Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05403944 · ClinicalTrials.gov registry record · NA
Strength or Power Training for Patellofemoral Pain
A NA study of Patellofemoral Pain, sponsored by University of Connecticut.
- Active
- Registry status
- NA
- Development phase
- 88
- Enrollment target
- 3
- Study locations
NCT05403944: Active NA study of Patellofemoral Pain, sponsored by University of Connecticut.
NCT05403944 is a NA study of Patellofemoral Pain that is active but no longer recruiting, run by University of Connecticut. The registered enrollment target is 88 participants, below the 152-participant average among 5 other Patellofemoral Pain trials with a reported enrollment target (42% lower). The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05403944, a NA study of Patellofemoral Pain, is active but no longer recruiting, sponsored by University of Connecticut.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 88 participants
- Enrollment target
- 3
- Study locations
Study Summary
The objective of this study is to compare a novel 6-week strength training rehabilitation incorporating power exercises (STRIPE) program to a standard of care (SOC) program on short-term and long-term pain, subjective function, patellofemoral pain recurrence rates, and secondary outcomes (hip abduction and extension rate of torque development and single-leg squat kinematics). We hypothesize that participants with patellofemoral pain who complete the STRIPE program will have 1) decreased pain, 2) improved subjective function, 3) reduced patellofemoral pain recurrence rates, 4a) improved hip abduction/extension rate of torque development, and 4b) decreased hip adduction and pelvic drop during a single leg squat compared to participants who complete a SOC rehabilitation program.
Primary Outcome
Data are presented as knee pain, assessed on the visual analog scale in centimeters, resulting in a score of 0-10, with 0 representing no pain and 10 being worst pain imaginable. Group means and standard deviations will be reported.
Conditions Studied
Interventions
- BEHAVIORAL Standard of Care Rehabilitation (SOC)
- BEHAVIORAL Strength Training Rehabilitation Incorporating Power Exercises (STRIPE)
Study Locations (3)
Connecticut
- University of Connecticut - Storrs
Florida
- University of Central Florida - Orlando
Ohio
- University of Toledo - Toledo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2022-10-13 |
| Est. Completion | 2027-09 |
| Phase | NA |
What the registry record for NCT05403944 still lists
NCT05403944 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 88 participants, a relatively small participant target, below the 152-participant average among 5 other Patellofemoral Pain trials with a reported enrollment target (42% lower).
The record links to 1 condition, with Patellofemoral Pain appearing as the primary indexed condition, and to 2 interventions - of which Standard of Care Rehabilitation (SOC) is the first listed.
NCT05403944 reports a single indexed study location in Connecticut, Florida, Ohio.
Frequently Asked Questions
What is clinical trial NCT05403944 about?
NCT05403944 is a clinical study titled "Strength or Power Training for Patellofemoral Pain". The objective of this study is to compare a novel 6-week strength training rehabilitation incorporating power exercises (STRIPE) program to a standard of care (SOC) program on short-term and long-term pain, subjective function, patellofemoral pain recurrence rates, and secondary outcomes (hip abduct...
What is the current status of trial NCT05403944?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 88 participants. The study started on 2022-10-13. Estimated completion is 2027-09.
What conditions does trial NCT05403944 study?
This clinical trial studies the following conditions: Patellofemoral Pain.
What interventions are being tested in trial NCT05403944?
The interventions under investigation include: Standard of Care Rehabilitation (SOC) (BEHAVIORAL), Strength Training Rehabilitation Incorporating Power Exercises (STRIPE) (BEHAVIORAL).
Who is sponsoring clinical trial NCT05403944?
This trial is sponsored by University of Connecticut, which has 107 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05403944 being conducted?
This trial has 3 study locations across Connecticut, Florida, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Patellofemoral Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Mindful Miles Pilot Feasibility Study
RECRUITING · NA
-
Emovi 3D Knee Assessment Device Intervention for Operational Readiness
RECRUITING · NA
-
Evaluating the Effectiveness of Clinical Practice Guideline Adherence for Patellofemoral Pain
RECRUITING · NA
-
Limited Ankle Dorsiflexion and Effect on Single Limb Squats in Individuals With Patellofemoral Pain
RECRUITING · NA
-
Bilateral Knee Pain and Dry Needling
ACTIVE NOT RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT03843463 · 88 participants · Phase 2
Escitalopram and Language Intervention for Subacute Aphasia
- NCT04066348 · 88 participants · Phase 2
TNF-α Treatment of Blast-Induced Tinnitus
- NCT04331704 · 88 participants · Phase 4
ANCHORS Alcohol & Sexual Health Study: UH3 Project
- NCT04536103 · 88 participants
Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI