Guneysu Physical Therspy and Rehabilitation School
Rize, Turkey (Türkiye)
NCT Number: NCT07411027
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.
Trial opening soon.
Get Notified18 year–45 year
All sexes
Interventional
Not applicable
Rize, Turkey (Türkiye)
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Sensorimotor rehabilitation is a physiotherapy approach that aims to improve the integration of sensory input and motor output to enhance movement control and functional performance. It focuses on optimizing how the nervous system processes sensory information (such as proprioception, balance, and tactile input) to produce efficient and coordinated movements.
This approach includes exercises that target postural control, balance, joint position sense, and neuromuscular coordination. The main goal is to restore normal movement patterns, reduce compensatory strategies, and improve functional stability during daily and sports-related activities.
Sensorimotor rehabilitation is commonly used in the management of musculoskeletal conditions, particularly those involving movement dysfunction, pain, and impaired motor control, such as knee pain and patellofemoral pain syndrome.
A structured conventional physiotherapy exercise program including strengthening, flexibility, balance, and functional movement exercises based on standard rehabilitation principles. The program is supervised by a physiotherapist and applied according to routine clinical exercise protocols.
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.
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.
Contact information is provided by the study sponsor or research team.
Recep Tayyip Erdogan University
Other
The Effects of Body Awareness-Based Sensorimotor Rehabilitation on Physical Psychosocial Status in Patellofemoral Pain Syndrome
Acronym: BASPR-PFP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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