The Effect of a Treatment Protocol Focused on Neuromuscular Control Exercises on Pain and Function in a Subgroup of Individuals With Patellofemoral Pain
1 other identifier
interventional
20
1 country
1
Brief Summary
Patellofemoral Pain (PFP) is one of the most common causes of knee pain and is significantly present in recreational athletes who have previously been categorized as being in a subgroup of PFP. Understanding which intervention is most appropriate for this subgroup could give us important information about subgroup-based treatments, which are not yet described in the literature. Therefore, the aim of this study is to analyze the effect of two exercise interventions in a PFP subgroup: one focusing on neuromuscular control exercises and the other focusing on muscle strengthening.This study will recruit 10 individuals to each exercise group, and will assess pain, function, muscle activity and joint kinematics pre and post intervention. Mixed Model ANOVA tests will be used to determine the responses to the two interventions between the two groups over a 6-week treatment time.
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 May 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
First Submitted
Initial submission to the registry
March 10, 2025
CompletedFirst Posted
Study publicly available on registry
March 25, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2025
CompletedMarch 25, 2025
March 1, 2025
3 months
March 10, 2025
March 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Pain at rest
Numerical Pain Rating Scale (NPRS)
From enrollment to the end of treatment at 6 weeks
Pain during activity
Numerical Pain Rating Scale (NPRS)
From enrollment to the end of treatment at 6 weeks
Function
Knee injury and Osteoarthritis Outcome Score - KOOS
From enrollment to the end of treatment at 6 weeks
Secondary Outcomes (3)
Kinematic data - hip, knee and ankle angles
From enrollment to the end of treatment at 6 weeks
Kinetic data - hip, knee, and ankle moments and ground reaction forces
From enrollment to the end of treatment at 6 weeks
Muscular activity
From enrollment to the end of treatment at 6 weeks
Study Arms (2)
Neuromuscular control exercises
EXPERIMENTALMuscle strengthening
ACTIVE COMPARATORInterventions
Eligibility Criteria
You may qualify if:
- Anterior or retropatellar pain reported on at least two of the following activities: prolonged sitting, ascending or descending stairs, running, kneeling and hopping/jumping.
- At least two of the three following clinical examination findings:
- Pain during resisted isometric quadriceps contraction
- Pain with palpation of the posterior borders of the patella
- Pain during squatting Classified as a subgroup of PFP.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Sport of University of Porto
Porto, 4200-450, Portugal
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
João Paulo Vilas-Boas, Full professor
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Patients will be blinded to group allocation, ensuring that they will not know which exercises will be performed by the other group, and thus the interventions will be administered separately to members of each treatment group.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD candidate
Study Record Dates
First Submitted
March 10, 2025
First Posted
March 25, 2025
Study Start
May 1, 2025
Primary Completion
August 1, 2025
Study Completion
August 1, 2025
Last Updated
March 25, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share