Status:
NOT_YET_RECRUITING
Effects of Stress Ball and Hand Holdig on Pain and Mobility Levels During Continuous Passive Motion In Patients With Total Knee Prosthesis: A Randomized Controlled Trial
Lead Sponsor:
Necmettin Erbakan University
Conditions:
Pain and Mobility Levels of Patients Undergoing Total Knee Prosthesis During Continuous Passive Motion Exercise
Eligibility:
All Genders
Phase:
NA
Brief Summary
Pain after Total Knee Prosthesis (TKA) is an important problemWhen pain is not controlled, it can negatively affect the patients\' mobility level.This research; A randomized controlled...
Detailed Description
Type of research:This study was planned as a randomized controlled experimental design to investigate the effects of stress ball and hand holding on pain and mobility levels during continuous passive ...
Eligibility Criteria
Inclusion
- After being informed about the study, written permission was obtained for voluntary participation
- Ages 18 and over
- In the preoperative evaluation, ASA scores were at levels I and II.
- Able to speak Turkish and communicate verbally
- A combination of spinal anesthesia and adductor block was applied during the surgery.
- first time and unilateral total knee prosthesis was performed
- Total knee prosthesis surgery is performed by the same physician and the same surgical technique
- Patients who underwent continuous passive movement exercise after removing the hemovac drain on the first day after surgery were planned to be included in the study.
Exclusion
- Alzheimer\'s, dementia-like conditions that prevent understanding
- Analgesic was administered outside of the analgesic treatment plan determined before continuous passive movement exercise.
- General anesthesia or a different anesthesia is applied during the surgery.
- Patients who stay in the recovery unit for more than 1 hour (more than the routine period) after surgery or who receive treatment and care in the intensive care unit (patients whose vital signs are unstable, who develop lung problems, who are bleeding, who require blood transfusion, who have severe pain)
- Describing pain outside the surgical area
- In the preoperative evaluation, it was planned that patients with ASA scores of III, IV and V would not be included in the study.
Key Trial Info
Start Date :
September 25 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 25 2025
Estimated Enrollment :
78 Patients enrolled
Trial Details
Trial ID
NCT06608264
Start Date
September 25 2024
End Date
December 25 2025
Last Update
September 23 2024
Active Locations (1)
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1
Aksaray Training and Research Hospital [Aksaray Eğitim ve Araştırma Hastanesi]
Aksaray, Aksaray/center, Turkey (Türkiye), 68200