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The Effect of Progressive Relaxation Exercises on Postoperative Pain

B

Bartın Unıversity

Status

Not yet enrolling

Conditions

Arthroplasty
Knee
Replacement

Treatments

Other: progressive relaxation exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT05971641
Bartın U

Details and patient eligibility

About

The indicators of patient recovery in the postoperative period include sleep, physical functionality, mental health, cognitive functionality, pain, and psychosocial functionality.

This thesis aims to investigate the effects of progressive relaxation exercises on postoperative pain intensity, sleep quality, and recovery in patients undergoing total knee arthroplasty.This study, designed as a randomized controlled experimental study, will be conducted between September 1, 2023, and August 1, 2024, at ÇAYCUMA State Hospital in ZONGULDAK province, Turkey, among patients undergoing total knee arthroplasty. A total of 96 patients will be recruited based on the sample size calculated using G-power analysis. Through block randomization, 48 patients will be assigned to the intervention group and 48 patients to the control group. Data will be collected using the Numeric Rating Scale for pain, the Richard-Campbell Sleep Scale, a sleep tracker smart wristband to measure sleep quality and duration, the Postoperative Recovery Index, and a Patient Information Form.

Full description

Introduction: Knee osteoarthritis is observed in approximately 6% of adult individuals. Knee osteoarthritis, which causes pain in individuals, often results in the impairment of their daily lives. Total knee arthroplasty surgery is considered as the final method in the treatment process of knee osteoarthritis. The indicators of patient recovery in the postoperative period include sleep, physical functionality, mental health, cognitive functionality, pain, and psychosocial functionality.

Objective: This thesis aims to investigate the effects of progressive relaxation exercises on postoperative pain intensity, sleep quality, and recovery in patients undergoing total knee arthroplasty.

Method: This study, designed as a randomized controlled experimental study, will be conducted between September 1, 2023, and August 1, 2024, at ÇAYCUMA State Hospital in ZONGULDAK province, Turkey, among patients undergoing total knee arthroplasty. A total of 96 patients will be recruited based on the sample size calculated using G-power analysis. Through block randomization, 48 patients will be assigned to the intervention group and 48 patients to the control group. Data will be collected using the Numeric Rating Scale for pain, the Richard-Campbell Sleep Scale, a sleep tracker smart wristband to measure sleep quality and duration, the Postoperative Recovery Index, and a Patient Information Form. The progressive relaxation exercises Compact disc 8 (CD) prepared by the Turkish Psychologists Association will be used for the patients' progressive relaxation exercise training. The data will be analyzed using the Statistical Package for the Social Sciences (SPSS) program. The data will be presented as numbers and percentages, means and standard deviations, and their distribution will be assessed to determine whether parametric or non-parametric tests should be employed for analysis. The data will be evaluated with a significance level of p<0.05 and a confidence interval of 95%.

Enrollment

96 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years and older,
  • Without diagnosed mental disorders,
  • Without visual, hearing, and speech impairments,
  • Proficient in Turkish,
  • Diagnosed with gonarthrosis and scheduled for total knee replacement,
  • No postoperative complications following total knee replacement surgery,
  • Literate with an educational level,
  • Pain level of 4 or above on the NRS,
  • Receiving analgesic treatment according to the clinical protocol,
  • Ownership of a mobile device such as a smart phone or tablet capable of accessing internet-based video content with the latest technology from any brand,
  • Patients without diagnosed sleep problems will be included in the thesis study.

Exclusion criteria

  • Illiterate individuals,
  • Under the age of 18,
  • Having a condition that hinders communication,
  • Referred from another center after surgery,
  • Pain level of 4 or below on the NRS,
  • Developing complications after total knee replacement surgery,
  • Receiving analgesic treatment and methods outside of the clinical protocol,
  • Not owning a mobile device such as a smart phone or tablet capable of accessing internet-based video content with the latest technology from any brand,
  • Having diagnosed sleep problems,
  • Having diagnosed mental disorders, will be excluded from the scope of the thesis study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

96 participants in 2 patient groups

intervention group
Active Comparator group
Description:
The experimental group is the one in which progressive relaxation exercises will be taught, and we will monitor the results in patients.
Treatment:
Other: progressive relaxation exercise
control group
No Intervention group
Description:
The control group is the one in which the service routine is implemented, and progressive relaxation exercises are not taught but monitored.

Trial contacts and locations

0

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Central trial contact

Rumeysa Birkanım, Msc student; Sevim Çelik, Professor

Data sourced from clinicaltrials.gov

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