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The feasibility and acceptability of a telerehabilitation intervention on patients undergoing total knee arthroplasty in Iran

The feasibility and acceptability of a telerehabilitation intervention on patients undergoing total knee arthroplasty in Iran

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20231020004
Enrollment
30
Registered
2023-10-20
Start date
2024-05-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Telerehabilitation after total knee arthroplasty Total knee arthroplasty, Telerehabilitation, Feasibility studies, Iran

Interventions

The telerehabilitation for the intervention group includes a 4-week telerehabilitation program using virtual visits through a native mobile application called (Dr. Myco) for Android or a web-based sof
s condition post-surgery and will provide necessary instructions regarding wound care and dietary regimens. The surgeon will also provide prescriptions for medications to be used at home and will info
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
Telerehabilitation,Usual care

Sponsors

AJA University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. No prior history of knee replacement 2. Ability to read and write Persian language 3. Access to and be capable of using a personal smartphone or have access to a companion who can use the smartphone, enabling them to utilize the necessary mobile applications for the research.

Exclusion criteria

Exclusion criteria: 1. Having rheumatoid arthritis or other systematic inflammatory diseases and neurological disorders 2. Having cognitive disorders documented in the medical record 3. Having uncorrectable vision and hearing disorders 4. Participating in any knee rehabilitation program outside of study 5. Any unforeseen complications arising during the intervention that render it impossible to proceed 6. Failure to complete a minimum of 9 out of 12 telerehabilitation sessions for the intervention group (with a minimum attendance rate of 75% for telerehabilitation sessions)

Design outcomes

Primary

MeasureTime frame
Feasibility At the end of the study. To measure the study's feasibility, we will track recruitment and questionnaire completion rates. ,Acceptability At the end of the study. 5-point Likert scale

Secondary

MeasureTime frame
Function in daily living (ADL) Before and after intervention Knee injury and osteoarthritis outcome score (KOOS),Symptoms Before and after intervention Knee injury and osteoarthritis outcome score (KOOS) ,Pain Before and after intervention Knee injury and osteoarthritis outcome score (KOOS),Knee related quality of life (QOL) Before and after intervention Knee injury and osteoarthritis outcome score (KOOS),Patient global assessment Before and after intervention Numeric rating scale ,Walking assistant devices Before and after intervention Type and quantity of walking assistance devices used by the patient,Exercise adherence At the end of the study Self-reporting,Adverse events At the end of the study Self-reporting,Number of Persons Receiving In-person Rehabilitation At the end of study Number of persons

Countries

Iran

Contacts

Public ContactNavvab Farrokhi

Faculty of Rehabilitation, Iran univercity of Medical Sciences

navvabfarrokhi.pt@gmail.com989129536998

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026