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Clinical Trials/NCT05233839
NCT05233839
Completed
N/A

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

Muğla Sıtkı Koçman University1 site in 1 country49 target enrollmentMarch 15, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Meniscus; Degeneration
Sponsor
Muğla Sıtkı Koçman University
Enrollment
49
Locations
1
Primary Endpoint
Visual Analog Scale (VAS)
Status
Completed
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 15, 2022
End Date
July 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Muğla Sıtkı Koçman University
Responsible Party
Principal Investigator
Principal Investigator

Fatih Ozden

Principal Investigator

Muğla Sıtkı Koçman University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Visual Analog Scale (VAS)

Time Frame: Change from Baseline VAS at 8 weeks

On a 10 cm straight line or numerical scale (0: no pain, 10: unbearable pain).

Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

Time Frame: Change from Baseline WOMAC at 8 weeks

WOMAC consists of 3 main headings: pain intensity, stiffness, and physical function. The total score ranges from 0 (no disability) to 96 (complete disability).

SF-12

Time Frame: Change from Baseline SF-12 at 8 weeks

SF 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.

Muscle Strength Test with Lafayette Hand Held Dynamometer

Time Frame: Change from Baseline Dynamometer Value at 8 weeks

It 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 Inclinometer

Time Frame: Change from Baseline Inclinometer Value at 8 weeks

The "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.

Secondary Outcomes

  • EARS(Change from Baseline EARS at 8 weeks)
  • TSUQ(Change from Baseline TSUQ at 8 weeks)

Study Sites (1)

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