Actively Recruiting
Comparative Effects of Perturbation and Functional Stabilization Training on Pain, Balance and Performance in Athletes With Patellofemoral Pain Syndrome
Led by Riphah International University · Updated on 2024-07-19
26
Participants Needed
1
Research Sites
5 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The trial investigates the comparative effects of perturbation training and functional stabilization training on pain, balance, and performance in athletes with patellofemoral pain syndrome (PFPS). PFPS is a common cause of anterior knee pain caused by muscle imbalances around the knee cap, affecting young athletes aged 15 to 30. The study focuses on how these training programs impact knee pain, muscle control, balance, and athletic performance in this group. Participants are divided into two groups: one will receive functional stabilization exercises combined with traditional treatment, while the other will undergo perturbation training. The functional stabilization group will perform exercises such as lateral and ventral bridges, hip abduction and rotation, pelvic drops, single-leg deadlifts and squats, and knee flexion and extension over an 8-week period. The perturbation group will engage in balance activities like foam balance, tilt board, and roller board exercises. Both groups will begin with a 30-minute education session and undergo pre- and post-intervention assessments. During the study, participants will be evaluated using multiple tools including a numerical pain rating scale, horizontal and vertical jump tests, 40-yard sprint test, lower extremity functional scale, and star excursion balance test over 10 months. Data will be analyzed to assess changes in pain, balance, and performance. The study uses randomized allocation and single masking to compare the two training methods and monitor their effects on athletes with PFPS.
CONDITIONS
Brief Title
Comparative Effects of Perturbation and Functional Stabilization Training on Patellofemoral Pain Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Anterior knee pain
- Age between 15 to 30 years
- Knee pain rated between 3 and 10 on the numerical pain rating scale
You will not qualify if you...
- Patellar fracture
- Intra-articular pathology such as ligamental or meniscal injury of the knee
- Previous knee surgery
- Fracture of hip, knee, shin bone, or foot
- Vestibular and visual disorders
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants receive either functional stabilization training or perturbation training to manage patellofemoral pain syndrome. Training includes exercises such as bridges, hip abduction, single-leg squats, and balance activities.
Weekly visits for up to 8 weeks
Duration - Up to 10 months from start
Participants undergo assessments of pain, balance, and performance after the intervention to evaluate treatment effects.
1 to 2 follow-up visits
Trial Site Locations
Total: 1 location
1
Pakistan sports board
Lahore, Punjab Province, Pakistan, 54660
Actively Recruiting
Research Team
A
AISHA SIDDIQA, MS-DPT
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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