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临床试验/CTRI/2026/01/102429
CTRI/2026/01/102429尚未招募4 期

Effect of Graded Motor Imagery for Enhanced Recovery in rehabilitation of individuals after Anterior Cruciate Ligament Reconstruction on Pain, Mobility, Kinesiophobia, Mental imagery ability and Functions: A Randomized Controlled Trial

未提供1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2027年2月11日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
72
试验地点
1
主要终点
Pain, Range of motion, Kinesiophobia, Motor imagery ability, Functions

研究概览

简要总结

Individuals diagnosed with ACL injury and scheduled for reconstructive surgeries will be screened for eligibility using inclusion and exclusion criteria**.** The study procedures will be explained to the participants and informed consent will be obtained. The demographic data and all the baseline outcome measures will be assessed. All the participants will then be divided into two groups usingcomputer-generated randomization sequence number table. The intervention group will receive Graded motor imagery in addition to the traditional rehabilitation (GMI: 2 week preoperative, perioperative and 3 week postoperative plus Traditional rehabilitation: 2 week preoperative, 3 peek post operative and home exercise program till 3 month follow up)whereas group B will only receive Standard Rehabilitation Traditional rehabilitation: 2 week preoperative, 3 peek post operative and home exercise program till 3 month follow up) The outcome measures will be assessed at 3 timeframes. Baseline;  At 5 week (3week post op) and ; 3 month follow up. The home exercise program will be monitored by Telephonic follow up and home diary. Any adverse events will be managed by qualified personnel, and appropriate care will be provided if required

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • All gender Aged 18-
  • Individuals with a confirmed diagnosis of Grade 2 or Grade 3 ACL tear on MRI and who are scheduled for reconstructive surgery.
  • Individuals who opted for Spinal anesthesia during the surgical procedure.
  • Able to follow verbal instructions and cognitively engage with imagery techniques (Clinician judgment).

排除标准

  • Not willing to participate
  • Visual or cognitive impairments that preclude engagement in GMI tasks
  • Non-compliance with rehab protocols or inability to attend follow-up sessions
  • Uncontrolled systemic illness or comorbidities (e.g., uncontrolled diabetes, severe cardiac or respiratory disease)
  • Severe psychiatric illness (e.g., psychosis, major depression) that may interfere with participation
  • History of previous lower limb injury/ trauma.

结局指标

主要结局

Pain, Range of motion, Kinesiophobia, Motor imagery ability, Functions

时间窗: at baseline 3 weeks 3 months

次要结局

  • Quadriceps & Hamstring Strength,Postural Stability, Length of Hospital Stay, Patient Satisfaction(at baseline 3 weeks 3 months)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Rutuja Phadke

Bharati Vidyapeeth (Deemed to University)

研究点 (1)

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