Actively Recruiting
To Evaluate the Efficiency and Results of Adding BFR to the Physical Therapy Program fo Managing Adolescents Presented With Spasmotic Flatfoot Deformities Compared to the Standard Physical Therapy Program Without BFR
Led by Assiut University · Updated on 2026-01-15
40
Participants Needed
1
Research Sites
67 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this randomized clinical trial is to evaluate the efficiency and results of adding blood flow restriction (BFR) training to the physical therapy program for managing adolescents presented with spasmotic flatfoot deformities compared to the Standard physical therapy program without blood flow restriction.
CONDITIONS
Official Title
To Evaluate the Efficiency and Results of Adding BFR to the Physical Therapy Program fo Managing Adolescents Presented With Spasmotic Flatfoot Deformities Compared to the Standard Physical Therapy Program Without BFR
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adolescents presented with idiopathic, rigid, spasmodic flatfeet.
- Age should be younger than 18 years old.
- Patients who did not respond to initial medical treatment for three weeks.
You will not qualify if you...
- Generalised tarsal arthritis.
- Neurological disorder.
- Secondary rigid flatfoot deformity.
- Patients who did not complete the follow up or evaluation protocol.
- Patients who will refuse to participate.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Assiut University Hospital, Physical Therapy Unit
Asyut, Egypt
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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