Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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 0-10 Visual Analog Scale (VAS) until either (1) achieving full depth in the respective exercise or (2) reaching a pain level of >5 on the VAS.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patellofemoral Pain Syndrome | Patients diagnosed with patellofemoral pain syndrome by health care provider. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Exercise | Other | Exercise with progressively increased range of motion. |
|
| 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.) |
| 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) |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
This project will include patients diagnosed with PFP (ICD-10: M22.2).
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Linnaues University | Recruiting | Kalmar | Sweden |
Not provided
| ID | Term |
|---|---|
| D046788 | Patellofemoral Pain Syndrome |
| ID | Term |
|---|---|
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D015444 | Exercise |
| ID | Term |
|---|---|
| D009043 | Motor Activity |
| D009068 | Movement |
| D009142 | Musculoskeletal Physiological Phenomena |
| D055687 | Musculoskeletal and Neural Physiological Phenomena |
Not provided
Not provided
Not provided
Not provided
Not provided
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) |