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Ankle Instability Using Foot Intensive Rehabilitation (FIRE)

Primary Purpose

Ankle Injuries, Ankle Sprains

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Standard of Care Rehabilitation (SOC)
Foot Intensive Rehabilitation (FIRE)
Sponsored by
Matthew Hoch
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ankle Injuries focused on measuring chronic ankle instability, rehabilitation, injury

Eligibility Criteria

18 Years - 44 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Aged 18-44.
  2. Previous history of at least 1 ankle sprain and at least 2 episodes of "giving way" in the past 3 months.
  3. Participants must answer "yes" to at least 5 questions on the Ankle Instability Instrument.
  4. Score of 11 or higher on the Identification of Functional Ankle Instability (IdFAI).
  5. Confirmed clinical presentation of CAI by a PT, AT, or MD.

Exclusion Criteria:

  1. Sustained an ankle sprain in the previous four weeks or lower extremity neuromusculoskeletal injury other than to the ankle in the last 12 months.
  2. History of surgery to the lower extremity.
  3. Sustained a lower extremity fracture.
  4. History of neurological disease, vestibular or visual disturbance or any other pathology that would impair their sensorimotor performance.
  5. Current participation in a formal ankle joint rehabilitation program.
  6. Sustained a concussion in the last 12 months.
  7. Exhibit clinical examination characteristics of foot and ankle function which are consistent with conditions other than CAI (i.e. fracture, deformity).

Sites / Locations

  • University of KentuckyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard of Care (SOC)

Foot Intensive Rehabilitation (FIRE)

Arm Description

Participants will be randomized to receive standard of care rehabilitation (SOC) for a period of 6 weeks.The investigators will prospectively follow participants assigned to the SOC group for 24 months following completion of their assigned SOC intervention.

Participants will be randomized to receive foot intensive rehabilitation (FIRE) for a period of 6 weeks.The investigators will prospectively follow participants assigned to the FIRE group for 24 months following completion of their assigned SOC intervention.

Outcomes

Primary Outcome Measures

Number of recurrent ankle sprains
The ability of FIRE to attenuate the occurrence of ankle sprains compared to SOC rehabilitation will be determined through self-report. An ankle sprain will be operationally defined as an incident in which the rearfoot was inverted or supinated and resulted in a combination of swelling, pain, and time lost or modification of normal function for at least one day.
Frequency of episodes of the ankle giving way
The ability of FIRE to attenuate the number of episodes of the ankle giving way compared to SOC rehabilitation will be determined through self-reported occurrences per week in the past month. Episodes of giving way will be operationally defined for the subject as an incident in which the rearfoot suddenly rolled, felt weak, or lost stability; however, the individual did not sustain an ankle sprain and was able to continue with normal function.
Severity of chronic ankle instability related symptoms
The ability of FIRE to attenuate the severity of related symptoms compared to SOC rehabilitation will be determined through the Cumberland Ankle Instability Tool. The Cumberland Ankle Instability Tool is a 9-item instrument used to identify self-reported impairments associated with CAI. This instrument is scored on a 0-30 scale, where lower scores represent greater severity of CAI related symptoms.

Secondary Outcome Measures

Postural Control
The ability of FIRE to improve static and dynamic postural control compared to SOC rehabilitation will be determined. Multiple measurements will be made including: Single-limb stance on each limb with eyes open and eyes closed with use of a force plate for center of pressure measurements, Star Excursion Balance Test, forward jump single limb landing stabilization task. All measurements will be monitored while the participant wears an inertial sensor placed on the lumbar spine.
Ankle/Toe Strength
The ability of FIRE to improve strength compared to SOC rehabilitation will be determined. Strength of the muscles surrounding the ankle and the toes will be assessed through a series of assessments with a digital handheld dynamometer.
Intrinsic Foot Muscle Activation
The ability of FIRE to improve foot muscle activation compared to SOC rehabilitation will be determined. Abductor hallucis, flexor digitorum brevis, quadratus plantae, and flexor hallucis brevis functional activity ratios will be captured using diagnostic ultrasound with a 12-4 MHz linear array transducer probe and measured using Image J software.
Plantar Cutaneous Sensation
The ability of FIRE to improve plantar cutaneous sensation compared to SOC rehabilitation will be determined. Plantar cutaneous sensation will be tested using a 20-piece Semmes-Weinstein Monofilament kit which has monofilaments ranging from to 0.008g of force (1.65 level) to 300g of force (6.65 level). Light touch detection thresholds will be assessed on the plantar surface at the 1st metatarsal head.

