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Clinical Trials/NCT07411027
NCT07411027
Not yet recruiting
Not Applicable

The Effects of Body Awareness-Based Sensorimotor Rehabilitation on Physical Psychosocial Status in Patellofemoral Pain Syndrome

Recep Tayyip Erdogan University1 site in 1 country60 target enrollmentStarted: February 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Recep Tayyip Erdogan University
Enrollment
60
Locations
1
Primary Endpoint
Pain Behavior Score

Overview

Brief Summary

Patellofemoral pain syndrome is a common knee condition that causes pain around or behind the kneecap, especially during activities such as walking, climbing stairs, squatting, or prolonged sitting. This condition can affect daily activities, movement quality, and psychological well-being.

The purpose of this study is to investigate the effects of a body awareness-based sensorimotor rehabilitation program on pain behavior, movement quality, and psychosocial outcomes in individuals with patellofemoral pain syndrome.

Participants will be randomly assigned to either an intervention group receiving body awareness-based sensorimotor rehabilitation or a control group receiving conventional physiotherapy exercises. The rehabilitation program will focus on improving body awareness, posture, balance, and controlled movement patterns.

Outcomes will be assessed before and after the intervention period. The main outcomes include changes in pain-related behaviors, movement quality, and psychosocial status.

The results of this study are expected to provide evidence on whether body awareness-based sensorimotor rehabilitation can be an effective approach for managing patellofemoral pain and improving both physical and psychological aspects of function.

Detailed Description

This study is designed as a randomized controlled clinical trial to investigate the effects of a body awareness-based sensorimotor rehabilitation program on pain behavior, movement quality, and psychosocial outcomes in individuals with patellofemoral pain syndrome.

Eligible participants diagnosed with patellofemoral pain syndrome will be randomly allocated to either an intervention group or a control group. Randomization will be performed using a computer-generated sequence.

The intervention group will receive a structured body awareness-based sensorimotor rehabilitation program. This program will focus on improving body awareness, postural control, balance, and coordinated movement through guided exercises and movement education. The program aims to enhance participants' ability to perceive and control their body movements during functional activities.

The control group will receive conventional physiotherapy exercises commonly used in the management of patellofemoral pain syndrome. These exercises will focus on strengthening, flexibility, and functional training.

Both groups will participate in their respective programs for a defined intervention period. Outcome assessments will be conducted at baseline and at the end of the intervention period by assessors blinded to group allocation.

Primary outcomes include changes in pain-related behaviors. Secondary outcomes include changes in movement quality and psychosocial status.

The findings of this study will contribute to understanding the role of body awareness-based sensorimotor rehabilitation in the comprehensive management of patellofemoral pain syndrome.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adults aged 18-45 years.
  • Clinical diagnosis of patellofemoral pain syndrome with anterior or retropatellar knee pain.
  • Knee pain lasting for at least 3 months.
  • Pain intensity of at least moderate level during functional activities such as stair climbing, squatting, or prolonged sitting.
  • Ability to understand and follow instructions and provide informed consent.
  • Willingness to participate in the rehabilitation program.

Exclusion Criteria

  • History of knee surgery within the past 12 months.
  • Presence of other knee pathologies (e.g., ligament injury, meniscal tear, osteoarthritis).
  • Diagnosis of inflammatory or rheumatological diseases.
  • Neurological disorders affecting balance or movement.
  • Current pregnancy.
  • Participation in another structured physiotherapy or rehabilitation program within the past 3 months.
  • Any condition that may prevent safe participation in exercise.

Arms & Interventions

Body Awareness-Based Sensorimotor Rehabilitation

Experimental

Participants in this group will receive a structured body awareness-based sensorimotor rehabilitation program. The program will consist of guided exercises focusing on increasing body awareness, postural control, balance, and coordinated movement patterns.

The intervention aims to enhance participants' ability to perceive, interpret, and control their body movements during functional activities. Exercises will emphasize controlled movement, alignment, breathing, and proprioceptive feedback.

The rehabilitation sessions will be supervised by a physiotherapist and will be delivered over a defined intervention period.

Intervention: Sensorimotor Rehabilitation (Other)

Body Awareness-Based Sensorimotor Rehabilitation

Experimental

Participants in this group will receive a structured body awareness-based sensorimotor rehabilitation program. The program will consist of guided exercises focusing on increasing body awareness, postural control, balance, and coordinated movement patterns.

The intervention aims to enhance participants' ability to perceive, interpret, and control their body movements during functional activities. Exercises will emphasize controlled movement, alignment, breathing, and proprioceptive feedback.

The rehabilitation sessions will be supervised by a physiotherapist and will be delivered over a defined intervention period.

Intervention: Conventional Physiotherapy Exercise Program (Other)

Control

Active Comparator

Participants in this arm will receive a conventional physiotherapy exercise program focusing on general strengthening, flexibility, balance, and functional movement exercises. The program reflects standard clinical practice and does not include structured body awareness-based components. Sessions will be supervised by a physiotherapist and delivered with the same frequency and duration as the experimental group.

Intervention: Conventional Physiotherapy Exercise Program (Other)

Outcomes

Primary Outcomes

Pain Behavior Score

Time Frame: Baseline (Week 0) and Post-intervention (Week 8)

Pain behavior refers to observable and self-reported behaviors related to pain experience, including pain intensity, pain-related avoidance, and functional responses to pain during daily activities. In this study, pain behavior will be evaluated to determine the effect of the intervention on participants' pain-related responses and functional adaptation. Pain-related behavior will be assessed using the Turkish Pain Behavior Questionnaire total score to evaluate changes in pain-related responses and avoidance behaviors.

Movement Quality Assessment Scale Total Score

Time Frame: Baseline (Week 0) and Post-intervention (Week 8)

Movement quality refers to the efficiency, control, and coordination of body movements during functional activities. In this study, movement quality will be assessed to evaluate changes in postural control, balance, and coordinated movement patterns as a result of the rehabilitation program. Movement quality will be assessed using a standardized movement quality assessment scale evaluating postural control, balance, and coordinated movement patterns.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Recep Tayyip Erdogan University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Seda Karaca

Dr

Recep Tayyip Erdogan University

Study Sites (1)

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