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CompletedNCT04107350Updated Sep 30, 2019

The Whole Body Vibration Training for Total Knee arthroplasty-the Improvement of the Lower Limb

An interventional study of whole-body vibration in Knee Osteoarthritis, Arthroplasty Complications and Swelling; Leg, sponsored by Kaohsiung Medical University Chung-Ho Memorial Hospital. Completed at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2019-09-30.

Sponsored by Kaohsiung Medical University Chung-Ho Memorial Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Mar 2018, registered Sep 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
20 Years and older
Sex
All
01

Study summary

Knee Osteoarthritis in elder cause pain and decrease their functional activity. After conservative rehabilitation failure, they might receive total knee arthroplasty. The post-operation rehabilitation could improve range of motion and might help them to back activities of daily Living earlier. However, the pain and swelling after the operation of total knee arthroplasty cause the limitation of early mobilization, cause ROM limitation, muscle strength decrease, functional activity decrease, and impaired activity of daily life. In recent studies, the effect of whole body vibration included improving pain, swelling, muscle strength, balance, and functional activity, increasing metabolic rate and decreasing lactate accumulation. the investigators expect the early intervention of whole body vibration and traditional physical therapy on the post-TKA patient could improve ROM, decrease swelling, increased muscle strength, functional activity, and balance as compared with traditional physical therapy.

Read the detailed description
  1. Name: whole body vibration BW-750
  2. Dosage form: frequency 4-10 Hz, 10-15minutes with rest for 3-5 minutes * 2 days in standing position
  3. Dose(s): post-op day2, WBV 4-10 Hz, 10-15minutes with rest for 3-5 minutes, post-op day3 WBV 4-10 Hz, 10-15 minutes with 3-5 minutes in standing position
  4. Dosing schedule: whole body vibration 4-10 Hz for 10-15 minutes with rest 3-5 minutes on post-op day 2 and day3
  5. Mechanism of action: passive muscle contraction, improve swelling, increase blood flow, and improve muscle strength
  6. Pharmacological category: N/A

IV.Study design 1. ■ Control: ■ placebo 2. Blinding: ■ double blind 3. Randomized: ■ yes □ no 4. ■ Parallel 5. Duration of study:from IRB approval \~to 31 , Dec. , 2019 6. Number of subjects: 52 persons 7. Is there any of the followings included DSMB, Data Safety Monitoring Board:

  • no V.Assessment criteria 1. Efficacy: pain (VAS),swelling circumference,knee range of motion,knee extensor muscle strength,time up and go,and Activities of Daily Living 2. Safety: The duration and frequency of whole body vibration is relative low. The risk of damage is very low 3. Pharmacokinetics: Not apply 4. Quality of life: Through facilitate muscle contraction, improve blood flow, and decrease pain could improve muscle power, increase range of motion and ADL VI. Selection criteria

    1. Main inclusion criteria: knee osteoarthritis, post-operation of total knee arthroplasty, single leg
    2. Main exclusion criteria: vital signs unstable, uncontrolled blood pressure, diabetes mellitus, neoplasm, neurological disorder, fibromyalgia, cardiac pacemaker, bilateral TKA, musculoskeletal involvement other than TKA VII.Study procedures(summary)

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    1. Written informed consent must be obtained before any study specific procedures are undertaken.
    2. The process of the experiment (brief describe)

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    1. Randomized distribute participants into two groups, "whole body vibration(experimental group)+ traditional physical therapy" group and "placebo group with traditional physical therapy+ whole body vibration (placebo without turn-on vibration)".
    2. Post-TKA day 1 (not op day) Pre-test (baselin data) include pain(VAS), leg circumference, knee ROM, knee extensor strength (JAMMAR), sit to stand average duration, 6 meters ambulatory test.

      Both groups receive traditional physical therapy and passive continuous passive motion (CPM).

    3. Post-TKA day 2 Both groups keep traditional physical therapy and CPM.

    (1) The experimental group perform pre-test before the treatment. After the pre-test, participants receive 10-15 minutes WBV exercise in standing position, amplitude 2mm, frequency 4-10Hz, with rest about 3-5minutes. After the treatment, perform post-treatment test 1.

    (2) The control group standing on the WBV machine without turn-on for 10-15 minutes and then post-treatment test 1.

    1. Post-TKA day 3
    2. The experimental group participants receive 10-15 minutes WBV exercise in standing position, amplitude 2mm, frequency 4-10 Hz, with rest about 3-5minutes. After the treatment, perform post-treatment test 2.
    3. The control group standing on the WBV machine without turn-on for 10-15 minutes and then post-treatment test 1.

