NCT07139158

Brief Summary

Patellofemoral joint problems account for a significant portion of knee pain and disability. Among these problems, patellofemoral pain is not directly related to any obvious structural abnormality and is characterized by pain in the retro- or peri-patellar region, particularly during activities such as squatting, running, and climbing stairs. It is commonly seen in the general population. The current literature highlights the tendency of patellofemoral pain to recur and become chronic despite all treatments. Individuals with patellofemoral pain often experience disorders in the neuromuscular function of the quadriceps femoris muscle, which is necessary for knee function and dynamic stability and is frequently suggested to play an important role in the pathophysiology of the disease. A decrease in the tissue's ability to utilize oxygen during exercise or physical activity may lead to permanent dysfunction of the quadriceps femoris muscle. However, no studies have been found in the literature examining changes in oxygenation of the quadriceps femoris muscle in individuals with patellofemoral pain. Therefore, the aim of this study is to investigate changes in oxygenation of the quadriceps femoris muscle in individuals with patellofemoral pain during various exercises and physical activities by comparing them with pain-free individuals.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
41

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Aug 2025

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 17, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

August 20, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 24, 2025

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2025

Completed
Last Updated

February 10, 2026

Status Verified

August 1, 2025

Enrollment Period

11 days

First QC Date

August 17, 2025

Last Update Submit

February 6, 2026

Conditions

Keywords

patellofemoral painnear-infrared spectroscopylower extremitykinesiophobiaphysical activity

Outcome Measures

Primary Outcomes (1)

  • Muscle Oxygenation

    Vastus medialis muscle oxygenation will be evaluated with Near-Infrared Spectroscopy at rest, during and after activity.

    Day 1

Secondary Outcomes (5)

  • Kujala Patellofemoral Score Scale

    Day 1

  • International Physical Activity Questionnaire (IPAQ)

    Day 1

  • Adipose tissue thickness

    Day 1

  • Numeric Pain Rating Scale

    Day 1

  • Tampa Kinesiophobia Scale

    Day 1

Study Arms (2)

Patellofemoral Pain Group

Pain-free Control Group

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Twenty-one patients with patellofemoral pain and 20 pain-free controls will be conducted at Ankara Medipol University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Department.

You may qualify if:

  • years of age
  • pain around or behind the patella, which is aggravated by at least one activity that loads the patellofemoral joint during weight bearing on a flexed knee (e.g., squatting, stair ambulation, jogging/running, hopping/jumping)
  • the pain persist for at least four months, and be rated at ≥ 3/10 on the Numeric Pain Rating Scale (NPRS)
  • vastus medialis muscle adipose tissue thickness \<20 mm
  • Pain-free controls were age- and gender-matched, with vastus medialis muscle adipose tissue thickness \<20 mm.

You may not qualify if:

  • a history of joint surgery
  • meniscal and/or ligament injuries
  • patellar instability, congenital patellar subluxation/dislocation
  • any cardiovascular, congenital, or musculoskeletal disorders that could interfere with the assessment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Medipol University

Ankara, Altındağ, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Patellofemoral Pain SyndromeKinesiophobiaMotor Activity

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesPhobic DisordersAnxiety DisordersMental DisordersBehavior

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

August 17, 2025

First Posted

August 24, 2025

Study Start

August 20, 2025

Primary Completion

August 31, 2025

Study Completion

August 31, 2025

Last Updated

February 10, 2026

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations