The Effect of Strain-counterstrain on Ankle Instability

NCT ID: NCT02025569

Last Updated: 2014-01-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

27 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-01-31

Study Completion Date

2009-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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).

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Other Instability, Ankle and Foot

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Experimental group

Strain counterstrain intervention

Group Type EXPERIMENTAL

Strain Counterstrain

Intervention Type OTHER

Control Group

Sham Strain Counterstrain intervention

Group Type SHAM_COMPARATOR

Sham strain counterstrain

Intervention Type OTHER

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Strain Counterstrain

Intervention Type OTHER

Sham strain counterstrain

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Long Island University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Cristiana Kahl Collins, PT, PhD

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Cristiana K Collins, PhD

Role: PRINCIPAL_INVESTIGATOR

Long Island University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Long Island University

Brooklyn, New York, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CKCollins-SCS

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Ankle Manual Therapy for Ankle Sprains
NCT00888498 SUSPENDED PHASE2/PHASE3
The Spraino Pilot Trial
NCT03311490 TERMINATED NA