Validation of the Actiwatch for older people with intellectual disability; a feasibility study

Completed

• Conditions: normal sleep; sleep problem; 10040998

• Registration Number: NL-OMON35404
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 10

Inclusion Criteria

- at least 50 years of age
- intellectual disability
- competent to provide informed consent
- 5 participants with a known sleep problem
- 5 participatns without a sleep problem

Exclusion Criteria

- active epilepsy
- behaviour problems that negatively influence the measurement
- not able to give informed consent themselves

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Feasibility of performing home sleep EEG registrations, together with a<br /><br>Actiwatch measurement, in older people with intellectual disability. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Sensitivity, specificity and accuracy of two different types of Actiwatch<br /><br>compared to sleep registratrion (for the low, medium, high and auto sensitivity<br /><br>setting)<br /><br>Differences between the sleep parameters Total Sleep Time, Sleep Efficiency,<br /><br>Sleep Onset Latency, Wake After Sleep Onset (for the low, medium, high and auto<br /><br>sensitivity setting)</p><br>