      Statistical analysis 1. Statistical Method for Efficacy / Safety measurements: Demographic data were collected on age, pre-TKA Osteoarthritis X-ray Kellgren-Lawrence classification, sex, weight, height, side of involvement. The investigators use t-test, or chi-square test to confirm homogeneity.

      On the other side, measurement the circulation of the affected limb above knee 15 cm, knee and below knee 5cm for swelling evaluation. Pain scale with Numeric Rating Scale; NRS) before intervention, post-test 1 and post-test 2. Muscle power of knee extensor by the duration with holding knee extension in sitting position before intervention, post-test 1 and post-test 2 Knee range of motion with goniometer in sitting (prone position) The duration of time up and go,6 meter ambulation test with walker usage. ADL evaluation with Barthel Index including transfer score, ambulation score, and up/down stairs score. Paired t-test is applied for statistical significance between these measurements.

      Discussion The investigator expected that post treatment, the patients in the vibration group got increases in knee extensor strength, improvement in calf swelling and functional performance when compared to the control group.

02

Conditions studied

  • Knee Osteoarthritis
  • Arthroplasty Complications
  • Swelling; Leg
03

In context

Osteoarthritis

4,398 studies on the registry are indexed under Osteoarthritis; 582 are open to participants now.

This study's enrollment of 52 is below the median of 70 across 3,440 interventional studies indexed under Osteoarthritis.

Browse Osteoarthritis studies →

Lead sponsor

Kaohsiung Medical University Chung-Ho Memorial Hospital is the lead sponsor of 281 studies on the registry; 57 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • knee osteoarthritis
  • post-operation of total knee arthroplasty
  • single leg knee arthroplasty

Exclusion criteria

Exclusion Criteria:

  • vital signs unstable
  • uncontrolled blood pressure
  • diabetes mellitus
  • neoplasm
  • neurological disorder
  • fibromyalgia
  • cardiac pacemaker
  • musculoskeletal involvement other than TKA
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
52 participants (actual)

Study arms

  • Experimental
    whole body vibration on

    vibration machine on combined with conventional physical therapy

    Device: whole-body vibration

  • Sham comparator
    whole body vibration off

    vibration machine off combined with conventional physical therapy

    Device: whole-body vibration

Interventions

  • Devicewhole-body vibration

    10 minutes WBV exercise in standing position; amplitude 2mm,; frequency 4-10Hz; resting interval: 3 minutes rest.

06

What researchers measure

Primary outcomes

  1. pain scale (Numeric Rating Scale 0-10)

    pain with NRS before and after therapy

    Time frame: 30 seconds

  2. lower leg circumference (cm)

    Above knee 15cm and below knee 5cm circumference before and after therapy

    Time frame: 1 minute

  3. knee range of motion

    knee range of motion in degree with goniometer in supine position

    Time frame: 30 seconds

  4. knee extensor muscle strength

    knee extensor strength with dynamometer in knee flexion 45 degree, in kg in 3 times

    Time frame: 1 minute

Secondary outcomes

  1. Modified five times sit to stand test

    straight back chair with a solid seat 40 cm high. The investigator asked the participants to stand up and sit down as quickly as possible for 5 times, and the time spent were recorded.

    Time frame: 5 minutes

  2. Modified timed up and go (TUG) test

    stand from seat height of 40 cm, walk a distance of 3 meters, turn around, walk back to the chair and sit down

    Time frame: 5 minutes

07

Study locations

1 site
  • Kaohsiung Medical University Hospital
    Kaohsiung, 807, Taiwan
08

References and documents

Publications

  • Park YG, Kwon BS, Park JW, Cha DY, Nam KY, Sim KB, Chang J, Lee HJ. Therapeutic effect of whole body vibration on chronic knee osteoarthritis. Ann Rehabil Med. 2013 Aug;37(4):505-15. doi: 10.5535/arm.2013.37.4.505. Epub 2013 Aug 26. PubMed 24020031 ↗

Study documents

  • Protocol and statistical analysis plan · Jan 14, 2018

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 30, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04107350
Lead sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
Responsible party
Sponsor
First posted
Sep 27, 2019
Start date
Mar 6, 2018
Primary completion
Nov 16, 2018
Completion
Jan 10, 2019
Last update
Sep 30, 2019

Study contacts

Chia-Hsin Chen, PhD
study chair · Kaohsiung Medical University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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