

Primary Outcomes

Sleep time (min)

To compare the outcomes acquired with the actigraphy with those acquired by the Polysomnography

Time frame: 3 months

Secondary Outcomes

sleep efficiency

To evaluate the agreement, sensitivity and specificity between the outcomes acquired by the Polysomnography and by the actigraphy.

Time frame: 3 months

Wake time

To evaluate the agreement, sensitivity and specificity between the outcomes acquired by the Polysomnography and by the actigraphy.

Time frame: 3 months

sleep latency

To evaluate the agreement, sensitivity and specificity between the outcomes acquired by the Polysomnography and by the actigraphy.

Time frame: 3 months

Data from ClinicalTrials.gov

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