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Clinical Trials/NCT05767788
NCT05767788Active, not recruitingNot Applicable

Effectiveness of Mobilization With Movement (MWM) on Patients With Knee Osteoarthritis (OA): A Double-blinded Randomized Sham-controlled Trial

The Hong Kong Polytechnic University1 site in 1 country40 target enrollmentStarted: December 10, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
40
Locations
1
Primary Endpoint
Change of pain in the Visual Analogue Scale (VAS)

Study Overview

Brief Summary

Movement with mobilization (MWM) is an effective manual therapy to improve pain and function of patients with knee osteoarthritis (OA).

However, immediate, and prolonged effects after prolonged MWM period was under-investigated.

In this double-blinded randomized control trial, 40 patients are needed. The subjects and assessors will be blinded. Subjects in intervention group will receive MWM twice a week and corresponding home exercise for 6 weeks.

Participants in control group will only receive sham treatment with light touch.

The effects on knee pain in visual analogue scale (VAS); flexion and extension range of motion (ROM) by goniometer; strength by hand-held dynamometer; function by Timed Up and Go Test (TUG) and 30-second Chair Stand Test; and health-related quality of life (HRQoL) by Knee Injury and Osteoarthritis Outcome Score (KOOS) and Western Ontario and McMaster Universities Arthritis Index (WOMAC) just after, 1-month and 3-month after treatment will be compared with baseline. Six-month after treatment, KOOS and WOMAC will be conducted.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
40 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •History of knee OA for at least 1-year
  • •Pain intensity level ≥ 3 on a 10-cm Visual Analogue Scale (VAS)
  • •Both unilateral or bilateral knee pain
  • •Having morning stiffness less than 30 minutes
  • •Having crepitus on active movement
  • •Having bony tenderness
  • •Having bony enlargement

Exclusion Criteria

  • •Having active inflammatory or infectious knee conditions
  • •Having bone integrity conditions like osteoporosis
  • •Having knee joint instability
  • •Having skin integrity conditions like frail skin or lower limb peripheral vascular disease
  • •History of hip or knee fracture
  • •History of knee surgical history
  • •Use of knee corticosteroid or opioid injection

Arms & Interventions

Movement with Mobilization (MWM)

Experimental

Active movement with passive mobilization gliding force

Intervention: Movement with Mobilization (MWM) (Other)

Sham Movement with Mobilization (Sham MWM)

Sham Comparator

Active movement with passive light touch gliding force

Intervention: Sham Movement with Mobilization (Sham MWM) (Other)

Outcomes

Primary Outcomes

Change of pain in the Visual Analogue Scale (VAS)

Time Frame: The change before the start of treatment and 3-month after last treatment session

Subjects will indicate the pain level on a 100-millimeter line with endpoints, marked "no pain" and "worst imaginable pain", at the time of assessment.

Change of pain in the Visual Analogue Scale (VAS)

Time Frame: The change before the start of treatment and after 6-week treatment

Subjects will indicate the pain level on a 100-millimeter line with endpoints, marked "no pain" and "worst imaginable pain", at the time of assessment.

Change of pain in the Visual Analogue Scale (VAS)

Time Frame: The change before the start of treatment and 1-month after last treatment session

Subjects will indicate the pain level on a 100-millimeter line with endpoints, marked "no pain" and "worst imaginable pain", at the time of assessment.

Secondary Outcomes

  • Change of time used in the Timed Up and Go Test (TUG)(The change before the start of treatment and 3-month after last treatment session)
  • Change of number of repetitions in the 30-second Chair Stand Test (30CST)(The change before the start of treatment and 3-month after last treatment session)
  • Change of knee flexors muscle strength by the hand-held dynamometer(The change before the start of treatment and 3-month after last treatment session)
  • Change of knee extensors muscle strength by the hand-held dynamometer(The change before the start of treatment and 3-month after last treatment session)
  • Change of score of the Knee Injury and Osteoarthritis Outcome Score (KOOS)(The change before the start of treatment and 6-month after last treatment session)
  • Change of score of the Western Ontario and McMaster Universities Arthritis Index (WOMAC)(The change before the start of treatment and 6-month after last treatment session)
  • Change of active knee flexion range of motion by the standard goniometer(The change before the start of treatment and 3-month after last treatment session)
  • Change of active knee extension range of motion by the standard goniometer(The change before the start of treatment and 3-month after last treatment session)
  • Change of time used in the Timed Up and Go Test (TUG)(The change before the start of treatment and after 6-week treatment)
  • Change of time used in the Timed Up and Go Test (TUG)(The change before the start of treatment and 1-month after last treatment session)
  • Change of number of repetitions in the 30-second Chair Stand Test (30CST)(The change before the start of treatment and after 6-week treatment)
  • Change of number of repetitions in the 30-second Chair Stand Test (30CST)(The change before the start of treatment and 1-month after last treatment session)
  • Change of knee flexors muscle strength by the hand-held dynamometer(The change before the start of treatment and after 6-week treatment)
  • Change of knee flexors muscle strength by the hand-held dynamometer(The change before the start of treatment and 1-month after last treatment session)
  • Change of knee extensors muscle strength by the hand-held dynamometer(The change before the start of treatment and after 6-week treatment)
  • Change of knee extensors muscle strength by the hand-held dynamometer(The change before the start of treatment and 1-month after last treatment session)
  • Change of score of the Knee Injury and Osteoarthritis Outcome Score (KOOS)(The change before the start of treatment and after 6-week treatment)
  • Change of score of the Knee Injury and Osteoarthritis Outcome Score (KOOS)(The change before the start of treatment and 1-month after last treatment session)
  • Change of score of the Knee Injury and Osteoarthritis Outcome Score (KOOS)(The change before the start of treatment and 3-month after last treatment session)
  • Change of score of the Western Ontario and McMaster Universities Arthritis Index (WOMAC)(The change before the start of treatment and after 6-week treatment)
  • Change of score of the Western Ontario and McMaster Universities Arthritis Index (WOMAC)(The change before the start of treatment and 1-month after last treatment session)
  • Change of score of the Western Ontario and McMaster Universities Arthritis Index (WOMAC)(The change before the start of treatment and 3-month after last treatment session)
  • Change of active knee flexion range of motion by the standard goniometer(The change before the start of treatment and after 6-week treatment)
  • Change of active knee flexion range of motion by the standard goniometer(The change before the start of treatment and 1-month after last treatment session)
  • Change of active knee extension range of motion by the standard goniometer(The change before the start of treatment and after 6-week treatment)
  • Change of active knee extension range of motion by the standard goniometer(The change before the start of treatment and 1-month after last treatment session)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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