Actively Recruiting
Effect of Foot Massage on Pain and Analgesic Consumption in Total Knee Prosthesis
Led by Alev Keskin · Updated on 2025-12-16
60
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This randomized controlled trial aims to examine the effects of foot massage combined with cold application on postoperative pain, patient satisfaction, and analgesic consumption in individuals undergoing Total Knee Arthroplasty (TKA). The study will be conducted in the Orthopedics and Traumatology Department of Çukurova University Balcalı Hospital, which includes an 18-bed orthopedic unit. Eligible patients will be randomly assigned to either the intervention group or the control group. * Intervention group: Patients will receive both cold application and foot massage. Cold therapy will be administered for 20 minutes every 2 hours for the first 48 hours postoperatively. Foot massage will be performed twice daily (morning and evening) for two days following drain removal, using standardized massage techniques. * Control group: Patients will receive only cold application following the same schedule and procedure as the intervention group. Data will be collected using the Patient Information Form, the Short Form of the Brief Pain Inventory, the Numeric Rating Scale, and the Newcastle Satisfaction with Nursing Care Scale. Statistical analyses will be conducted using SPSS, and findings will be interpreted at a 95% confidence level (p \< 0.05). Ethical approval has been granted by the Çukurova University Non-Interventional Clinical Research Ethics Committee. Institutional permission will be obtained prior to data collection. Participation will be voluntary, and all data will be treated confidentially.
CONDITIONS
Official Title
Effect of Foot Massage on Pain and Analgesic Consumption in Total Knee Prosthesis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Being 18 years or older
- Ability to speak Turkish
- No visual or hearing impairment
- No cognitive disability
- Undergoing unilateral knee replacement surgery
- Volunteering to participate in the study
You will not qualify if you...
- Presence of any intellectual disability or psychiatric disorder
- History of diabetes
- Presence of neurological or cerebrovascular disease
- Diagnosis of deep vein thrombosis
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Çukurova Üniversitesi
Adana, University, Turkey (Türkiye)
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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