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NOT YET RECRUITING
NCT07329010
NA

Effects of Preoperative Whey Protein and Exercise Support on Recovery After Total Hip Arthroplasty

Sponsor: TC Erciyes University

View on ClinicalTrials.gov

Summary

Objective: The aim of this project is to evaluate the effects of preoperative whey protein supplementation and a physical exercise program on postoperative recovery outcomes in patients undergoing total hip arthroplasty (THA). Specifically, inflammatory markers (CRP), nutritional status (albumin), mobilization time, length of hospital stay, and physical and social functioning will be assessed. As one of the first randomized controlled trials in Turkey to focus on the preoperative period and to evaluate a combined nutrition and exercise intervention in elderly surgical patients, this study holds pioneering significance in both clinical and academic contexts. Methods: This study is designed as a randomized controlled trial. The intervention group will receive whey protein supplementation and a home-based exercise program for 14 days preoperatively, while the control group will receive standard preoperative care. Data collection will be performed preoperatively and on postoperative days 3 and 5, focusing on metabolic and functional parameters. Expected Outcomes: The findings of this study are expected to contribute to the improvement of patient care through a multidisciplinary approach, inform health policy development, and provide a foundation for larger-scale clinical research in Turkey.

Official title: The Effect of Preoperative Whey Protein and Physical Exercise Support on Recovery After Total Hip Arthroplasty

Key Details

Gender

All

Age Range

50 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2026-01

Completion Date

2026-05-30

Last Updated

2026-01-09

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

Preoperative Whey Protein and Exercise Program

The intervention group will receive 14 days of preoperative whey protein supplementation combined with a home-based exercise program. Patients will receive face-to-face instructions at program initiation, and data will be collected under the supervision of an experienced orthopedic surgeon