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Effectiveness of Neuromuscular Exercise in Patellofemoral Pain Syndrome

U

Uskudar University

Status

Completed

Conditions

Patellofemoral Pain Syndrome

Treatments

Other: control
Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT06407414
Uskudar8

Details and patient eligibility

About

The aim of the study is to investigate the effects of a neuromuscular exercise program on strength, balance, sleep quality and functionality in individuals with Patellofemoral pain syndrome.

Full description

The research is planned as a quantitative study. Classical knee exercises will be given to 25 individuals in the control group of the study. An exercise program consisting of Neuromuscular exercises will be applied to 25 individuals in the intervention group. In data collection, strength and balance measurements will be measured face to face by a physiotherapist, and the scales to be made through a survey will be sent to the patients online and they will be asked to fill them out. The scales and forms to be used are as follows: 1.Kujala Patellofemoral Score Scale 2.Lysholm Knee Scoring Scale 3.International Physical Activity Survey 4.Pittsburgh Sleep Quality Index 5.Y Balance Test 6.30 Seconds Sit and Stand Test Applied scales will be done by the physiotherapist. The surveys will be uploaded to the Google Forms database and the participants will be contacted via e-mail or mobile phone applications (such as Whatsapp, Telegram) to participate. They will first be asked to fill out the surveys before starting the exercise program and they will be asked to apply the exercise program. It will be explained as follows. Exercises will be planned 3 times a week and for 12 weeks. Participants will be asked to participate in the survey again after completing the exercise program.

Enrollment

50 patients

Sex

All

Ages

30 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Volunteering to participate in the study.
  • Not under 30 years of age and not over 60 years of age.
  • Having patellofemoral pain syndrome.
  • Not having a physical disability.
  • Not having undergone any knee-related surgery.
  • Having access to a computer/tablet/phone and the internet.

Exclusion criteria

  • Not accepting the voluntary consent form.
  • Being under 30 years of age and over 60 years of age.
  • Having undergone any knee-related surgery.
  • Having cognitive, mental or psychological problems.
  • Having impaired vision or hearing.
  • Having a physical condition that causes significant loss of function.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

control
Active Comparator group
Description:
classical physiotherapy methods
Treatment:
Other: control
exercise
Experimental group
Description:
In addition to classical physiotherapy methods, neuromuscular exercise protocol will be applied.
Treatment:
Other: Exercise

Trial contacts and locations

1

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Central trial contact

Ömer ŞEVGİN

Data sourced from clinicaltrials.gov

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