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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06280365
Other study ID # 012
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 19, 2024
Est. completion date March 15, 2024

Study information

Verified date April 2024
Source Okan University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the effect of the MWM technique on pain, normal joint movement, proprioception and quality of life in patients with knee osteoarthritis (OA).


Description:

The aim of this study is to investigate the effect of the MWM technique on pain, normal joint movement, muscle strength, proprioception, mobility, balance, functionality and quality of life in patients with knee OA.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date March 15, 2024
Est. primary completion date March 15, 2024
Accepts healthy volunteers No
Gender All
Age group 25 Years to 65 Years
Eligibility Inclusion Criteria: - being diagnosed with knee osteoarthritis, - being diagnosed with knee OA at the earliest 6 months ago Exclusion Criteria: - Participants who were pregnant, - had knee surgery, had an infection, - had a pacemaker, had an infraction, - had cancer, or were receiving corticosteroid treatment were excluded from the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mulligan Mobilization with Movement Technique
Mobilization Technique

Locations

Country Name City State
Turkey Emine Atici Tuzla Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Okan University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analog Scale (VAS) VAS, which digitizes parameter values that cannot be measured numerically, was used to evaluate the pain intensity of the participants. The two extreme values of the parameter to be measured are written on the scale as 0 and 10. The person is asked to mark the value that best suits him/her on the scale. For pain, no pain and very severe pain; It is specified as 0 and 10. The person chooses a value according to his/her pain 4 week change in pain intensity
Primary Short form-36 (SF-36) SF-36, developed in 1992, consists of 36 items providing measurement to the following 8 dimensions: physical functioning (10 items), social functioning (2 items), role limitations due to physical problems (4 items), role limitations due to emotional problems (3 items), mental health (5 items), energy/vitality (4 items), pain (2 items), and general health perception (5 items). An increase in the score indicates a higher rate of improvement in health status. 4-week change in quality of life
Primary Western Ontario and Mcmaster Universities Osteoarthritis Index (WOMAC) This survey is conducted to evaluate how much the routine activities in the participants' lives are affected by the knee problem. The survey included the following parameters: pain, physical function, and stiffness. A Likert system ranging from 1 to 5 is used. As the value increases, the intensity of the parameters increases 4-week
Primary Evaluation of proprioception To assess the participants' sense of proprioception, the method of actively reproducing the passive position without supporting the limb was used. In this assessment, where the angle is measured with a goniometer, the person closes their eyes. The limb is passively moved to the target angle and the person is asked to concentrate on the position. After 10 seconds, the starting point of the movement is returned. The person tries to find the target angle by actively moving the same limb. If the angle achieved at the end of the movement is different from the target angle, the difference is recorded as the deviation angle (used to 15° and 45° knee flexion). 4-week change in proprioception
Primary The range of motion A goniometer (Baseline plastic goniometer), which provides numerical and objective results, was used to measure the range of motion of the participants. Knee flexion for normal range of motion in the knee region and knee extension angles were evaluated. 4-week
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