Skip to main content
OpenTrials
Completed

NCT Number: NCT04845204

Relaxation Treatment in Total Knee Arthroplasty

Surgical techniques and treatment methods of the arthroplasty have been improved and the results after total knee arthroplasty (TKA) are generally good. However, some patients have suboptimal postoperative results with respect to pain and physical functioning and may not be satisfied with the results of their TKA. Psychological symptoms were found to be associated with these suboptimal results. The aim of the present study is to determine weather relaxation techniques had beneficial effects on pain, sleeping quality, functional status and physiological symptoms in TKA patients during their hospital stay.

Completed

Looking for future studies?

Notify Me

Key information

Age range

55 year–75 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • primary knee osteoarthritis, Female Patients who are scheduled for unilateral Total Knee Arthroplasty surgery, were included in the study.

Exclusion criteria

  • having a previous knee or hip surgery or fracture, diagnosis of rheumatoid arthritis, severe obesity (BMI>40 kg/m2), sensory and motor disorders in the operated limb, inability to understand pain assessment.

Treatment and study plan

Relaxation Treatment

Other

Relaxation Group recieve progressive muscle relaxation exercises additional to the standard exercises. The relaxation exercises are applied two times a day till the discharge day starting on the postoperative day one. Progressive muscle relaxation included the relaxing of different muscle groups along with deep breathing. The maximal contraction period consist of the contraction of muscle groups around ankle, calf, knee, hip, lumbar, thoracic and cervical regions, shoulder, arm, forearm for 5 s and continued with a relaxation period for 30 s while focusing on breathing. These two periods ware repeated for each muscle groups and lasted approximately 30 min

Other names: Standard Exercises

Standard Exercises

Other

The physiotherapy protocol is applied under the supervision of the same physiotherapist within a progressive manner immediately after surgery. Continued passive range of motion is applied twice a day starting with 45º of knee flexion range of motion and increased gradually as tolerated. All patients performed same isometric, isotonic and active exercises. Patients were instructed to bear weight as tolerated on the postoperative day 1

Other names: Relaxation Treatment

Primary outcomes

  1. Pain Level Change

    Time frame: Mean change from Postoperative day 1 to day 4 recorded

    Visual analog scale

Secondary outcomes

  1. Sleep Quality Change

    Time frame: Mean change from Postoperative day 1 to day 4 recorded

    Visual analog scale

  2. Functional Outcomes Change

    Time frame: Mean change from Postoperative day4 to 6 weeks following surgery recorded

    Timed Up and Go

  3. Functional Outcomes Change

    Time frame: Mean change from Postoperative day4 to 6 weeks following surgery recorded

    Western Ontario McMaster Universities Osteoarthritis Index (WOMAC)

  4. Knee Range of Motion Change

    Time frame: Mean change from Postoperative day4 to 6 weeks following surgery recorded

    Flexion and Extension

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Registry information

Official study title

Effects of Progressive Muscle Relaxation Techniques on Pain, Sleeping Quality and Functional Levels After Total Knee Arthroplasty

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Apr 14, 2021
Registry last updated
Apr 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.