Status:
NOT_YET_RECRUITING
The Effect of Progressive Relaxation Exercises on Postoperative Pain
Lead Sponsor:
Bartın Unıversity
Conditions:
Arthroplasty
Replacement
Eligibility:
All Genders
18-90 years
Phase:
NA
Brief Summary
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...
Detailed 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. Tot...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
December 9 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2025
Estimated Enrollment :
96 Patients enrolled
Trial Details
Trial ID
NCT05971641
Start Date
December 9 2024
End Date
September 1 2025
Last Update
July 30 2024
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