Health Condition 1: M238- Other internal derangements of knee
Conditions
Interventions
Intervention1: Virtual Reality Based Rehabilitation: Participants in the intervention group will receive Virtual Reality-based rehabilitation for 70 minutes per session, starting from the first post-o
Sponsors
Justin Jeya Amutha
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults aged 18 to 65 years who have undergone knee related surgeries 2. Medically stable and cleared for participation in postoperative rehabilitation. 3. Intellectual and ability to participate in the study. 4. Who are willing to participate in the study 5. Primary care giver 6. Able to provide informed consent. 7. Able to understand the instructions and engage cognitively in the study. 8. Possess adequate visual and auditory function to interact with VR tools
Exclusion criteria
Exclusion criteria: 1. Patient with open or compound fracture in the Lower extremity. 2. Patient medically restricted to perform exercises 3. Patients having visual and vestibular impairments affecting VR use 4. Severe comorbidities (e.g., Cardiovascular, neurological, psychiatric) impacting participation. 5. Presence of spine fractures that compromise postural control. 6. Major peripheral nerve injuries affecting lower limb function. 7. Currently pregnancy or taking psychotropic medications affecting cognition or balance
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional RecoveryTimepoint: Outcome measures will be assessed at the following time points: baseline on Post-operative Day 1 (prior to initiation of intervention), Day 7 (before discharge), Day 14 (first follow-up visit), and Day 21 (second follow-up visit). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Self efficacy - Self Efficacy for Rehabilitation Outcome Scale 2.constipation -Constipation assessment skill scale 3.Sleep quality-Pittsburgh Sleep Quality Index 4.Satisfaction -User satisfaction Evaluation Questionnaire Timepoint: Outcome measures will be assessed at baseline on Post-operative Day 1 (prior to intervention), & subsequently on Day 7, Day 14, & Day 21. | — |
Countries
India
Contacts
Public ContactJustin Jeya Amutha
Sri Ramachadra Institute of hIgher education and research
Outcome results
None listed