search
Back to results

Combined Effect of Laser Acupuncture and Electroacupuncture in Knee Osteoarthritis Patients

Primary Purpose

Knee Osteoarthritis

Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Laser Acupuncture
Sham Laser Acupuncture
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Electroacupuncture, Laser acupuncture, Low-level laser therapy, Photobiomodulation, Complementary medicine

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • VAS more than 3 point when daily activity
  • Kellgren-Lawrence Grading Scale grade 1 to 3 on knee X-ray
  • Provided informed consent

Exclusion Criteria:

  • History of knee arthroplasty, traumatic injury related joint deformity,
  • Body mass index more than 35
  • pacemaker insertion, photosensitivity
  • who had undergone intra-articular injection or acupuncture in recent one month
  • other factors that may affect the evaluation of the outcome, such as psychiatric disorder or moderate mental retardation etc.

Sites / Locations

  • Chang Gung Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Group A

Group B

Arm Description

True LA with EA

Sham LA with EA

Outcomes

Primary Outcome Measures

Change of Visual Analog Score
Visual Analog Score for pain during activity; change from baseline at 4 weeks; scoring from 0 to 10, and the higher scores indicate the worse condition
Use of analgesics
Frequency of analgesics

Secondary Outcome Measures

Change of the score of Western Ontario and McMaster Universities Arthritis Index
Questionnaires for the function in patients with OA knee; change from baseline at 4 weeks; scoring from 0 to 68, and the higher scores indicate the worse condition
Change of the percentage of Knee Injury and Osteoarthritis Outcome Score
Questionnaires for the function in patients with OA knee; change from baseline at 4 weeks; scoring from 0 to 100 percentage, and the higher percentage indicates the better condition
Change of the muscle stiffness of quadriceps
The value is measured by Myoton Digital Palpation Device; change from baseline at 4 weeks
Change of the angle of knee range of motion
The range between flexion and extension of the knee; change from baseline at 4 weeks
Change of the minutes of standing on one foot test
The patient stands on one foot with hands on hips and eye opening. The time that the patient can stand on one foot was recorded; change from baseline at 4 weeks
Change of the times of 30-second chair stand test
The patient sits on the chair with bilateral feet stepping on the ground and hands cross beyond chest. Then he/she stands up and then sits down. The definition of once is completing one standing up and then sitting down. The number of times that the patient could stand up and then sit down within 30 seconds; change from baseline at 4 weeks.

