Skip to main content
Clinical Trials/NCT02682303
NCT02682303
Completed
Not Applicable

Effect of Elastic Bandage on Measurements of Balance in Subjects With Chronic Ankle Instability: a Randomized Clinical Trial

Universidad Rey Juan Carlos1 site in 1 country28 target enrollmentMarch 2016
ConditionsAnkle Sprain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ankle Sprain
Sponsor
Universidad Rey Juan Carlos
Enrollment
28
Locations
1
Primary Endpoint
Balance using a computerized dynamic posturography test: the sensory organization test
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Purpose: To report the immediate and prolonged (one week) effects of elastic bandage on balance control in subjects with chronic ankle instability.

Material and methods: Twenty-eight individuals successfully completed the study protocol, of whom 14 were randomly assigned to the elastic bandage group (7 men, 7 women) and 14 were assigned to the non-standardized tape group ( 9 men, 5 women). To objectively measure postural sway we used computerized dynamic posturography with Sensory Organization Test and Unilateral Stance test. We analyzed the following Sensory Organization Test parameters: the composite Sensory Organization Test score, the composite Sensory Organization Test strategy and the Sensory Organization Test condition 2 and its strategy. In addition, we studied the centre of gravity sway velocity with open eyes and close eyes during the US test.

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
August 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Josue Fernandez Carnero

PhD

Universidad Rey Juan Carlos

Eligibility Criteria

Inclusion Criteria

  • Subjects with Chronic Ankle Instability

Exclusion Criteria

  • Neurologic disease Vestibular disease

Outcomes

Primary Outcomes

Balance using a computerized dynamic posturography test: the sensory organization test

Time Frame: 7 days

The CDP device employed in this study was Smart Equitest® version 8.2 (NeuroCom International Inc., Clackamas, OR, USA). Posturography analysis was conducted using the SOT. This test assesses postural control through the use of external stimuli on the visual and proprioceptive system. Participants were instructed to stand on the force-plate facing the visual surround. A safety harness was fixed to prevent injury from falls. Their bare feet position on force-plates was adjusted according to the height of the patient, as marked on the equipment. Subjects had to maintain their COG stable in 3 consecutive series of 20s duration for each of the 6 conditions in the test.

Study Sites (1)

Loading locations...

Similar Trials