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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02025569
Other study ID # CKCollins-SCS
Secondary ID
Status Terminated
Phase N/A
First received December 24, 2013
Last updated December 30, 2013
Start date January 2008
Est. completion date July 2009

Study information

Verified date December 2013
Source Long Island University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study seeks to determine the effectiveness of Strain Counterstrain in the treatment of chronic ankle instability.


Description:

This study aimed to determine the effect of Strain Counterstrain (SCS) on dynamic balance and subjective sense of instability in individuals with chronic ankle instability (CAI). Although many studies have been published on CAI, the cause for this common clinical dysfunction remains inconclusive. No studies have assessed the effectiveness of SCS on CAI. Baseline information on all participants includes a demographic questionnaire, the Star Excursion Balance Test (SEBT), and the Foot and Ankle Ability Measure (FAAM). Participants were randomized into the SCS intervention group or the sham SCS control group. All participants received an intervention (as assigned) once a week for four weeks in addition to performing a prescribed home exercise program. At week four all participants repeated the outcome measures and completed a Global Rating of Change (GROC) form. The primary aim was examined with a 2-way analysis of variance (ANOVA).


Recruitment information / eligibility

Status Terminated
Enrollment 27
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- history of at least 1 ankle sprain, with pain and/or limping for more than 1 day, at least 3 months earlier

- 3 of more episodes of ankle giving way in the last 12 months

- chronic instability attributed to the original sprain injury

- age between 18-55

Exclusion Criteria:

- history of fracture or surgery in the affected ankle

- any other lower extremity musculoskeletal injury on the side of the involved ankle

- vestibular dysfunction or disorder

- history of balance dysfunction

- history of stroke or any other neurological pathology or disease

- history of ACL injury

- current participation in physical therapy or rehabilitation for the ankle injury

- evidence of CNS dysfunction

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Other Instability, Ankle and Foot

Intervention

Other:
Strain Counterstrain

Sham strain counterstrain


Locations

Country Name City State
United States Long Island University Brooklyn New York

Sponsors (1)

Lead Sponsor Collaborator
Long Island University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Star Excursion Balance Test A measure assessing dynamic standing balance as the individual stands on one leg and reaches, with the other leg, in eight different directions. The distances reached with the non-stance leg are measured. baseline No
Primary Star Excursion Balance Test A measure assessing dynamic standing balance as the individual stands on one leg and reaches, with the other leg, in eight different directions. The distances reached with the non-stance leg are measured. 4 weeks No
Secondary Foot and Ankle Ability Measure This measures assesses ankle function skills subjectively via a questionnaire baseline No
Secondary Foot and Ankle Ability Measure This measures assesses ankle function skills subjectively via a questionnaire 4 weeks No
See also
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