- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02931916
Evaluation of Reliability and Validity of a Smart-phone Postural Control Assessment Application
October 24, 2018 updated by: Wen-Hsu Sung, National Yang Ming University
Evaluation of Reliability and Validity of a Smart-phone Application Designed for Chronic Ankle Instability Subjects' Postural Control Assessment
The purpose of this study is to evaluate the reliability and validity of smart-phone based system in postural control ability assessment on subjects with chronic ankle instability.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
138
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Taipei, Taiwan
- Yang Ming university
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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
20 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
chronic ankle instability group
Description
Inclusion Criteria:
- clinical diagnosis of ankle functional instability
Exclusion Criteria:
- any other condition would affect postural control performance
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
Cohorts and Interventions
Group / Cohort |
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healthy group
recruited for evaluation of system reliability
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Chronic Ankle Instability group
recruited for evaluation of system validity
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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physiological parameter: acceleration data from built-in sensor with unit: m/s^2
Time Frame: 40 seconds
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Using the built-in sensor to record the acceleration data during each seconds trial. Both x, y and z axialis will be recorded |
40 seconds
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physiological parameter: orientation data from built-in sensor with unit: degree
Time Frame: 40 seconds
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Using the built-in sensor to record the acceleration data during each seconds trials. Both x, y and z axialis will be recorded |
40 seconds
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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
November 1, 2016
Primary Completion (Actual)
March 30, 2018
Study Completion (Actual)
August 31, 2018
Study Registration Dates
First Submitted
September 29, 2016
First Submitted That Met QC Criteria
October 11, 2016
First Posted (Estimate)
October 13, 2016
Study Record Updates
Last Update Posted (Actual)
October 25, 2018
Last Update Submitted That Met QC Criteria
October 24, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 2016CAIAppR&V
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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