- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07576816
Effects of Hip-Based Versus Knee-Based Exercises on Medial Longitudinal Arch, Dynamic Balance, and Muscle Strength in Flexible Flatfoot
May 4, 2026 updated by: Dr Izza Ayub; PT, University of Faisalabad
This study aims to compare the effects of hip-based and knee-based exercise interventions on medial longitudinal arch height, dynamic balance, and lower limb muscle strength in individuals with flexible flat feet.
Participants will be randomly assigned to two groups: one receiving hip-focused strengthening and stretching exercises, and the other receiving knee-focused exercises, while both groups will perform a common set of foot intrinsic exercises.
The intervention will be conducted over 6 weeks.
Outcomes will be measured pre- and post- intervention and in the middle of intervention to determine which approach is more effective in improving foot stability and functional performance.
Study Overview
Status
Recruiting
Conditions
Study Type
Interventional
Enrollment (Estimated)
46
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Dr Izza aYUB; pt Assistant Professor
- Phone Number: 0330 1980690
- Email: drizzaayub@gmail.com
Study Locations
-
-
Punjab Province
-
Faisalābad, Punjab Province, Pakistan
- Recruiting
- Madinah Teaching Hospital
-
Contact:
- Dr Izza aYUB; pt Assistant Professor
- Phone Number: 0330 1980690
- Email: drizzaayub@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Give verbal or written consent to enter the study.
- People without any pain and in the age group of about 25-40 years.
- People in the category of normal to obese BMI.
- People whose value of navicular drop above 10mm.
Exclusion Criteria:
- People having any surgical procedure on the lower limb.
- People using any kind of orthosis.
- If the difference between the length of both legs is more than 1.1cm.
- People having any disease like diabetes, rheumatoid arthritis, plantar fasciitis or sciatica.
- People having any injury within 6 months.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A: Hip-based Exercise with hot pack and intrinsic foot strengthening exercises
|
Baseline: Hot pack will be applied to the calf muscle for 5-10 minutes.
Then the calf muscles will be stretched with 5 repetitions.
Treatment: Clamshell exercises with 4 progressions with 5-10 repetitions and iliopsoas stretching with 3 repetitions per session.
|
|
Active Comparator: Group B: Knee-based exercises with a hot pack and intrinsic foot strengthening exercises
|
Baseline: Hot pack will be applied to the calf muscle for 5-10 minutes.
Then the calf muscles will be stretched with 5 repetitions.
Treatment: Knee isometrics with 5-1o repetitions along with hamstring stretching 3 repetitions per session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lower extremity muscle strength
Time Frame: 6 weeks
|
Digital handheld dynamometer will be used to evaluate improvement in muscular performance associated with each intervention.
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Medial longitudinal arch height and dynamic balance.
Time Frame: 6 weeks
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 30, 2026
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
June 30, 2026
Study Registration Dates
First Submitted
May 4, 2026
First Submitted That Met QC Criteria
May 4, 2026
First Posted (Actual)
May 8, 2026
Study Record Updates
Last Update Posted (Actual)
May 8, 2026
Last Update Submitted That Met QC Criteria
May 4, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Talipes
- Musculoskeletal Diseases
- Musculoskeletal Abnormalities
- Congenital Abnormalities
- Lower Extremity Deformities, Congenital
- Limb Deformities, Congenital
- Foot Deformities
- Foot Deformities, Acquired
- Foot Deformities, Congenital
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Flatfoot
Other Study ID Numbers
- TUF/EIRB/185/26
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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