Viewing Study NCT01541657



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Last Modification Date: 2024-10-26 @ 10:47 AM
Study NCT ID: NCT01541657
Status: COMPLETED
Last Update Posted: 2018-01-26
First Post: 2012-02-20

Brief Title: Sensory-Targeted Ankle Rehabilitation Strategies STARS
Sponsor: Joel Thompson
Organization: University of Kentucky

Study Overview

Official Title: Sensory-Targeted Ankle Rehabilitation Strategies
Status: COMPLETED
Status Verified Date: 2018-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: STARS
Brief Summary: The purpose of this study is to determine the effect of 3 types of sensory-targeted rehabilitation interventions on subjective and objective measures of function for those with chronic ankle instability The investigators hypothesize that subjective and objective measures of function including self-reported disability balance and range of motion will improve after 2-weeks of sensory-targeted interventions
Detailed Description: The purpose of this study is to determine the effect of 3 types of sensory-targeted rehabilitation interventions on subjective and objective measures of function for those with chronic ankle instability If a potential participant is deemed eligible for participation and consents to participate heshe undergo a pretest session in which balance gait and range of motion will be assessed The participant will then be randomized into one of the 4 treatment groups and undergo the first treatment which takes approximately 5 minutes After completion of the first treatment the participant will be immediately retested on the balance gait and range of motion measures Upon completion of testing on the first day participants in the treatment groups will be asked to return for 5 more treatments over the course of 2 weeks Upon completion of the treatments each participant will be tested on their balance gait and range of motion again Then after 1 month each participant will be contacted to do a self-reported function follow-up visit in which heshe will be asked to report how stable and functional hisher ankle has been over the past month

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None