TerminatedNot Applicable

VR-Based Preoperative Rehabilitation Program for Patients Undergoing Anterior Cruciate Ligament (ACL) Reconstruction

Stopped: The sample size is insufficient

China100 participantsStarted 2024-04-02

Plain-language summary

Between April 2, 2024, and October 1, 2024, a study will be conducted at the Department of Orthopedics in the First Affiliated Hospital of Shantou University Medical College involving 120 patients who will undergo anterior cruciate ligament reconstruction surgery. They will be randomly divided into two groups: an experimental group and a control group.

Who can participate

Age range18 Years – 60 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Individuals eligible for inclusion in the study are those who undergo their initial anterior cruciate ligament (ACL) reconstruction surgery, aged between 18 and 60 years, possess adequate hearing and vision, have clear consciousness, and demonstrate proficient language communication skills. Exclusion Criteria: * Individuals with cognitive impairments, severe hearing or vision impairments, limb paralysis, or non-compliance with the experiment will be excluded from participation.

What they're measuring

knee joint range of motion

Timeframe: through study completion, an average of 6 months

Lysholm knee function score

Timeframe: through study completion, an average of 6 months

Trial details

NCT IDNCT06347523

SponsorFirst Affiliated Hospital of Shantou University Medical College

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-03-01

View on ClinicalTrials.gov More Anterior Cruciate Ligament (ACL) Reconstruction trials