Comparison of Telerehabilitation vs Clinical Setup Rehabilitation in TKR Patients
1 other identifier
interventional
36
1 country
1
Brief Summary
This study examines the feasibility, attainability, and patient satisfaction of telerehabilitation and clinical consultation rehabilitation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2024
CompletedFirst Submitted
Initial submission to the registry
June 10, 2024
CompletedFirst Posted
Study publicly available on registry
June 13, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
October 30, 2024
CompletedJune 13, 2024
June 1, 2024
6 months
June 10, 2024
June 10, 2024
Conditions
Outcome Measures
Primary Outcomes (2)
Western Ontario and McMaster Universities Osteoarthritis (WoMAC)
The WOMAC consists of three subscales: pain (five questions), stiffness (two questions), and physical function (17 questions). The subscale scores can vary, with pain ranging from 0 to 20 points; stiffness, 0 to 8 points; and physical function, 0 to 68 points. ,
12 Months
Knee Outcome Survey-Activities of Daily Living (KOS-ADLS)
The Knee Outcome Survey (KOS) is a patient-completed questionnaire that provides a percentage of disability during every day activities (activities of daily living subscale) or sports (sports activity subscale). The lower the percentage, the higher the disability.
12 months
Study Arms (2)
conventional physiotherapy
EXPERIMENTALtraditional physical treatment
OTHERInterventions
Each participant received conventional physiotherapy at the clinic as a part of their management plan. Group A exercise was five times a week for thirty minutes, beginning on the third day after total knee arthroplasty (TKA). The program aimed to improve leg strength, core stability, balance, and overall performance through exercise instructions. The baseline evaluation was completed one day before the TKA, and the posttest was completed four weeks after the TKA.
Each participant got traditional physical treatment during a video conference as part of telerehabilitation. The physiotherapy assistant contacted Group B to arrange a virtual follow-up clinic appointment via Zoom or WhatsApp, along with a 4-week program. We inquired about the patient's level of satisfaction with their TKR procedure. The patient was informed that clinical photos were taken, and the video call was to be recorded. Before the virtual clinic, each patient's verbal agreement was acquired. With workout instructions, the program pursued to enhance leg strength, core stability, balance, and overall performance. The posttest was conducted four weeks after the TKA, and the baseline assessment was finished one day before the procedure.
Eligibility Criteria
You may qualify if:
- Male and female patients diagnosed with TKR
- Older Age above 65
- Patient communicates with medical staff
- Patient with cemented TKA
- Patients who underwent TKA owing to degenerative arthritis
You may not qualify if:
- Older patients aged \>75 years
- Patient with a history of knee joint surgery before TKA
- Patient who possibly had a systematic inflammatory disease such as rheumatoid arthritis.
- Patients with difficulty in seeing, hearing, and walking independently
- Patients having a history of mental illnesses (Stroke, Multiple sclerosis, Parkinsonism, Alzheimer's Disease)
- Patient history of severe mobility disorder
- Systemic illness (Liver Failure, Active cancer, Cardiopulmonary distress)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Acti Life Physiotherapy and Rehabilitation Center Horizon Hospital
Lahore, Punjab Province, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 10, 2024
First Posted
June 13, 2024
Study Start
November 1, 2023
Primary Completion
May 1, 2024
Study Completion
October 30, 2024
Last Updated
June 13, 2024
Record last verified: 2024-06
Data Sharing
- IPD Sharing
- Will not share