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Efficacy of Telerehabilitation in Patients With Degenerative Meniscal Injury

The Effect of Telerehabilitation and Conventional Rehabilitation on Clinical Outcomes and Exercise Compliance in Patients With Degenerative Meniscal Injury

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05233839
Enrollment
49
Registered
2022-02-10
Start date
2022-03-15
Completion date
2022-07-15
Last updated
2022-09-01

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

Conditions

Meniscus; Degeneration

Keywords

Degenerative meniscus injury, Telerehabilitation

Brief summary

The aim of the study is to compare the home exercise program performed with video-based telerehabilitation in patients with degenerative meniscal injury, and the home exercise program performed with one-on-one training in the hospital with conventional methods.

Detailed description

Conventional rehabilitation (CR) practices will be applied to the first study group. Telerehabilitation (TR) application will be applied to the second study group. It is aimed to evaluate the patients in terms of pain, functionality, quality of life and exercise compliance.

Interventions

OTHERTelerehabilitation

Application based video home exercise for the degenerative meniscus injury

Paper instruction based home exercise for the degenerative meniscus injury

Sponsors

Muğla Sıtkı Koçman University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomised controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male and female patients aged 18 - 65 years * Having been diagnosed with degenerative meniscus injury by an orthopedist by MRI examination * Having signed the consent form

Exclusion criteria

* Situations that will prevent assessments or communication with the individual * Having an operation due to degenerative meniscus injury problem * Orthopedic and neurological problems that would prevent evaluation and/or treatment

Design outcomes

Primary

MeasureTime frameDescription
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)Change from Baseline WOMAC at 8 weeksWOMAC consists of 3 main headings: pain intensity, stiffness, and physical function. The total score ranges from 0 (no disability) to 96 (complete disability).
Muscle Strength Test with Lafayette Hand Held DynamometerChange from Baseline Dynamometer Value at 8 weeksIt is an objective muscle strength measurement tool. Measurements are made 3 times. A rest of 120 seconds is given between measurements. The highest measured value is noted.
Proprioception Measurement with Baseline Bubble InclinometerChange from Baseline Inclinometer Value at 8 weeksThe absolute angle difference, which is the difference between the targeted angle and the angle realized by the patient in each repetition, is recorded. The arithmetic mean of the absolute angle difference of 3 repetitions is the result data.
Visual Analog Scale (VAS)Change from Baseline VAS at 8 weeksOn a 10 cm straight line or numerical scale (0: no pain, 10: unbearable pain).
SF-12Change from Baseline SF-12 at 8 weeksSF 12 is a self-evaluation scale. It consists of seven items. Its score ranged from 0 to 100, with higher scores indicating better physical and mental health functioning.

Secondary

MeasureTime frameDescription
TSUQChange from Baseline TSUQ at 8 weeksIt consists of 21 items. With this survey, the satisfaction levels and usability of individuals using the telemedicine service are evaluated. The total score is scored between 17 and 85. Higher scores indicate higher satisfaction and usability.
EARSChange from Baseline EARS at 8 weeksIn order to observe the individual's adaptation to exercise, the motivation levels of the patients regarding the exercise program are evaluated with the exercise diary prepared by the researchers of the study. It is scored between 0 to 24. Higher scores indicate greater adherence.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026