Neuromuscular Training Program in Patients With Knee OA (Osteoarthritis)

NCT ID: NCT06270329

Last Updated: 2024-02-21

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

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-15

Study Completion Date

2023-06-15

Brief Summary

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The aim of this study was to compare the effects of neuromuscular training program and conventional physical therapy program on pain, functional status, physical performance, balance, muscle strength and quality of life in patients with knee osteoarthritis (KOA).

Detailed Description

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The study was carried out in Afyonkarahisar Health Sciences University Health Application Research Center in individuals with 2nd or 3rd degree KOA according to Kellgren and Lawrence Classification. The study was planned as a randomized controlled clinical trial design. The study group were recruited to the neuromuscular training program and the control group were recruited to the conventional physical therapy program 5 days a week for 3 weeks. Individuals were evaluated at the baseline and after training programs. Demographic and clinical data were first recorded in the evaluation.

Conditions

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Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

randomized controlled clinical trial design
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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neuromuscular training program

Participants were administered the neuromuscular training program 60 min a day, 2 days a week for 8 weeks.

Group Type EXPERIMENTAL

Neuromuscular training program

Intervention Type OTHER

Hotpack application TENS (transcutaneous electrical stimulation) Warm-up phase: bicycle ergometer (ten minutes)

Exercise phase:

core stabilization and postural control exercises postural orientation exercises lower extremity strengthening exercises functional exercises (balance and proprioception exercises using a balance board) Cool-down Phase

conventional physical therapy program

Participants were administered the conventional physiotherapy program 60 min a day, 2 days a week for 8 weeks.

Group Type ACTIVE_COMPARATOR

conventional physical therapy program

Intervention Type OTHER

Hotpack application TENS (transcutaneous electrical stimulation) Conventional physical therapy exercises (straight leg raises, knee flexor and extensor strengthening, hip muscle strengthening)

Interventions

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Neuromuscular training program

Hotpack application TENS (transcutaneous electrical stimulation) Warm-up phase: bicycle ergometer (ten minutes)

Exercise phase:

core stabilization and postural control exercises postural orientation exercises lower extremity strengthening exercises functional exercises (balance and proprioception exercises using a balance board) Cool-down Phase

Intervention Type OTHER

conventional physical therapy program

Hotpack application TENS (transcutaneous electrical stimulation) Conventional physical therapy exercises (straight leg raises, knee flexor and extensor strengthening, hip muscle strengthening)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Having grade 2 or 3 osteoarthritis according to the Kellgren and Lawrence Classification
* Having pain score of 2 or above on VAS
* Not having received physical therapy in the last 3 months
* Not having received an intra-articular corticosteroid injection in the last 6 months
* Not having used oral corticosteroids in the last month
* Being between the ages of 40-80
* Body mass index being between 19-40 kg/cm2

Exclusion Criteria

* Systemic arthritis
* Hypertensive condition that prevents exercise
* Pregnancy, cognitive impairment, parkinson-like neurological disorders
* Having had a knee or hip joint replacement
Minimum Eligible Age

40 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kutahya Health Sciences University

OTHER

Sponsor Role lead

Responsible Party

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Eda Ozge OKUR

Asst. Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kutahya Health Science University

Kütahya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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NMTwithKOA

Identifier Type: -

Identifier Source: org_study_id

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