Meniscus; Degeneration Clinical Trial
Official title:
The Effect of Telerehabilitation and Conventional Rehabilitation on Clinical Outcomes and Exercise Compliance in Patients With Degenerative Meniscal Injury
NCT number | NCT05233839 |
Other study ID # | Mugla |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 15, 2022 |
Est. completion date | July 15, 2022 |
Verified date | August 2022 |
Source | Mugla Sitki Koçman University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 49 |
Est. completion date | July 15, 2022 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
Turkey | Mugla Sitki Koçman Training and Research Hospital | Mugla | Mentese |
Lead Sponsor | Collaborator |
---|---|
Mugla Sitki Koçman University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analog Scale (VAS) | On a 10 cm straight line or numerical scale (0: no pain, 10: unbearable pain). | Change from Baseline VAS at 8 weeks | |
Primary | Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) | WOMAC consists of 3 main headings: pain intensity, stiffness, and physical function. The total score ranges from 0 (no disability) to 96 (complete disability). | Change from Baseline WOMAC at 8 weeks | |
Primary | SF-12 | 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. | Change from Baseline SF-12 at 8 weeks | |
Primary | Muscle Strength Test with Lafayette Hand Held Dynamometer | 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. | Change from Baseline Dynamometer Value at 8 weeks | |
Primary | Proprioception Measurement with Baseline Bubble Inclinometer | 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. | Change from Baseline Inclinometer Value at 8 weeks | |
Secondary | EARS | In 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. | Change from Baseline EARS at 8 weeks | |
Secondary | TSUQ | It 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. | Change from Baseline TSUQ at 8 weeks |
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