Full Information

First Posted
December 1, 2019
Last Updated
January 27, 2021
Sponsor
Chang Gung Memorial Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT04188925
Brief Title
Combined Effect of Laser Acupuncture and Electroacupuncture in Knee Osteoarthritis Patients
Official Title
Combined Effect of Laser Acupuncture and Electroacupuncture in Knee Osteoarthritis Patients: a Protocol for a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
December 3, 2019 (Actual)
Primary Completion Date
December 31, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Background: Knee osteoarthritis (KOA) is a common degenerative joint disorder affected 250 million people globally. It can not only result in disability, but also associated with cardiovascular disease and mortality. The most common treatment for KOA is non-steroidal anti-inflammatory drug. However, the effect of analgesic is limited and may complicate with side effect. Hence, many patients search for complementary and alternative medicine. Acupuncture is one of the most popular complementary treatment with good analgesic effect and less side effect. Electroacupuncture (EA) or laser acupuncture (LA) was reported effective in pain control in knee osteoarthritis patients. However, there is no study about combination effect of EA and LA. Methods: This protocol is a randomized controlled trial investigating the combination effect of EA and LA on KOA. Fifty participants diagnosed KOA with aged more than 50 years old and knee pain more than 3 months were recruited and randomly assigned to the experimental group (EA plus LA) or sham group (EA plus LA without laser output) in clinical research center. The subjects will undergo EA plus LA treatment thrice a weeks for 4 weeks. The experimental group will receive acupuncture at GB33, GB34, SP9, SP10, and ST36 with transcutaneous electrical nerve stimulator on the GB34+33 and SP9+10., and the LA deliver 6 Joule of energy at EX-LE5, ST35, and BL40. The subjects in sham group will receive the same way but the LA is without any laser output. Outcome measurement will include visual analogue scale (VAS), Western Ontario McMaster Universities Osteoarthritis Index (WOMAC), Knee injury and osteoarthritis outcome (KOOS), body composition analysis, knee range of motion test, muscle stiffness test, standing on one foot test, and the 30-second chair stand test before intervention and after 4 weeks intervention. The result will be analyze and compared between the experimental group and sham group using the paired t test and one-way analysis of variance. Objectives: The aim of this protocol is to investigate the combination effect of EA and LA in KOA patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Electroacupuncture, Laser acupuncture, Low-level laser therapy, Photobiomodulation, Complementary medicine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Masking Description
Sham LA is using the same appearance of LaserPen without energy output to perform the same acupoint as above description
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Experimental
Arm Description
True LA with EA
Arm Title
Group B
Arm Type
Sham Comparator
Arm Description
Sham LA with EA
Intervention Type
Device
Intervention Name(s)
Laser Acupuncture
Intervention Description
The LA is using a gallium aluminum arsenide LaserPen (maximal power, 150 mW; wavelength, 810nm; area of probe, 0.03cm2; power density, 5W/cm2; pulsed wave; RJ-Laser, Reimers & Janssen GmbH, Waldkirch, Germany). The LA treatment will be applied to EX-LE5, ST35, and BL40 for 80 seconds, under power 150mW, to deliver a total treatment dose of 6 Joule/ cm2. The EA is the combination of acupuncture and transcutaneous electrical nerve stimulator. The transcutaneous electrical nerve stimulator is produced by Ching Ming Medical Device Company. This machine is verified by Department of Health in Taiwan, with the ID number 001147. We perform acupuncture on GB33, GB34, SP9, SP10, and ST36.
Intervention Type
Device
Intervention Name(s)
Sham Laser Acupuncture
Intervention Description
Sham LA is using the same appearance of LaserPen without energy output to perform the same acupoint as above description. Both of the LaserPen in two groups are labeled with A and B, one of them is revised by the company to become the sham LA. The outward of both LaserPen are the same and our physician does not know which one is the real.
Primary Outcome Measure Information:
Title
Change of Visual Analog Score
Description
Visual Analog Score for pain during activity; change from baseline at 4 weeks; scoring from 0 to 10, and the higher scores indicate the worse condition
Time Frame
Through study completion, an average of 4 weeks
Title
Use of analgesics
Description
Frequency of analgesics
Time Frame
Through study completion, an average of 4 weeks
Secondary Outcome Measure Information:
Title
Change of the score of Western Ontario and McMaster Universities Arthritis Index
Description
Questionnaires for the function in patients with OA knee; change from baseline at 4 weeks; scoring from 0 to 68, and the higher scores indicate the worse condition
Time Frame
Through study completion, an average of 4 weeks
Title
Change of the percentage of Knee Injury and Osteoarthritis Outcome Score
Description
Questionnaires for the function in patients with OA knee; change from baseline at 4 weeks; scoring from 0 to 100 percentage, and the higher percentage indicates the better condition
Time Frame
Through study completion, an average of 4 weeks
Title
Change of the muscle stiffness of quadriceps
Description
The value is measured by Myoton Digital Palpation Device; change from baseline at 4 weeks
Time Frame
Through study completion, an average of 4 weeks
Title
Change of the angle of knee range of motion
Description
The range between flexion and extension of the knee; change from baseline at 4 weeks
Time Frame
Through study completion, an average of 4 weeks
Title
Change of the minutes of standing on one foot test
Description
The patient stands on one foot with hands on hips and eye opening. The time that the patient can stand on one foot was recorded; change from baseline at 4 weeks
Time Frame
Through study completion, an average of 4 weeks
Title
Change of the times of 30-second chair stand test
Description
The patient sits on the chair with bilateral feet stepping on the ground and hands cross beyond chest. Then he/she stands up and then sits down. The definition of once is completing one standing up and then sitting down. The number of times that the patient could stand up and then sit down within 30 seconds; change from baseline at 4 weeks.
Time Frame
Through study completion, an average of 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: VAS more than 3 point when daily activity Kellgren-Lawrence Grading Scale grade 1 to 3 on knee X-ray Provided informed consent Exclusion Criteria: History of knee arthroplasty, traumatic injury related joint deformity, Body mass index more than 35 pacemaker insertion, photosensitivity who had undergone intra-articular injection or acupuncture in recent one month other factors that may affect the evaluation of the outcome, such as psychiatric disorder or moderate mental retardation etc.
Facility Information:
Facility Name
Chang Gung Memorial Hospital
City
Kaohsiung
ZIP/Postal Code
833
Country
Taiwan

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Combined Effect of Laser Acupuncture and Electroacupuncture in Knee Osteoarthritis Patients

We'll reach out to this number within 24 hrs