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NCT03120039 Clinical Trial

Measuring Upper Extremity Functional Movement With Accelerometry: FitBit® vs Actigraph®

Motor Activity Clinical Trial

Official title:
Measuring Upper Extremity Functional Movement With Accelerometry: FitBit vs Actigraph

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03120039
Other study ID # FitBit vs Actigraph
Secondary ID
Status Completed
Phase N/A
First received April 11, 2017
Last updated April 13, 2017
Start date May 1, 2015
Est. completion date May 1, 2016

Study information
Verified date April 2017
Source Rowe, Veronica, M.D.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 71
Est. completion date May 1, 2016
Est. primary completion date May 1, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Healthy adults with no upper extremity limitations

Exclusion Criteria:

- Upper extremity limitations

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Rowe, Veronica, M.D.

Outcome
Type Measure Description Time frame Safety issue
Primary Steps Number of steps 24 hours
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