Full Information

First Posted
July 20, 2020
Last Updated
January 10, 2023
Sponsor
Matthew Hoch
Collaborators
University of Virginia, Naval Health Research Center, Marine Corps Base Camp Pendleton
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1. Study Identification

Unique Protocol Identification Number
NCT04493645
Brief Title
Ankle Instability Using Foot Intensive Rehabilitation
Acronym
FIRE
Official Title
Optimizing Clinical Outcomes for Patients With Chronic Ankle Instability Using Foot Intensive Rehabilitation
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 28, 2021 (Actual)
Primary Completion Date
October 1, 2024 (Anticipated)
Study Completion Date
October 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Matthew Hoch
Collaborators
University of Virginia, Naval Health Research Center, Marine Corps Base Camp Pendleton

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall objective of this study is to examine the effects of a 6-week foot-intensive rehabilitation (FIRE) program on lateral ankle sprain (LAS) re-injury rates, CAI symptoms, sensorimotor function, and self-reported disability in CAI patients.
Detailed Description
Lateral ankle sprains are one of the most common injuries sustained by the general population with the greatest rates in people who are physically active or service members. Approximately 40% of lateral ankle sprain patients develop chronic ankle instability (CAI) characterized by recurrent lateral ankle sprains, repetitive sensations of ankle "giving way", residual ankle sprain symptoms, and self-reported disability. Factors related to the development and progression of CAI has been thoroughly studied. However, few interventions have been developed which have successfully created long term reductions in re-injury rates, physical function, or health-related quality of life. Recent work by our research team has uncovered several novel motor and sensory deficits in the foot in patients with CAI. Deficits in foot function may contribute to the high re-injury rates, deficits in balance and strength, and diminished health-related quality of life commonly experienced by individuals with CAI. The investigators expect the additive effect of FIRE with components of the standard of care (balance training, strength training, and range of motion) will create the synergy needed to reduce future injuries (Aim 1), enhance physical function (Aim 2), and reduce self-reported disability in CAI patients (Aim 3).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankle Injuries, Ankle Sprains
Keywords
chronic ankle instability, rehabilitation, injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The investigators will compare clinical and innovative outcome measures collected at five time points between cohorts of patients with CAI that receive a standard of care (SOC) rehabilitation program compared to an innovative foot intensive rehabilitation (FIRE) program to determine if FIRE can further reduce the rate of re-injury, improve sensorimotor function, and reduce self-reported disability during the 24 months following the intervention.
Masking
Outcomes Assessor
Masking Description
The investigators collecting the outcomes will be blinded to group allocation. Separate investigators will be used for intervention delivery and outcomes assessment.
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard of Care (SOC)
Arm Type
Active Comparator
Arm Description
Participants will be randomized to receive standard of care rehabilitation (SOC) for a period of 6 weeks.The investigators will prospectively follow participants assigned to the SOC group for 24 months following completion of their assigned SOC intervention.
Arm Title
Foot Intensive Rehabilitation (FIRE)
Arm Type
Experimental
Arm Description
Participants will be randomized to receive foot intensive rehabilitation (FIRE) for a period of 6 weeks.The investigators will prospectively follow participants assigned to the FIRE group for 24 months following completion of their assigned SOC intervention.
Intervention Type
Behavioral
Intervention Name(s)
Standard of Care Rehabilitation (SOC)
Intervention Description
6 weeks of standard of care rehabilitation will be given designed to restore ankle joint range of motion, strength, postural control, and functional movement. Each participant will be expected to complete 2 supervised sessions and 3 unsupervised at home sessions per week.
Intervention Type
Behavioral
Intervention Name(s)
Foot Intensive Rehabilitation (FIRE)
Intervention Description
6 weeks of FIRE will be given along with elements of SOC. Each participant will be expected to complete 2 supervised sessions and 3 unsupervised at home sessions per week.
Primary Outcome Measure Information:
Title
Number of recurrent ankle sprains
Description
The ability of FIRE to attenuate the occurrence of ankle sprains compared to SOC rehabilitation will be determined through self-report. An ankle sprain will be operationally defined as an incident in which the rearfoot was inverted or supinated and resulted in a combination of swelling, pain, and time lost or modification of normal function for at least one day.
Time Frame
24 months
Title
Frequency of episodes of the ankle giving way
Description
