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Not Yet RecruitingNCT06983912

Preoperative Rehabilitation Training and Total Knee Arthroplasty Outcomes

The Effect of Preoperative Rehabilitation on Functional Recovery After Total Knee Arthroplasty: A Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Fuzhou University Affiliated Provincial Hospital · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Joint replacement surgery is an effective treatment for severe joint diseases, but the postoperative recovery process is complex and lengthy. Preoperative rehabilitation training, as an important part of preoperative preparation, has been proven to significantly improve postoperative recovery outcomes. However, there is currently a lack of systematic research on the optimal protocols and duration of preoperative rehabilitation training and their specific impacts on postoperative recovery. This study aims to evaluate the effects of preoperative rehabilitation training on postoperative recovery after joint replacement through a randomized controlled trial, providing scientific evidence for clinical practice.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPreoperative Rehabilitation TrainingInitiate preoperative Physical Rehabilitation Training (PRT) starting from the preoperative period, with training five days a week up until the day before surgery. This includes: Muscle Strength Training: Isometric contractions of the quadriceps, straight leg raises, etc., for 15-20 minutes per session, twice daily. Joint Mobility Training: Flexion and extension exercises of the knee joint, ankle pump exercises, etc., for 10-15 minutes per session, twice daily. Balance Training: One-legged standing, center of gravity shifting exercises, etc., for 10-15 minutes per session, twice daily. Activities of Daily Living Training: Transfer training from sitting to standing, walking exercises, etc., for 10-15 minutes per session, twice daily.

Timeline

Start date
2025-08-01
Primary completion
2026-08-31
Completion
2028-08-31
First posted
2025-05-21
Last updated
2025-05-21

Source: ClinicalTrials.gov record NCT06983912. Inclusion in this directory is not an endorsement.