Exploring the Relationship Between Range of Motion in Knee Rehabilitation Exercises and Pain in Patellofemoral Pain Syndrome

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age15-35
SponsorTed Gunhamn

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial population

This project will include patients diagnosed with PFP (ICD-10: M22.2).

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • Exercise

    Other intervention

    Exercise with progressively increased range of motion.

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: Patellofemoral Pain Syndrome1 intervention

Trial outcomes

Primary outcomes

1

Pain (VAS)

Pain measured 0-10 visual analog scale (VAS) reported during each trial of progressively increased range of motion during a single session.

Time frame
Day 1 (Cross sectional single session. Outcomes will be collected during one single session for each participant.)
2

Range of motion

Degrees of knee flexion measured during each trial in one single session.

Time frame
Day 1 (Cross sectional single session. Outcomes will be collected during one single session for each participant.)

Secondary outcomes

1

Force

Force (N) (peak value) reported during the different trials in one session. Measured by force plates.

Time frame
Day 1 (Cross sectional single session. Outcomes will be collected during one single session for each participant.)
2

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.

Time frame
Baseline (Administered at the beginning of the study)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ted Gunhamn

Lead sponsor

Linnaeus University

Sponsor institution