Skip to main content
OpenTrials
Completed

NCT Number: NCT00949858

New Data Analysis Methods for Actigraphy in Sleep Medicine

The purpose of this study is to develop statistical and informatics tools for analyzing and visualizing Actical™ (actigraphy) data linked to fatigue in Sleep Medicine Center patients.

Completed

Looking for future studies?

Notify Me

Key information

About this study

An Actical™ is a watch-like device attached to the wrist that uses an accelerometer to measure movement nearly continuously over several days. The American Academy of Sleep Medicine practice parameters report that actigraphy is a useful tool for detecting sleep in healthy individuals, assessing specific aspects in insomnia and restless legs syndrome, circadian-rhythm disorders, and excessive sleepiness. Concurrent with these recommendations is an increased interest in the use of actigraphy as a tool for objectively measuring fatigue. With improved high-end statistical methods for analyzing this data, actigraphy has the potential to become more important as an objective diagnostic tool for determining fatigue, sleep abnormalities and assessing response to treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient presenting to the Washington University Sleep Medicine Center for evaluation of obstructive sleep apnea syndrome, restless legs syndrome, or insomnia
  • Older than 18 years of age
  • Ability to consent to participation in the study
  • Willingness to wear the Actical™ for two 7 day periods and to return the equipment promptly

Exclusion criteria

  • Inability to provide valid consent
  • Pregnancy
  • Night or rotating shift workers

Treatment and study plan

Primary outcomes

  1. Define an object oriented data model for actigraphy and patient level data.

    Time frame: 6 months

Secondary outcomes

  1. Apply existing and develop new advanced statistical and visualization methods for actigraphy data and include them in the data model listed above.

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Collaborators

  • Utah State University

Registry information

Important dates

Study start
2009
Primary completion
2014
Study completion
2014
First posted
Jul 30, 2009
Registry last updated
Jul 31, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.