跳至主要内容
临床试验/CTRI/2025/01/079542
CTRI/2025/01/079542尚未招募不适用

Evaluation of effectiveness of mobile based application versus conventional follow up training for the post operative rehabilitation in ACL reconstruction patients

Dr Ramprasath Rajavel1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年2月10日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Range of Motion (ROM) of the knee.

研究概览

简要总结

The mobile application for post-operative rehabilitation after ACL reconstruction surgery aims to enhance the recovery process and outcomes for patients undergoing this procedure. Through a user-friendly platform, the app guides patients through their rehabilitation exercises, tracks their progress, and educates them about the post-operative recovery journey. Furthermore, it fosters communication between patients and healthcare providers, facilitating timely support and guidance.Overall, the app seeks to improve patient engagement and adherence to rehabilitation protocols, ultimately leading to better recovery outcomes and overall satisfaction with the treatment process

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 18-65 years who have recently undergone ACL reconstruction surgery (within 1-3 weeks post-surgery), possess access to a smartphone or tablet, and are capable of using mobile applications are eligible for the study.
  • They must be willing to provide informed consent and be proficient in the language of the study materials.

排除标准

  • Participants will be excluded if they are under 18 or over 60 years old, have not undergone ACL reconstruction surgery, or have other significant knee pathologies (e.g., severe osteoarthritis).
  • Exclusion also applies to individuals with severe medical conditions (e.g., uncontrolled diabetes, cardiovascular diseases), mental health impairments, pregnancy, post-surgical complications, inability to use the app, non-adherence risk, or enrollment in other studies.

结局指标

主要结局

Range of Motion (ROM) of the knee.

时间窗: Baseline (prior to intervention initiation, 1-3 weeks post-surgery). | 4 weeks after starting rehabilitation. | 8 weeks after starting rehabilitation. | 16 weeks after starting rehabilitation (end of intervention). | strength, and mobility, as measured by validated clinical scales over the study period

Pain intensity using a Visual Analog Scale (VAS).

时间窗: Baseline (prior to intervention initiation, 1-3 weeks post-surgery). | 4 weeks after starting rehabilitation. | 8 weeks after starting rehabilitation. | 16 weeks after starting rehabilitation (end of intervention). | strength, and mobility, as measured by validated clinical scales over the study period

Functional scores (e.g., Lysholm Knee Scoring Scale or International Knee Documentation Committee [IKDC] score).

时间窗: Baseline (prior to intervention initiation, 1-3 weeks post-surgery). | 4 weeks after starting rehabilitation. | 8 weeks after starting rehabilitation. | 16 weeks after starting rehabilitation (end of intervention). | strength, and mobility, as measured by validated clinical scales over the study period

次要结局

  • Improved rehabilitation adherence rates(assessed through engagement metrics in the)

研究者

发起方
Dr Ramprasath Rajavel
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Ramprasath Rajavel

SAVEETHA MEDICAL COLLEGE AND HOSPITALS

研究点 (1)

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