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Comparison of Telerehabilitation vs Clinical Setup Rehabilitation in TKR Patients

S

Superior University

Status

Active, not recruiting

Conditions

Knee Injuries

Treatments

Other: Traditional Physical Preatment
Behavioral: Conventional Physiotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06457620
MSRSW/Batch-Fall22/725

Details and patient eligibility

About

This study examines the feasibility, attainability, and patient satisfaction of telerehabilitation and clinical consultation rehabilitation.

Full description

The objective is to assess whether telerehabilitation can provide comparable or significantly better outcomes in terms of functional recovery, pain management, improved range of motion, and patient satisfaction for Total Knee Replacement (TKR) patients. If telehealth interventions prove successful, they can be implemented to increase access to high-quality rehabilitation treatments and enhance healthcare delivery. Evidence-based findings from this study can help healthcare providers make educated decisions about incorporating telerehabilitation into post-operative rehabilitation protocols, thereby enhancing patient care and optimizing resource utilization in orthopedic settings.

Enrollment

36 patients

Sex

All

Ages

65 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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)

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

conventional physiotherapy
Experimental group
Treatment:
Behavioral: Conventional Physiotherapy
traditional physical treatment
Other group
Treatment:
Other: Traditional Physical Preatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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