NCT05585385

Brief Summary

The goal of this clinical trial is to investigate the effect of backward walking versus balance training in patients with chronic ankle instability. The main question it aims to answer is: Is there a difference between the effect of balance training and BW training on balance, ankle proprioception, risk of fall, and functional limitations in CAI patients?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 14, 2022

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 18, 2022

Completed
15 days until next milestone

Study Start

First participant enrolled

November 2, 2022

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2023

Completed
24 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 25, 2023

Completed
Last Updated

July 18, 2023

Status Verified

July 1, 2023

Enrollment Period

7 months

First QC Date

October 14, 2022

Last Update Submit

July 16, 2023

Conditions

Outcome Measures

Primary Outcomes (3)

  • Dynamic Balance Assessment

    Dynamic balance is assessed by the Biodex stability system which has a high level of accuracy in determining dynamic equilibrium for postural control testing. It establishes three numeric stability indexes: Overall Stability Index (OSI), Anterior/Posterior Stability Index (APSI), and Medial/Lateral Stability Index (MLSI), to assess the body's deviation from its gravity center. The OSI indicates the overall score in all directions, while the APSI and MLSI represent the sagittal and frontal planes, respectively. The higher the stability, the lower the ranking.

    up to 6 weeks

  • Active repositioning accuracy of ankle joint

    Ankle proprioception will be assessed by a digital goniometer. The starting position for ankle joint testing is 90 degree. The maximum ankle planter flexion for each subject will be measured, and half this max. range will be selected as the target position. Subjects will be asked to remain in that position for 10 seconds. The subject with closed eyes actively moves the ankle from starting position (90 degrees) to the targeted plantar-flexion angle with constant speed during the test (they were asked to return to the initial position and progressively move towards the target degree). This process would be repeated 3 times and the average error in active repositioning of the targeted angle would be taken.

    up to 6 weeks

  • Functional limitations

    Functional disability will be assessed by the Foot and Ankle Disability Index (FAID).This index is a 34-item questionnaire divided into subscales, FADI and FADI sport. FADI contains 4 pain related items and 22 activity related items, while the FADI sport contains 8 activity related items. Each question can be scored on a 5- point Likert scale (from 0 to four). FADI and FADI sport are scored separately. FADI has total score of 104 points and FADI Sport 32 points. Both are transformed into percentage.

    up to 6 weeks

Study Arms (3)

Backward Walking Training

EXPERIMENTAL

The patients will receive BW training in addition to the traditional physical therapy program for 6 weeks.

Device: Backward Walking Training

Balance Training

EXPERIMENTAL

The patients will receive balance training on the Biodex balance system in addition to the traditional physical therapy program for 6 weeks.

Device: Balance Training

conventional treatment

ACTIVE COMPARATOR

The patients will receive the traditional physical therapy program only for 6 weeks.

Other: Conventional treatment

Interventions

The subjects in this group will receive BW training program on an electric treadmill. The subject will be asked to walk, arms beside, in a backward manner on a level treadmill, zero inclination, with a warming up and cooling down period (5 minutes for each period). The subject walks at his self-selected and comfortable walking speed. A warm-up and cool-down period, in form of light jogging on a treadmill, will be done at speed of 1-2 m/sec. The total training is 30 minutes, three times a week for six consecutive weeks.

Backward Walking Training

Subjects in this group will receive balance training on Biodex Balance System for 3 sessions/ week, over 6 weeks period. Each subject will be instructed to stand with both legs on the "locked" platform. The researcher advances the platform to an unstable state while instructing the subject to focus on the visual feedback screen. Arms are free at the side of the body and not grasping handrails. After selecting the stability training program (dynamic balance training), Stability levels are changed depending on the subject's ability to maintain balance, and subjects are instructed to maintain their Center of Pressure (COP) in the smallest concentric rings (balance zones) of the Biodex Balance System monitor, named A zone. The stability level of the platform is set at level plate stability 8 (the most stable) for the first two sessions. After that, the plate stability is decreased by one level every two sessions to increase the difficulty in training.

Balance Training

Patients in this group will receive the traditional physical therapy program only for 3 sessions/ week, over 6 weeks period. The traditional physical therapy program is (evertors strengthening, short foot ex, heel raise ex, and calf stretch).

conventional treatment

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • All subjects will complete a questionnaire by self-report (Cumberland Ankle Instability Tool (CAIT) to be characterized as having Functional Ankle Instability (FAI) ; All subjects' scores on CAIT will be less than 23 to be severely identified with FAI. Subjects will satisfy the following criteria:
  • Having FAI that persists after the initial lateral ankle sprain and complaining of residual symptoms (repeated episodes of giving way or feeling of ankle joint instability) and suffering of repeating injury.
  • Having mechanical ankle instability on one ankle joint (will be identified by manual testing as talar tilt and anterior drawer test of the ankle to determine the integrity of ankle ligaments).
  • Their age ranges from 18 to 35 years.
  • Subjects with body mass index less than 30 kg/m2.
  • Not undergoing any formal or informal rehabilitation of the unstable ankle.

You may not qualify if:

  • Ankle joint swelling or any rheumatological disorders in both legs.
  • Ankle surgery in either leg.
  • Gross limitation in ankle range of motion in both legs.
  • Any joint disease or bony fracture in the lower extremity.
  • History of neurological disorder affecting the upper or lower extremities, vestibular dysfunction, or balance disorder.
  • Receiving formal or informal rehabilitation of their unstable ankle for 3 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Physical Therapy, Cairo University

Giza, Egypt

Location

Study Officials

  • Neveen A. Abdel Raoof, PhD

    Cairo University

    STUDY CHAIR
  • Ghada A. Abd Allah, PhD

    Cairo University

    STUDY DIRECTOR
  • Rania R. Mohamed, PhD

    Cairo University

    STUDY DIRECTOR
  • Amr A. Azzam, PhD

    National Institute of Neuromotor System

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
random generator
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Backward Walking Training and Balance Training
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant lecturer

Study Record Dates

First Submitted

October 14, 2022

First Posted

October 18, 2022

Study Start

November 2, 2022

Primary Completion

June 1, 2023

Study Completion

June 25, 2023

Last Updated

July 18, 2023

Record last verified: 2023-07

Locations