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Warm Needle Acupuncture vs Needle Acupuncture

Primary Purpose

Osteoarthritis, Knee

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Warm needle acupuncture
Needle acupuncture
Sponsored by
London South Bank University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Bi syndrome

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Chronic pain in at least one knee joint during the last six months.
  • At baseline the WOMAC pain score must be ≥ 3 points (on a scale of 0-10)

In addition to the knee pain at least 3 of the following 6 must be present:

  • Age > 50 years
  • Stiffness < 30 minutes
  • Crepitus
  • Bony Tenderness
  • Bony enlargement
  • No palpable warmth

(ACR 2013)

Plus

  • Ability to speak English
  • Signed consent form

Exclusion Criteria:

  • A systemic disease of the musculoskeletal system.
  • Bone tumour, bone tumour like lesions or metastasis.
  • Bone fracture in the lower extremities during the last three months.
  • Acute infection or osteonecrosis in the knee joint.
  • Recent sprain injury to the knee joint.
  • Surgery of the afflicted extremity during the last six months or planned surgery.
  • Ongoing cortico-steroid therapy or cortisone injections in the past six weeks.
  • Taking anti-coagulant medication.
  • Coagulopathy.
  • Other pain condition that compels the patient to take analgesics for more than three days during the last four weeks.
  • Addiction to analgesics, opiate or other drugs.
  • Acupuncture treatment in the past 3 months.
  • Dermatological disease within the acupuncture area impairing acupuncture treatment.
  • Pregnant or breast-feeding patients.
  • Inability to follow instructions or understand the consent form (insufficient command of language, dementia).
  • Participation in another clinical study.
  • Ongoing legal proceedings concerning degree of disability.

Sites / Locations

  • Confucius Institute for TCM LSBU

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Warm needle acupuncture

Basic needle acupuncture

Arm Description

Warm needle acupuncture (wenzhen; 温针) is where moxa cones are placed on the handle of the needle, after the needle has been inserted. Once lit, heat transmits along the shaft of the needle to the acupuncture point. Moxa refers to the herb mugwort (Artemisia vulgaris) that is burnt to warm specific parts of the body, including acupuncture points.

Basic needle acupuncture is the use of acupuncture needles alone, without other methods of stimulation.

Outcomes

Primary Outcome Measures

Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

Secondary Outcome Measures

SF36 (Rand)
Health Related Quality of Life (HRQL)

Full Information

First Posted
February 4, 2016
Last Updated
April 20, 2017
Sponsor
London South Bank University
Collaborators
British Acupuncture Council, Confucius Institute for Traditional Chinese Medicine, London South Bank University
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1. Study Identification

