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Clinical Trial NCT07287267 for Patello Femoral Syndrome is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
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Exploring the Relationship Between Range of Motion in Knee Rehabilitation Exercises and Pain in Patellofemoral Pain Syndrome 15 Observational Exercise-Based
Clinical Trial NCT07287267 is an observational study for Patello Femoral Syndrome that is recruiting. It started on 1 December 2024 with plans to enroll 15 participants. Led by Ted Gunhamn, it is expected to complete by 1 April 2026. The latest data from ClinicalTrials.gov was last updated on 17 December 2025.
Brief Summary
This study aims to investigate the relationship between knee joint range of motion and pain in patients with patellofemoral pain syndrome (PFPS). In a cross-sectional observational design, PFPS patients will perform trials involving progressively increased knee joint range of motion in three closed-chain exercises: squat, single-leg squat, and split squat. During each trial, participants will report pain levels on a ...Show More
Official Title
Exploring the Relationship Between Range of Motion in Knee Rehabilitation Exercises and Pain in Patellofemoral Pain Syndrome
Conditions
Patello Femoral SyndromeOther Study IDs
- 2024-01422-01
NCT ID Number
Start Date (Actual)
2024-12-01
Last Update Posted
2025-12-17
Completion Date (Estimated)
2026-04-01
Enrollment (Estimated)
15
Study Type
Observational
Status
Recruiting
Keywords
Patellofemoral pain syndrome
Range of motion
patellofemoral pain
Range of motion
patellofemoral pain
Arms / Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
Patellofemoral Pain Syndrome Patients diagnosed with patellofemoral pain syndrome by health care provider. | Exercise Exercise with progressively increased range of motion. |
Primary Outcome Measures
Secondary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Pain (VAS) | Pain measured 0-10 visual analog scale (VAS) reported during each trial of progressively increased range of motion during a single session. | Day 1 (Cross sectional single session. Outcomes will be collected during one single session for each participant.) |
Range of motion | Degrees of knee flexion measured during each trial in one single session. | Day 1 (Cross sectional single session. Outcomes will be collected during one single session for each participant.) |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Force | Force (N) (peak value) reported during the different trials in one session. Measured by force plates. | Day 1 (Cross sectional single session. Outcomes will be collected during one single session for each participant.) |
Tegner Activity Scale (TAS) | The Tegner Activity Scale (TAS) will be used to assess the physical activity levels of the participants. Scale from 1-10 where 10 is highest possible physical activity and 1 is sedentary. | Baseline (Administered at the beginning of the study) |
Participation Assistant
Eligibility Criteria
Eligible Ages
Child, Adult
Minimum Age
15 Years
Eligible Sexes
All
- Patients diagnosed with PFP in only one knee by a licensed healthcare professional.
- Aged 15-35 years.
- A physical activity level of 3/10 or higher on the Tegner Activity Scale before the injury.
- Any prior injury or condition with residual symptoms that may affect the results.
- Current injury or condition affecting the performance of the test.
- Resting pain greater than 0-1/10 on the Numeric Pain Rating Scale (NRS) and pain greater than 1-2/10 during light daily activities such as walking, sitting, standing, or climbing stairs.
Ted GunhamnStudy Responsible Party
Ted Gunhamn, Sponsor-Investigator, PhD Candidate, Linnaeus University
No contact data.
1 Study Locations in 1 Countries
Linnaues University, Kalmar, Sweden
Ted Gunhamn, Contact, +46480-4977688, [email protected]
Recruiting