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The Effectiveness of Combined Care for Knee Replacement Patients

NCT06393075 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2024-05-01

No results posted yet for this study

Summary

The goal of this clinical trial is to compare the effectiveness of combined care guidance and general care guidance on pain scores, anxiety levels and joint mobility in patients undergoing total artificial knee replacement. The main questions it aims to answer are:

* Does combined care coaching reduce patient pain scores and anxiety levels after surgery?
* Does combined care guidance improve knee joint mobility after surgery? Researchers will compare combined care guidance and general care to see if combined care guidance reduces patients' pain scores and anxiety levels after surgery, and improves knee joint mobility after surgery.

Participants will:

* Watch pain and rehabilitation exercise guidance videos before surgery and learn how to use a walker.
* Complete questionnaires before surgery, 24 hours, 48 hours, 72 hours and three months after surgery.
* Questionnaire records pain level, anxiety level and joint mobility.

Conditions

  • Arthroplasty, Knee Replacement

Interventions

BEHAVIORAL

combined care guidance

Pain care guidance animation Rehabilitation exercise guidance animation Demonstrate how to perform rehabilitation exercises Demonstrate how to use a walker

BEHAVIORAL

general care guidance

general care guidance

Sponsors & Collaborators

  • Taipei Veterans General Hospital, Taiwan

    lead OTHER_GOV

Principal Investigators

  • LI YING-HUNG, 32 · Employment relationship

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-01
Primary Completion
2024-10-30
Completion
2024-12-30

Countries

  • Taiwan

Study Locations

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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 NCT06393075 on ClinicalTrials.gov