Effectiveness of Neuromuscular Exercise in Patellofemoral Pain Syndrome

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-14

Study Completion Date

2024-09-11

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Patellofemoral Pain Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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control

classical physiotherapy methods

Group Type ACTIVE_COMPARATOR

control

Intervention Type OTHER

classical physiotherapy methods

exercise

In addition to classical physiotherapy methods, neuromuscular exercise protocol will be applied.

Group Type EXPERIMENTAL

Exercise

Intervention Type OTHER

In addition to classical physiotherapy methods, neuromuscular exercise protocol will be applied.

Interventions

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control

classical physiotherapy methods

Intervention Type OTHER

Exercise

In addition to classical physiotherapy methods, neuromuscular exercise protocol will be applied.

Intervention Type OTHER

Eligibility Criteria

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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.

Minimum Eligible Age

30 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes