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

NCT ID: NCT04107350

Last Updated: 2019-09-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

52 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-06

Study Completion Date

2019-01-10

Brief Summary

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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.

Detailed Description

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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.

4\. Post-TKA day 3
1. 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.
2. 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.

Conditions

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Knee Osteoarthritis Arthroplasty Complications Swelling; Leg

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

knee osteoarthritis status post total knee arthroplasty receive therapy on post-operation day 2 and post operation day 3 Study group: WBV+conventional physical therapy Control group: convention physical therapy
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
A single-blinded randomized control trial Intervention by the physical therapist Evaluation by the physician

Study Groups

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whole body vibration on

vibration machine on combined with conventional physical therapy

Group Type EXPERIMENTAL

whole-body vibration

Intervention Type DEVICE

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

whole body vibration off

vibration machine off combined with conventional physical therapy

Group Type SHAM_COMPARATOR

whole-body vibration

Intervention Type DEVICE

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

Interventions

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whole-body vibration

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

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* vital signs unstable
* uncontrolled blood pressure
* diabetes mellitus
* neoplasm
* neurological disorder
* fibromyalgia
* cardiac pacemaker
* musculoskeletal involvement other than TKA
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kaohsiung Medical University Chung-Ho Memorial Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chia-Hsin Chen, PhD

Role: STUDY_CHAIR

Kaohsiung Medical University

Locations

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Kaohsiung Medical University Hospital

Kaohsiung City, , Taiwan

Site Status

Countries

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Taiwan

References

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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.

Reference Type BACKGROUND
PMID: 24020031 (View on PubMed)

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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KMUHIRB-F(II)-20170135

Identifier Type: -

Identifier Source: org_study_id