Effects of Action Observation Therapy on Pain, Functional Level and Brain Hemodynamic in Patients With Knee Osteoarthritis

Overview

In this project, investigators aim to investigate the effects of action observation therapy on pain, fear of movement, functional level and brain hemodynamics in patients with knee osteoarthritis. The study is unique in that this method, which has already been used for post-surgical or motor healing, aims at long-term administration for the first time with chronic pain and objective visualization of the results. This study will create a new perspective to understand the physiology of pain, which has attracted much interest in the literature in recent years, and will shed light on the studies that can be done in this regard. Participants' joint range of motion in the initial assessments will be measured by electro-goniometer, muscle strength assessment by JTech hand dynamometer at appropriate evaluation positions. In assessing pain, pain levels at rest and during activity will be questioned using Visual Analog Scale. Fear of movement of individuals will be assessed via Tampa Kinesiophobia Scale and functional levels will be assessed via Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and the Timed Up and Go Test. Functional near infrared spectroscopy (fNIRS) will be used for evaluation of brain hemodynamics. The first group, will receive exercises with action observation therapy; and the second group will receive only exercises. The exercise programme will be administered under physiotherapist supervision for three days a week for six weeks. The evaluations will be repeated at the beginning of the study and at the end of the sixth week. Data obtained from the study will be analyzed using appropriate statistical methods.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: Double (Participant, Outcomes Assessor)
  • Study Primary Completion Date: May 15, 2019

Detailed Description

Osteoarthritis is a degenerative joint disease associated with pain and disability that occurs in 25% of the population over 18 years of age Worldwide. It is expected that osteoarthritis will be the fourth most common cause of disability in the World by 2020. Osteoarthritic joint has pathological changes such as damage of joint cartilage tissue, thickening of the subchondral bone, osteophyte formation, inflammation of synovium at different levels, degeneration of ligaments and meniscal structures and hypertrophy of joint capsule. In recent years, studies that relate chronic pain to neuroplasticity have demonstrated changes in the structure, function and somatotopic organization of the primary motor and sensory cortex of osteoarthritis patients with chronic pain. In addition to this, osteoarthritis studies showed that the pain does not originate solely from joint problems; the central nervous system is also responsible for the formation of pain sensation. Changes in the cortical sensorimotor areas include sensory disturbances, perceptual problems (differentiation of body image), and motor influences, and these changes are associated with severity and duration of pain. When the central nervous system targeted, pain may decrease better. Action observation therapy is a method which activates mirror neurons. In this project, investigators aim to investigate the effects of action observation therapy on pain, fear of movement, functional level and brain hemodynamics in patients with knee osteoarthritis. The study is unique in that this method, which has already been used for post-surgical or motor healing, aims at long-term administration for the first time with chronic pain and objective visualization of the results. This study will create a new perspective to understand the physiology of pain, which has attracted much interest in the literature in recent years, and will shed light on the studies that can be done in this regard.

Interventions

  • Other: Action observation therapy
    • The normal human movement will be recorded and than the patients will be watched them.
  • Other: Exercise
    • Strengthening and stretching exercise programme focuses on hip and knee muscles

Arms, Groups and Cohorts

  • Active Comparator: Exercise
    • Strengthening and stretching exercises for hip and knee muscles, balance and proprioceptive exercises
  • Experimental: Action observation therapy and exercise
    • Video of normal human movement and Strengthening and stretching exercises for hip and knee muscles

Clinical Trial Outcome Measures

Primary Measures

  • Brain Hemodynamics
    • Time Frame: 6 weeks
    • Functional near infrared spectroscopy will be used to assess the brain hemodynamics during the observation of actions, motor imagery and active movement.
  • Pressure pain threshold
    • Time Frame: 6 weeks
    • Algometer (dolorimeter) will be used to assess the pressure pain threshold.
  • Visual Analog Scale
    • Time Frame: 6 weeks
    • Self reported pain intensity during rest and walking measured by 0-10 point scale.

Participating in This Clinical Trial

Inclusion Criteria

  • Between 45 to 70 years; – Unilateral knee osteoarthritis according to clinical and radiological criteria – Grade 2 or Grade 3 according to Kellgren-Lawrance Scale – Right-handed according to Edinburgh Handedness Scale – Chronic pain during the rest or activity above 4 points according to the Verbal Rating Scale Exclusion Criteria:

  • Having neurological or psychiatric diseases – Having chronic pain due to another pain disorder – Having rheumatic diseases – Using antidepressant medications or opioids – Knee surgery within one year prior to the study – Intraarticular injection and attend physical therapy within 6 months prior to the study – Mini Mental State Examination Scale score below 24

Gender Eligibility: All

Minimum Age: 45 Years

Maximum Age: 70 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Acibadem University
  • Provider of Information About this Clinical Study
    • Principal Investigator: Özgül Öztürk, Doctor – Acibadem University

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