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External Versus Internal Feedback in Patients With Chronic Ankle Instability

External Versus Internal Feedback on Biomechanics and Self-reported Function in Patients With Chronic Ankle Instability

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04131842
Enrollment
48
Registered
2019-10-18
Start date
2020-02-18
Completion date
2024-07-01
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankle Injuries, Ankle Inversion Sprain

Brief summary

Although altered biomechanics has been well documented as an impairment associated with chronic ankle instability (CAI), effective interventions targeting biomechanics with long-term outcomes measuring patient-reported outcomes (PROs) are absent. Evidence suggests that external focus of attention (ExFOCUS), internal focus of attention (InFOCUS) feedback, and auditory feedback during movement training can alter biomechanics in other patient populations, with ExFOCUS and auditory enhancing retention of learned biomechanics. Therefore, this randomized controlled trial will determine if a 4-week (12 session) impairment-based rehabilitation program that includes feedback (ExFOCUS or InFOCUS or Auditory) can (1) decrease ankle inversion kinematics and lateral plantar pressure during walking and (2) improve self-reported function.

Interventions

OTHERExternal focus of attention visual feedback

Patients will receive external focus of attention visual feedback during the impairment-based rehabilitation program.

OTHERExternal focus of attention auditory feedback

Patients will receive external focus of attention auditory feedback during the impairment-based rehabilitation program.

OTHERInternal focus of attention video feedback

Patients will receive internal focus of attention visual feedback during the impairment-based rehabilitation program.

Patients will receive no feedback during the impairment-based rehabilitation program.

Sponsors

University of North Carolina, Charlotte
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Characterized as having chronic ankle instability (CAI) by reporting 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 ankle surgery * History of ankle sprain within the past 6 weeks * History of other musculoskeletal injuries within the past 6 weeks * Current/previous self-reported disability due to lower extremity pathology that may adversely affect neuromuscular function

Design outcomes

Primary

MeasureTime frameDescription
Changes from baseline in lower extremity kinematics and kinetics during walkingImmediate post-intervention, 1-month post-intervention, 3-months post-interventionAnkle, knee, and hip motion and moments during walking measured by a 3D motion capture system and in shoe plantar pressure system
Changes from baseline in self-reported ankle functionImmediate post-intervention, 1-month post-intervention, 3-months post-interventionChanges from baseline in self-reported function as measured by the Foot and Ankle Ability Measure (FAAM) Activities of Daily Living and Sport questionnaire. Scores range from 100% (no decrease in function) to 0% (complete loss of function).

Secondary

MeasureTime frameDescription
Changes from baseline in ankle range of motion measured in degreesImmediate post-intervention, 1-month post-intervention, 3-months post-interventionFour different ankle ranges of motion will be measured
Changes from baseline in ankle maximum voluntary isometric strengthImmediate post-intervention, 1-month post-intervention, 3-months post-interventionAnkle maximum voluntary isometric strength will be measured during four different ankle positions using a hand-held dynamometer.
Changes from baseline in static and dynamic balanceImmediate post-intervention, 1-month post-intervention, 3-months post-interventionStatic balance will be measured via a force plate and dynamic balance will be measured using the Star Excursion Balance Test

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026