The Effectiveness of Resistance Training for Patients With Degenerative Arthritis After Surgery

NCT07696195 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2026-07-10

No results posted yet for this study

Summary

Osteoarthritis is a common degenerative disease that significantly impacts mobility and disability in older adults. This pilot randomized controlled study aimed to examine the effects of a three-month resistance training program on lower limb muscular endurance, balance performance, pain, and quality of life among patients who had undergone unilateral total knee arthroplasty. Twenty-four participants were randomly assigned to either the experimental group receiving resistance training or the control group receiving routine postoperative rehabilitation. The study evaluates and compares the effectiveness of these interventions to provide insights into incorporating resistance training into postoperative nursing care and recovery programs.

Conditions

Interventions

BEHAVIORAL

Progressive Lower Extremity Resistance Exercise

A 3-month progressive resistance training program utilizing 1-kg ankle weights, including seated knee extension, standing hamstring curls, and hip abduction. Training sessions were performed 3 times per week, with progressive adjustments in training volume (sets and repetitions) for both operated and non-operated limbs over the 3-month period.

BEHAVIORAL

Routine Postoperative Rehabilitation Care

Participants in the control group received routine postoperative rehabilitation care.

Sponsors & Collaborators

  • Tzu Chi University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-01
Primary Completion
2025-05-22
Completion
2025-08-19

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07696195 on ClinicalTrials.gov