Impact of a Targeted 8-Week Exercise Program on Pain Measures and Isokinetic Muscle Strength in Females With Patellofemoral Pain Syndrome
2 other identifiers
interventional
30
1 country
1
Brief Summary
Patellofemoral pain syndrome (PFPS) is condition characterized by anterior knee pain that predominantly affects young and physically active females. The etiology of PFPS is multifactorial, involving biomechanical, muscular, and neuromuscular factors that contribute to altered patellar tracking and increased pain sensitivity.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2025
CompletedFirst Submitted
Initial submission to the registry
May 19, 2025
CompletedFirst Posted
Study publicly available on registry
May 28, 2025
CompletedJuly 28, 2025
July 1, 2025
2 months
May 19, 2025
July 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
pain intensity
measured by Visual Analogue Scale. a score range from 0 to 10. 0 means no pain and 10 means severe pain
two times of testing (before and 8 weeks after intervention)
Study Arms (2)
group A (patients with PFPS)
OTHERpatients receive specific weight bearing program known as weight bearing exercise for better balance program
control group
NO INTERVENTIONpatient will not receive any intervention
Interventions
eight weeks of targeted weight bearing program
Eligibility Criteria
You may qualify if:
- Eligible participants will present with clinically diagnosed anterior knee pain exacerbated by activities such as stair climbing, squatting, or prolonged sitting, with a pain duration of at least three months to ensure chronicity. All participants will possess adequate intellectual and cognitive abilities to comprehend and follow exercise instructions, and they will provide informed consent prior to enrollment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Faculty of Physical Therapy, Cairo University
Giza, 12511, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof. Dr
Study Record Dates
First Submitted
May 19, 2025
First Posted
May 28, 2025
Study Start
March 2, 2025
Primary Completion
April 30, 2025
Study Completion
April 30, 2025
Last Updated
July 28, 2025
Record last verified: 2025-07