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Completed

NCT Number: NCT06280365

MWM Technique in Patients With Knee OA

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).

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Key information

Age range

25 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Emine Atıcı

Tuzla, Istanbul, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Mulligan mobilization with movement technique

Other

Mobilization Technique

Primary outcomes

  1. Visual Analog Scale (VAS)

    Time frame: 4 week change in pain intensity

    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

  2. Short form-36 (SF-36)

    Time frame: 4-week change in quality of life

    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.

  3. Western Ontario and Mcmaster Universities Osteoarthritis Index (WOMAC)

    Time frame: 4-week

    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. Evaluation of proprioception

    Time frame: 4-week change in 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).

  5. The range of motion

    Time frame: 4-week

    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.

Sponsors and collaborators

Lead sponsor

Okan University

Other

Registry information

Official study title

Effects of Mulligan Mobilization With Movement (MWM) Technique in Patients With Knee Osteoarthritis

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Feb 28, 2024
Registry last updated
Aug 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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