NCT06901661

Brief Summary

Digital health utilization in the form of telerehabilitation is a popular technology that is very little researched for musculoskeletal disorders particularly hip and knee osteoarthritis (OA). The progression of OA will lead to total hip or knee replacement surgery. As a consequence, the advancing aging population leads to an increased burden on the healthcare system due to rising osteoarthritis. That's why, we will conduct a randomized controlled trial to explore the effectiveness of telerehabilitation in hip and knee osteoarthritis. This study will recruit OA patients into control and experimental groups. The control group will receive a patient education while the experimental group will undergo remote exercise sessions. Both groups will receive one supervised session a week for 5 weeks. The pre- and post-outcome measures will be recorded for functional status of hip and knee, muscle strength, and range of motions of the lower extremity. This innovative study will evaluate the effectiveness of a telemedicine intervention applied to a clinical population in Taiwan. The use of telerehabilitation interventions aims to reduce treatment and transportation costs, as well as save time for patients with OA. This digital health approach also helps to alleviate the workload of physiotherapists and rehabilitation doctors in clinics. The findings from this study could broaden the scope for using remote digital technology to assist clinical patients in diverse settings, especially those with limited or no hospital access.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial recruitment is currently suspended
Enrollment
110

participants targeted

Target at P50-P75 for not_applicable

Timeline
6mo left

Started Aug 2025

Geographic Reach
1 country

1 active site

Status
suspended

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress65%
Aug 2025Dec 2026

First Submitted

Initial submission to the registry

March 23, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 30, 2025

Completed
4 months until next milestone

Study Start

First participant enrolled

August 6, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 26, 2025

Completed
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Expected
Last Updated

May 5, 2026

Status Verified

April 1, 2026

Enrollment Period

5 months

First QC Date

March 23, 2025

Last Update Submit

April 29, 2026

Conditions

Keywords

TelerehabilitationOsteoarthritisRandomized controlled trial

Outcome Measures

Primary Outcomes (1)

  • Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

    A questionnaire

    The outcome measures will be recorded before and after finish all 5 week of the intervention

Secondary Outcomes (2)

  • Muscle strength

    The outcome measures will be recorded before and after finish all 5 week of the intervention

  • Range of motion

    The outcome measures will be recorded before and after finish all 5 week of the intervention

Other Outcomes (2)

  • Borg rate of perceived exertion (RPE)

    Evaluate every week for 5 weeks during each exercise session of the experimental group

  • International Physical Activity Questionnaire-Short Form (IPAQ-SF)

    The outcome measures will be recorded before and after finish all 5 week of the intervention

Study Arms (2)

Telerehabilitation

EXPERIMENTAL

Receive a remote exercise program for 40 minutes once a week for 5 weeks

Behavioral: Telerehabilitation

Standard care

PLACEBO COMPARATOR

Receive a patient education session once a week for 5 weeks

Behavioral: Standard care

Interventions

Exercise program include Warm-up, Targeted muscle Strengthening, Joint mobilization, and Proprioception

Telerehabilitation
Standard careBEHAVIORAL

Education session on their pain, disability, and functional activities

Standard care

Eligibility Criteria

Age35 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • diagnosed with hip or knee osteoarthritis within last one year
  • having sub-acute or chronic symptoms of pain and functional disability
  • living in an area served by high-speed Internet services (at least 512 kb/s in upload)
  • living within an hour driving distance from the treating hospital
  • physically fit to provide a written consent to participate in this study

You may not qualify if:

  • taking sedatives, autoimmune, or other medication that can interfere with their exercise program
  • any health issues that could affect the tests or the rehabilitation program, including surgery over the recent six months
  • having diagnosed with cognitive disorders
  • having recent surgery or major postoperative complications

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taipei Medical University-Shuang Ho Hospital, Ministry of Health and Welfare

New Taipei City, 235, Taiwan

Location

MeSH Terms

Conditions

Osteoarthritis, KneeOsteoarthritis, HipOsteoarthritis

Interventions

TelerehabilitationStandard of Care

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Intervention Hierarchy (Ancestors)

RehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and ServicesTelemedicineDelivery of Health CarePatient Care ManagementHealth Services AdministrationQuality Indicators, Health CareQuality of Health CareHealth Care Quality, Access, and Evaluation

Study Officials

  • Hung-Chou Chen, Dr.

    Taipei Medical University Shuang Ho Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 23, 2025

First Posted

March 30, 2025

Study Start

August 6, 2025

Primary Completion

December 26, 2025

Study Completion (Estimated)

December 1, 2026

Last Updated

May 5, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations