Impact of Breathing and Yoga Poses on Kinesiophobia in Knee Osteoarthritis Patients

December 30, 2025 updated by: Snekha V, Saveetha University

Effectiveness of Deep Breathing and Three Typical Yoga Poses for Kinesiophobia Among Knee Osteoarthritis Patients

The study aimed to determine if deep breathing and conventional physiotherapy were more effective than yoga poses and conventional physiotherapy in reducing kinesiophobia among knee osteoarthritis patients. 40 participants were divided into an experimental and control group, with the experimental group receiving deep breathing exercise and conventional physiotherapy, and the control group receiving yoga poses and conventional physiotherapy.

Study Overview

Detailed Description

Osteoarthritis is a degenerative joint disease causing severe pain, stiffness, and functional limitations. It involves synovial proliferation, cartilage degeneration, and structural joint changes. Knee OA is influenced by age, limb use, injury, mechanical stress, genetics, and metabolic factors, with varied clinical presentations. The knee is a complex joint made of the femoropatellar and medial/lateral femorotibial joints. It functions as a condylar synovial joint with tibial and femoral condyles, and also includes menisci that divide the joint space, increasing complexity.

Women are more likely to develop OA, with the knee being the most commonly affected. Around 344 million people require rehabilitation for OA. With rising obesity and injury rates, global OA prevalence is expected to increase. In India, OA rates differ significantly between rural and urban regions. Daily function in OA is affected not only by physical damage but also by psychological factors. Fear and avoidance behaviors can worsen pain, contributing to kinesiophobia and negatively impacting mobility.

Kinesiophobia is an excessive fear of movement or reinjury due to beliefs about pain or harm. It occurs in conditions like shoulder pain, chronic low back pain, and aging. The Tampa Scale for Kinesiophobia (TSK) is used to assess this fear.

Deep breathing relaxation techniques, including slow inhalation, breath-holding for ~5 seconds, and gentle exhalation, help reduce anxiety by relaxing supporting muscles. Deep breathing promotes emotional control, calmness, better metabolism, and regulates pain and mood through autonomic pathways.

Deep, slow breathing (DSB) can reduce pain, improve mood, and enhance sleep in healthy individuals and OA patients. It is cost-effective, calming, and may reduce joint tension, encouraging better participation in physical activity. Yoga, a mind-body practice with roots in India, enhances balance, coordination, mood, strength, flexibility, and range of motion. Pranayama (breathing) and asanas (postures) together improve both physical and mental well-being. It is considered safe for people of all ages.

Physiotherapy and exercise have been used for nearly a century to treat knee osteoarthritis. They are the second most prescribed treatment after medication. However, the long-term effectiveness and benefits of supervised, home-based, or independent exercise remain uncertain.

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Tamil Nadu
      • Chennai, Tamil Nadu, India, 602105
        • Saveetha Institute of Medical and Technical Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age: 40 - 60
  • Documented diagnosis of Osteoarthritis
  • Tampa scale Score =<68
  • Pain severity score 7-10(severity) on Visual Analog Scale
  • Short-form McGill Pain Questionnaire (SF-MPQ-2): =<220

Exclusion Criteria:

  • Severe Joint Deformity or Instability
  • Recent Surgery or Injury
  • Severe Range of Motion (ROM) Limitations
  • Neurological Conditions
  • Cardiovascular or Respiratory Conditions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Deep Breathing technique and conventional physiotherapy
Participants received Deep Breathing exercise and conventional physiotherapy for five times per week for four weeks with rest periods.
The participants are seated on chair were given a 3-min, 6 deep breaths per minute along with the Conventional physiotherapy protocol 5 times a week for 4 weeks.
Other Names:
  • Conventional physiotherapy
Active Comparator: Three Yoga poses and conventional physiotherapy
Participants received Three Typical yoga poses and conventional physiotherapy for five days each, for a total of four weeks with rest periods.
The participants were asked to perform three typical yoga poses on yoga mat along with the Conventional physiotherapy protocol 5 times a week for 4 weeks.
Other Names:
  • Conventional physiotherapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Tampa scale for kinesiophobia
Time Frame: Baseline and week 4
Tampa scale is a 17-item self-reported instrument used to distinguish between non-excessive fear and phobia in patients with chronic musculoskeletal pain, i.e., the fear of movement. Each item is a 4 -point scale anchored from 1 (strongly disagree) to 4 (strongly agree) with total score of 68. The Score 17 and below representing (no kinesiophobia) and for a participants from score 37- 68 (represents kinesiophobia).
Baseline and week 4

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual Analogue Scale
Time Frame: Baseline and week 4
The Visual Analogue Scale is a widely used tool for measuring pain severity, with endpoints ranging from "no pain" to "worst pain imaginable." Patients mark points on the scale, and clinicians track changes over time.
Baseline and week 4

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short-form McGill Pain Questionnaire (SF-MPQ-2)
Time Frame: Baseline and week 4
The Short-form McGill Pain Questionnaire-2 is a modified version of the original SF-MPQ, assessing pain in patients with various conditions. It comprises 22 descriptors rated on a 0-10 scale, providing a comprehensive evaluation of pain. The Short Form McGill Pain Questionnaire 2 (SF-MPQ-2) has demonstrated strong internal validity.
Baseline and week 4

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Madhanraj Sekar, MPT, Saveetha Institute of Medical and Technical Sciences

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 20, 2024

Primary Completion (Actual)

March 14, 2025

Study Completion (Actual)

April 24, 2025

Study Registration Dates

First Submitted

December 15, 2025

First Submitted That Met QC Criteria

December 30, 2025

First Posted (Actual)

January 8, 2026

Study Record Updates

Last Update Posted (Actual)

January 8, 2026

Last Update Submitted That Met QC Criteria

December 30, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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