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The Effectiveness of Progressive Relaxation Exercises

Not Applicable
Completed
Conditions
Functional Outcomes
Muscle Strength
Interventions
Other: progressive muscle relaxation exercise
Other: standard postoperative physiotherapy program
Registration Number
NCT04038918
Lead Sponsor
Dokuz Eylul University
Brief Summary

The purpose of this study is to investigate the effectiveness of progressive muscle relaxation (PMR) exercise on pain, functional outcomes and muscle strength in patients with TKA. Seventy patients with TKA are going to randomly assigned to intervention group and control group.

Detailed Description

Total knee arthroplasty (TKA) is applied in end-stage osteoarthritis to reduce pain, improve functional ability, and provide greater health related quality of life. However, evidence showed that presence of severe pain, impaired functional outcomes and reduced muscle strength continue up to 6 to 12 month after surgery. Relaxation techniques such as progressive muscle relaxation exercise and rhythmic breathing have long been used in treating postoperative pain and for various health-related purposes. Although the number of studies that include relaxation techniques in treating postoperative pain is increasing, there isn't any study that investigate the effectiveness of progressive muscle relaxation exercise on pain, functional outcomes and muscle strength in patients with TKA.

The aim is to investigate the effectiveness of progressive muscle relaxation (PMR) exercise on pain, functional outcomes and muscle strength in patients with TKA.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
106
Inclusion Criteria
  • 30 years older above
  • Preoperative diagnosis have to be knee osteoarthritis
  • Have a primary total knee arthroplasty
  • Able to understand Turkish instructions
  • Willing and able to attend study
Exclusion Criteria
  • Revision total knee arthroplasty
  • Unable to understand verbal and written instructions
  • Having previously orthopaedic or neurological disorder that causes gait disturbance

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Progressive Muscle Relaxation Exercise Groupprogressive muscle relaxation exerciseStandard postoperative physiotherapy program plus progressive muscle relaxation (PMR) exercise will be applied.
Control Groupstandard postoperative physiotherapy programStandard postoperative physiotherapy program will be applied.
Progressive Muscle Relaxation Exercise Groupstandard postoperative physiotherapy programStandard postoperative physiotherapy program plus progressive muscle relaxation (PMR) exercise will be applied.
Primary Outcome Measures
NameTimeMethod
The Numeric Pain Rating ScalePostoperative three months

The Numeric Rating Scale (NPRS), reliable and valid instrument, is commonly used to determine for pain intensity in rehabilitation. The activity and resting pain level in the knee joints will be evaluated by NPRS from 0 to 10 (0 refers to no pain, 10 refers to worst pain).

Muscle StrengthPostoperative three months

Strength of knee muscles will be evaluated by hand-held dynamometer.

Hospital for Special Surgery Knee ScorePostoperative three months

Hospital for Special Surgery knee score. A scoring system evaluation of pain, mobility, range of motion and deforming of the knee giving 0-100 points.

Iowa Level of Assistance ScalePostoperative three months

This test assesses the patient's ability to perform four functional activities, namely, supine to sitting on the edge of the bed, sitting on the edge of the bed to standing, walking 4.57 meters. The scoring of these activities is done as independent 6 points, observational aid 5 points, minimum help 4 points, medium help 3 points, maximum help 2 points, fail 1 point and untested 0 points. Higher values represent a better outcome.

Speed scoring is done by evaluating the walking speed at a distance of 13.4 meters (44 steps). 20 seconds (sec) and below are recorded as 0, 21-30 sec 1, 31-40 sec 2, 41-50 3, 51-60 sec 4, 61-70 sec 5 and 70 sec. Higher values represent a worse outcome

10 meter walk speed testPostoperative three months

10MWT testing distance require 5-m acceleration and 5-m deceleration space, with the inner 10-m zone being the distance over which gait is timed. Before the test, patients should be asked to walk as fast as possible and allowed to use assistive devices (cane, walker) if needed. Patients start to walk and accelerate in the 20-m. The stopwatch is started as soon as the patient's leg pass over the starting line and stopped the patient's leg pass over the 10-m sign.

Timed Up and Go (TUG)Postoperative three months

To determine fall risk and measure the progress of balance, sit to stand, and walking. The patient starts in a seated position. The patient stands up upon therapist's command walks 3 meters, turns around, walks back to the chair and sits down. The time stops when the patient is seated. The subject is allowed to use an assistive device.

Secondary Outcome Measures
NameTimeMethod
12-Item Short Form SurveyPostoperative three months

SF-12 Health Survey is a shorter version of the SF-36 Health Survey that uses just 12 questions to measure functional health and well-being from the patient's point of view. The SF-12 is a practical, reliable and valid measure of physical and mental health and is particularly useful in large population health surveys or for applications that combine a generic and disease-specific health survey.

Range of MotionPostoperative three months

Each patient's active (unassisted) range of knee extension and flexion will be measured, using a goniometer with the patient in the supine position.

Tampa Scale for Kinesiophobia (TSK)Postoperative three months

The term kinesiophobia refers to a fear of pain with movement - i.e., movements which a patient is hesitant to perform due to fear that the movement will elicit pain. The TSK has been used to assess kinesiophobia in patients with a wide variety of conditions, such as knee disorders. The TSK consists of 17 questions. A score of 17 is the lowest possible score, and indicates no kinesiophobia or negligible. A score of 68 is the highest possible score and indicates extreme fear of pain with movement.

The Hospital Anxiety and Depression Scale (HADS)Postoperative three months

The HADS aims to measure symptoms of anxiety and depression and consists of 14 items, seven items for the anxiety subscale (HADS Anxiety) and seven for the depression subscale (HADS Depression). Each item is scored on a response-scale with four alternatives ranging between 0 and 3. After adjusting for six items that are reversed scored, all responses are summed to obtain the two subscales. The scoring of HADS is done as normal 0-7 point, borderline case 8-10 points, abnormal case 11-21. Higher values represent a worse outcome.

Trial Locations

Locations (1)

Dokuz Eylul University

🇹🇷

İzmir, Turkey

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