The ability of FIRE to attenuate the number of episodes of the ankle giving way compared to SOC rehabilitation will be determined through self-reported occurrences per week in the past month. Episodes of giving way will be operationally defined for the subject as an incident in which the rearfoot suddenly rolled, felt weak, or lost stability; however, the individual did not sustain an ankle sprain and was able to continue with normal function.
Time Frame
24 months
Title
Severity of chronic ankle instability related symptoms
Description
The ability of FIRE to attenuate the severity of related symptoms compared to SOC rehabilitation will be determined through the Cumberland Ankle Instability Tool. The Cumberland Ankle Instability Tool is a 9-item instrument used to identify self-reported impairments associated with CAI. This instrument is scored on a 0-30 scale, where lower scores represent greater severity of CAI related symptoms.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Postural Control
Description
The ability of FIRE to improve static and dynamic postural control compared to SOC rehabilitation will be determined. Multiple measurements will be made including: Single-limb stance on each limb with eyes open and eyes closed with use of a force plate for center of pressure measurements, Star Excursion Balance Test, forward jump single limb landing stabilization task. All measurements will be monitored while the participant wears an inertial sensor placed on the lumbar spine.
Time Frame
24 months
Title
Ankle/Toe Strength
Description
The ability of FIRE to improve strength compared to SOC rehabilitation will be determined. Strength of the muscles surrounding the ankle and the toes will be assessed through a series of assessments with a digital handheld dynamometer.
Time Frame
24 months
Title
Intrinsic Foot Muscle Activation
Description
The ability of FIRE to improve foot muscle activation compared to SOC rehabilitation will be determined. Abductor hallucis, flexor digitorum brevis, quadratus plantae, and flexor hallucis brevis functional activity ratios will be captured using diagnostic ultrasound with a 12-4 MHz linear array transducer probe and measured using Image J software.
Time Frame
24 months
Title
Plantar Cutaneous Sensation
Description
The ability of FIRE to improve plantar cutaneous sensation compared to SOC rehabilitation will be determined. Plantar cutaneous sensation will be tested using a 20-piece Semmes-Weinstein Monofilament kit which has monofilaments ranging from to 0.008g of force (1.65 level) to 300g of force (6.65 level). Light touch detection thresholds will be assessed on the plantar surface at the 1st metatarsal head.
Time Frame
24 months
Other Pre-specified Outcome Measures:
Title
Self-Reported Ankle Function
Description
The ability of FIRE to improve disability outcomes compared to SOC rehabilitation will be determined. Self-reported disability will be assessed using the Foot and Ankle Ability Measure (FAAM). Sports and activities of daily living subscale scores will be calculated.
Time Frame
24 months
Title
Self-Reported Disability
Description
The ability of FIRE to improve disability outcomes compared to SOC rehabilitation will be determined. Self-reported disability will be assessed using the Disablement in the Physically Active Scale (DPA).
Time Frame
24 months
Title
Self-Reported Fear Avoidance Beliefs
Description
The ability of FIRE to improve disability outcomes compared to SOC rehabilitation will be determined. Self-reported disability will be assessed using the Fear Avoidance Beliefs Questionnaire.
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18-44. Previous history of at least 1 ankle sprain and at least 2 episodes of "giving way" in the past 3 months. Participants must answer "yes" to at least 5 questions on the Ankle Instability Instrument. Score of 11 or higher on the Identification of Functional Ankle Instability (IdFAI). Confirmed clinical presentation of CAI by a PT, AT, or MD. Exclusion Criteria: Sustained an ankle sprain in the previous four weeks or lower extremity neuromusculoskeletal injury other than to the ankle in the last 12 months. History of surgery to the lower extremity. Sustained a lower extremity fracture. History of neurological disease, vestibular or visual disturbance or any other pathology that would impair their sensorimotor performance. Current participation in a formal ankle joint rehabilitation program. Sustained a concussion in the last 12 months. Exhibit clinical examination characteristics of foot and ankle function which are consistent with conditions other than CAI (i.e. fracture, deformity).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Douglas Long, M.S.
Phone
859-323-5438
Email
delong2@uky.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Matthew Hoch, Ph.D.
Phone
859-323-9850
Email
matt.hoch@uky.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew Hoch, Ph.D.
Organizational Affiliation
University of Kentucky
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Kentucky
City
Lexington
State/Province
Kentucky
ZIP/Postal Code
40536-0200
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Douglas Long, M.S.
Phone
859-323-5438
Email
delong2@uky.edu
First Name & Middle Initial & Last Name & Degree
Matt Hoch, Ph.D.
Phone
859-323-9850
Email
matt.hoch@uky.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Ankle Instability Using Foot Intensive Rehabilitation

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