Effects Of Rehabilitation Incorporating Gait Training On Clinical Measures Associated With Chronic Ankle Instability

Chronic Ankle Instability Clinical Trial

Official title:

Effects Of Rehabilitation Incorporating Gait Training On Clinical Measures Associated With Chronic Ankle Instability

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02533037
• Other study ID #: 16992
• Status: Completed
• Phase: Phase 2/Phase 3
• First received: August 21, 2015
• Last updated: August 21, 2015
• Start date: August 2013
• Est. completion date: July 2014

Study information

• Verified date: August 2015
• Source: University of Virginia
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This is a randomized controlled trial (RCT) regarding the conservative treatment of chronic ankle instability (CAI) with an impairment based rehabilitation program. Individuals with CAI have deficits in neuromuscular control and altered gait patterns. Ankle destabilization shoes are used clinically and may improve neuromuscular control by increasing lower extremity muscle activation, which may improve gait patterns. The investigators' purpose is to determine whether a 4-week rehabilitation program that includes ankle destabilization shoes (experimental) has beneficial effects on self-reported function and ankle gait kinematics compared to traditional rehabilitation without destabilization shoes (control) in CAI patients. In addition, the investigators will compare ankle strength and balance between CAI patients and healthy individuals with no history of ankle injury prior to the 4-week rehabilitation. The investigators hypothesize the experimental group will have greater improvement in self-reported function and frontal and sagittal plane kinematics during walking compared to the control group. In addition, the investigators hypothesize that patients with CAI will have a decrease in ankle strength and balance when compared to healthy individuals. The design is a single-blinded randomized controlled trial. Forty CAI patients will complete baseline self-reported function questionnaires and walking gait trials and then be randomized into control and experimental groups. Both groups will complete 4-weeks of supervised rehabilitation with or without destabilization shoes and then repeat the questionnaires and walking trials.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: July 2014
• Est. primary completion date: July 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• CAI with a history of recurrent ankle sprains, with the first sprain occurring longer than 12 months ago. Participants will have lingering symptoms, and disability, but have not actively sought treatment for their CAI

• All participants will be physically active: Participating in some form of physical activity for at least 20 min per day, three times per week.

Exclusion Criteria:

• Neurological or vestibular disorders affecting balance

• Currently seeking medical care for CAI

• History of prior ankle surgery

• History of ankle sprain within the past 6 weeks

• History of ankle fracture

• Diabetes mellitus

• Current self-reported disability due to lower extremity pathology that may adversely affect neuromuscular function

• Lumbosacral radiculopathy

• Pregnant

• Soft tissue disorders including Marfan's syndrome and Ehlers-Dandros syndrome

Study Design

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

Related Conditions & MeSH terms

• Chronic Ankle Instability

Intervention

Other:
• Traditional Instability Tools
Participants will complete 12 sessions over 4-weeks of impairment-based rehabilitation that incorporates ankle range of motion, ankle strength, balance, and functional activity exercises. For the balance and functional activity exercises, participants will use traditional instability tools.
• Ankle Destabilization Shoes
Participants will complete 12 sessions over 4-weeks of impairment-based rehabilitation that incorporates ankle range of motion, ankle strength, balance, and functional activity exercises. For the balance and functional activity exercises, participants will use ankle destabilization shoes.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Virginia

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes from baseline in self-reported function as measured by the Foot and Ankle Ability Measure questionnaire	Scores range from 100%(no decrease in function) to 0%(complete loss of function)	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in ankle range of motion measured in degrees	Four different ankle ranges of motion will be measured using a bubble inclinometer	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in ankle maximum voluntary isometric strength	Ankle maximum voluntary isometric strength will be measured during five different ankle positions using a hand-held dynamometer.	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in balance	Static balance will be measured by participants standing on one limb on a forceplate to measure the participant's center of pressure.	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in lower extremity electromyography during ankle maximal voluntary isometric strength testing	Lower extremity electormyography during maximal isometric strength testing will be measured using surface EMG electrodes over the peroneus brevis, peroneus longus, anterior tibialis, and medial gastrocnemius muscles.	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in lower extremity electromyography during balance	Lower extremity electormyography during balance testing will be measured using surface EMG electrodes over the peroneus brevis, peroneus longus, anterior tibialis, and medial gastrocnemius muscles.	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in lower extremity kinematics during walking	Ankle, knee, and hip motion during walking measured by a 3D motion capture system	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in lower extremity kinetics during walking	Ankle, knee, and hip moments during walking measured by a 3D motion capture system	after 4-weeks of rehabilitation	No
Secondary	Changes from baseline in lower extremity surface electromyography during walking	Lower extremity electormyography during walking will be measured using surface EMG electrodes over the peroneus brevis, peroneus longus, anterior tibialis, and medial gastrocnemius muscles.	after 4-weeks of rehabilitation	No