Effect of Whole Body Vibration Therapy on Pain, Muscle Strength, Balance and Quality of Life in Knee Osteoarthritis

NCT ID: NCT06542692

Last Updated: 2024-08-07

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

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-08-28

Study Completion Date

2023-12-28

Brief Summary

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The aim of this study is to examine the effects of whole body vibration therapy on knee osteoarthritis. While the participants did static exercise in one group, whole body vibration therapy was applied during static exercise in another group. As a result of 15 sessions of treatment in both groups, the effects on pain, muscle strength, balance and quality of life were compared.

Detailed Description

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Conditions

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Osteoarthritis, Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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study group

Whole body vibration therapy added group

Group Type EXPERIMENTAL

Whole Body Vibration

Intervention Type DEVICE

treatment duration, frequency

physical therapy modalities

Intervention Type DEVICE

ultrasound, hot pack, tens

control group

Group Type EXPERIMENTAL

physical therapy modalities

Intervention Type DEVICE

ultrasound, hot pack, tens

Interventions

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Whole Body Vibration

treatment duration, frequency

Intervention Type DEVICE

physical therapy modalities

ultrasound, hot pack, tens

Intervention Type DEVICE

Other Intervention Names

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physical therapy modalities

Eligibility Criteria

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Inclusion Criteria

* Those who were diagnosed with primary symptomatic knee OA according to ACR criteria,Ages between 35 and 70, Body mass index (BMI) ⩽35, Grade II or III according to Kellgren \& Lawrence scale, Patients with persistent symptoms such as pain and stiffness for at least 3 months were included.

Exclusion Criteria

* Those who have had knee surgery before, Those with central nervous system disease (especially epilepsy and serious psychotic disorders), those with a history of acute arthritis, Those with a history of DVT in the last 24 weeks, Those with advanced lung or heart disease (COPD and heart failure), Those diagnosed with inflammatory rheumatic diseases (Rheumatoid arthritis, Spondyloarthropathy, etc.), Patients diagnosed with advanced stage cancer were excluded from the study.
Minimum Eligible Age

35 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Burak Çetinkaya

OTHER

Sponsor Role lead

Responsible Party

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Burak Çetinkaya

principal investigator

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Kocaeli University

Kocaeli, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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E68869993-511.06.01.01-1193507

Identifier Type: -

Identifier Source: org_study_id

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