Actively Recruiting
Effects of Rhythmic Auditory Stimulation on Range of Motion in Post- Fracture Rehabilitation of Lower Limb
Led by Riphah International University · Updated on 2026-05-12
17
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to investigate the effects of rhythmic auditory stimulation on pain levels and range of motion in children undergoing post-fracture rehabilitation of the lower limb. It seeks to determine whether incorporating rhythmic auditory cues can help reduce pain and improve joint mobility during the recovery process.
CONDITIONS
Official Title
Effects of Rhythmic Auditory Stimulation on Range of Motion in Post- Fracture Rehabilitation of Lower Limb
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age typically 5 to 18 years
- Closed lower limb fracture (tibia, fibula, femur, ankle) treated non-surgically with immobilization such as cast, splint, or brace
- Currently in rehabilitation stage, not immediate post-operative trauma care
- In sub-acute or post-casting phase where active range of motion and gait training are indicated
- Within 4 to 6 weeks post-fracture
- Able to follow instructions and participate in rhythmic auditory stimulation sessions
- Medically stable and cleared for physical therapy
You will not qualify if you...
- Involvement in acute emergency management studies
- Multiple fractures or other significant injuries
- Known hearing impairments affecting response to auditory stimulation
- Cognitive or neurological impairments affecting participation
- Pre-existing chronic pain conditions affecting pain assessments
- Recent surgeries or medical conditions contraindicating physical therapy or rhythmic auditory stimulation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CLC
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
Research Team
I
Imran Amjad, Phd
CONTACT
M
Muhammad Asif Javed, PhD*
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here