Unique Protocol Identification Number
NCT02680912
Brief Title
Warm Needle Acupuncture vs Needle Acupuncture
Official Title
Warm Needle Acupuncture vs. Needle Acupuncture for Osteoarthritis of the Knee: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
May 16, 2017 (Anticipated)
Study Completion Date
July 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
London South Bank University
Collaborators
British Acupuncture Council, Confucius Institute for Traditional Chinese Medicine, London South Bank University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a two-armed randomised controlled pilot study that investigates the component efficacy of moxibustion for osteoarthritis of the knee. Participants will be randomised to receive either warm needle acupuncture or needle acupuncture. Participants and acupuncturists will be blinded to group allocation. The primary and secondary outcome measures are WOMAC and SF36 respectively. Qualitative interviews will be used to gather information on the patients' experiences and perceptions of the trial and the treatment provided. It is hypothesised that warm needle acupuncture will lead to a greater reduction in clinical signs and symptoms than needle acupuncture.
Detailed Description
Acupuncture Treatment All participants will receive acupuncture. Only points local to the knee will be used. There will be 4-6 points used per knee, therefore 8 -12 needles per treatment. A record will be kept of the points used at each treatment. Both knees will be treated even if only one knee is painful. This will ensure that participants receive similar treatments. Patients will be treated seated, as this allows better access to the relevant acupuncture points. It also helps ensure the moxibustion is carried out safely. Participants will receive 8 treatments in the first 4 weeks (twice a week), then 4 treatments in 4 weeks (once a week). Blinding procedures The only difference in the procedures will be that lit cones are placed on the needles of the treatment group whilst unlit moxa cones will be placed on the needles of the control group. Smokeless moxa will be used. All patients will see the needles being inserted and the moxa cones placed on the needles by the acupuncturist. Skin guards will be placed at the base of the needle to reduce the immediate sense of heat on the surface of the skin. Similar skin guards are routinely used in acupuncture treatment to prevent any discomfort. The acupuncturist will carry out a consultation at each session as per normal practice. After the needles have been inserted and the moxa cones have been placed on needles the acupuncturist leaves and an assistant acupuncturist enters the room. The assistant acupuncturist will place a screen in front of the patient to prevent them from seeing their knees. The assistant acupuncturist will then remove one cone at a time and light it. In the treatment group the lit cone is placed on the needle. In the control group the lit cone is place in a small dish close to the knee, a replacement unlit cone is placed on the needle. This process is repeated until all the cones are lit. The unlit cone is replaced on the needle of the control group to try and ensure they experience the same sensations as the treatment group. The use of a second acupuncturist to light the moxa ensures that the acupuncturist who carries out the consultation and inserts the needles is blinded to group allocation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
Bi syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Warm needle acupuncture
Arm Type
Experimental
Arm Description
Warm needle acupuncture (wenzhen; 温针) is where moxa cones are placed on the handle of the needle, after the needle has been inserted. Once lit, heat transmits along the shaft of the needle to the acupuncture point. Moxa refers to the herb mugwort (Artemisia vulgaris) that is burnt to warm specific parts of the body, including acupuncture points.
Arm Title
Basic needle acupuncture
Arm Type
Active Comparator
Arm Description
Basic needle acupuncture is the use of acupuncture needles alone, without other methods of stimulation.
Intervention Type
Device
Intervention Name(s)
Warm needle acupuncture
Intervention Description
There will be 4-6 points used per knee, therefore 8-12 needles per treatment. Two points will be used as the core treatment ST 35 dubi, Ex-LE 5 xiyan. Four other acu-points can also be used from the following: Ahshi painful points local to the knee (locus dolendi), ST 36 zusanli, GB 34 yanglingquan, Sp 9 yinlingquan, ST34 liangqiu, Sp 10 xuehai, GB 33 yangxiguan, LR 7 xiguan, LR 8 ququan, heding Ex-LE 2 In addition to the acupuncture needles the warm needle acupuncture group will receive moxibustion on up to 4 points. Smokeless moxa will be used.
Intervention Type
Device
Intervention Name(s)
Needle acupuncture
Intervention Description
The point selection protocol will be exactly the same as the experimental group
Primary Outcome Measure Information:
Title
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Time Frame
Change from Baseline to follow up at 16 weeks
Secondary Outcome Measure Information:
Title
SF36 (Rand)
Description
Health Related Quality of Life (HRQL)
Time Frame
Change from Baseline to follow up at 16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic pain in at least one knee joint during the last six months. At baseline the WOMAC pain score must be ≥ 3 points (on a scale of 0-10) In addition to the knee pain at least 3 of the following 6 must be present: Age > 50 years Stiffness < 30 minutes Crepitus Bony Tenderness Bony enlargement No palpable warmth (ACR 2013) Plus Ability to speak English Signed consent form Exclusion Criteria: A systemic disease of the musculoskeletal system. Bone tumour, bone tumour like lesions or metastasis. Bone fracture in the lower extremities during the last three months. Acute infection or osteonecrosis in the knee joint. Recent sprain injury to the knee joint. Surgery of the afflicted extremity during the last six months or planned surgery. Ongoing cortico-steroid therapy or cortisone injections in the past six weeks. Taking anti-coagulant medication. Coagulopathy. Other pain condition that compels the patient to take analgesics for more than three days during the last four weeks. Addiction to analgesics, opiate or other drugs. Acupuncture treatment in the past 3 months. Dermatological disease within the acupuncture area impairing acupuncture treatment. Pregnant or breast-feeding patients. Inability to follow instructions or understand the consent form (insufficient command of language, dementia). Participation in another clinical study. Ongoing legal proceedings concerning degree of disability.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ian K Appleyard
Organizational Affiliation
London South Bank University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Confucius Institute for TCM LSBU
City
London
ZIP/Postal Code
SE1 0AA
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.womac.org/
Description
WOMAC Osteoarthritis Index
URL
http://www.rheumatology.org/practice/clinical/classification/oaknee.asp
Description
ACR 2013, "Classification Criteria for Rheumatic Diseases: Idiopathic OA of the knee", American College of Rheumatology, [Online], , pp. 5 January 2014.

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Warm Needle Acupuncture vs Needle Acupuncture

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