- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03120039
Measuring Upper Extremity Functional Movement With Accelerometry: FitBit® vs Actigraph®
April 13, 2017 updated by: Veronica Rowe, Rowe, Veronica, M.D.
Measuring Upper Extremity Functional Movement With Accelerometry: FitBit vs Actigraph
To determine the criterion validity of the FitBit® Flex™ compared to the ActiGraph's Bluetooth® Smart wGT3X-BT wireless activity monitor, and contribute to the clinical utility of accelerometry measurement of UE movement.
Study Overview
Status
Completed
Conditions
Detailed Description
Participants will wear two different accelerometers (FitBit and Actigraph) to record normal, everyday movement.
Data from each accelerometer will be compared to determine similarity.
Study Type
Observational
Enrollment (Actual)
71
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Healthy adults
Description
Inclusion Criteria:
- Healthy adults with no upper extremity limitations
Exclusion Criteria:
- Upper extremity limitations
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Ecologic or Community
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
---|
Healthy adults
Healthy adults without any limitations in upper extremity movement or function.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Steps
Time Frame: 24 hours
|
Number of steps
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2015
Primary Completion (Actual)
May 1, 2016
Study Completion (Actual)
May 1, 2016
Study Registration Dates
First Submitted
April 11, 2017
First Submitted That Met QC Criteria
April 13, 2017
First Posted (Actual)
April 19, 2017
Study Record Updates
Last Update Posted (Actual)
April 19, 2017
Last Update Submitted That Met QC Criteria
April 13, 2017
Last Verified
April 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- FitBit vs Actigraph
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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