- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07671170
Comparative Effect of Combined Strength, Core and Balance Training on Kinesiophobia, Ankle Instability, Functional Outcomes, and Performance in Table Tennis Players With Functional Ankle Instability
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ahmad Zia, MS-PT Sports
- Phone Number: +92 340 9270376
- Email: khanxia961@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male/female table tennis players aged 15-30 years
- Experienced at least one ankle sprain with swelling/pain that interrupted training for >1 day within the last 6 months
- Reported sensation of instability of the ankle
- Scored ≤25 points on the Cumberland Ankle Instability Tool (CAIT), indicating functional ankle instability
Exclusion Criteria:
- History of ankle fracture or surgery
- Any fracture of lower limb history
- Any neurological or vestibular disorders
- Other injuries of lower limb affecting performance
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental: Combined Strength and Balance Training
Participants will receive a 6-week combined strength and balance training program (3 sessions/week, 40-45 min). Strength Component: Theraband Dorsiflexion (3×12), Theraband Eversion (3×12), Heel Raises progressing to single-leg (3×12), Forward Lunges (3×10 each leg). Balance Component: Single-Leg Stance Eyes Open→Closed (3×30 sec), Wobble Board Standing (3×30 sec), Y-Balance Reach (3 trials each direction). Weekly progression: Week 1-2 basic stable surface exercises, Week 3-4 increased repetitions, Week 5-6 single-leg variations introduced. |
A structured 6-week exercise program combining ankle strengthening exercises (Theraband resistance training, heel raises, lunges) with dynamic balance training (single-leg stance, wobble board, Y-balance drills).
Sessions last 40-45 minutes and are conducted 3 times per week.
Warm-up: 5-7 min light jogging/dynamic mobility.
Main Training: 30 min combined strength and balance work.
Cool-down: 5 min static stretching.
|
|
Active Comparator: Control Group: Balance and Core Training
Participants will receive a 6-week balance and core training program (3 sessions/week, 40-45 min). Balance Component: Single-Leg Stance Firm→Foam (3×30 sec), Tandem Walking (3×10 m), Y-Balance Drill (3 trials each direction). Core Component: Plank Hold (3×20 sec), Side Plank each side (3×15 sec), Dead Bug Exercise (3×10 reps). Weekly progression: Week 1-2 basic level, Week 3-4 increased repetitions, Week 5-6 maintained progression. |
A structured 6-week program combining balance training (single-leg stance on firm and foam surfaces, tandem walking, Y-balance drills) with core stabilization exercises (plank, side plank, dead bug).
Sessions last 40-45 minutes, 3 times per week with the same warm-up and cool-down structure as the experimental group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Kinesiophobia - Tampa Scale for Kinesiophobia (TSK-17)
Time Frame: Baseline (Week 0) and Post-intervention (Week 6)
|
17-item self-report questionnaire measuring fear of movement and re-injury.
Good internal consistency (Cronbach's α = 0.70-0.86)
and test-retest reliability (ICC = 0.72-0.90).
Reduced scores indicate decreased kinesiophobia.
|
Baseline (Week 0) and Post-intervention (Week 6)
|
|
Ankle Instability - Cumberland Ankle Instability Tool (CAIT)
Time Frame: Baseline (Week 0) and Post-intervention (Week 6)
|
Validated questionnaire assessing functional ankle instability severity.
Excellent test-retest reliability (ICC = 0.96) and internal consistency (Cronbach's α = 0.83).
Increased post-intervention scores indicate improved perceived ankle stability
|
Baseline (Week 0) and Post-intervention (Week 6)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Ability - Foot and Ankle Ability Measure (FAAM)
Time Frame: Baseline (Week 0) and Post-intervention (Week 6)
|
Self-reported tool assessing functional limitations in foot and ankle disorders.
Excellent internal consistency (α = 0.89-0.98)
and reliability (ICC = 0.84-0.92)
for ADL and Sports subscales.
Increased scores indicate improved functional ability
|
Baseline (Week 0) and Post-intervention (Week 6)
|
|
Dynamic Balance - Y Balance Test (YBT)
Time Frame: Baseline (Week 0) and Post-intervention (Week 6)
|
Measures dynamic balance and lower limb neuromuscular control.
Excellent test-retest reliability (ICC = 0.85-0.91).
Reach distances normalized to limb length.
Increased post-intervention reach distance indicates improved ankle stability.
|
Baseline (Week 0) and Post-intervention (Week 6)
|
|
Functional Performance - Single-Leg Hop Test
Time Frame: Baseline (Week 0) and Post-intervention (Week 6)
|
Reliable measure of lower limb strength, dynamic stability, and functional performance (ICC = 0.85-0.95).
Increased hop distance and improved landing control indicate enhanced neuromuscular function.
|
Baseline (Week 0) and Post-intervention (Week 6)
|
|
Agility and Performance - T-Test and Illinois Agility Test
Time Frame: Baseline (Week 0) and Post-intervention (Week 6)
|
Valid and reliable measures of agility and change-of-direction speed.
T-Test (ICC = 0.90-0.98),
Illinois Agility Test (ICC = 0.88-0.96).
Reduced completion time indicates improved dynamic stability and neuromuscular control.
|
Baseline (Week 0) and Post-intervention (Week 6)
|
Collaborators and Investigators
Investigators
- Principal Investigator: Hafsah Gul Khattak, DPT, MSNMPT, Ibadat International University, Islamabad (Iiui)
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IIUI/RERC/ADT/2026/05/261
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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