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Electro-acupuncture (EA) and Chronic Pelvic Pain (CPP) (BMEA)

Primary Purpose

Chronic Pain

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
EA treatment
TCM health consult
Usual Care
Sponsored by
University of Edinburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pain focused on measuring electro-acupuncture, chronic pelvic pain, patient practitioner interactions, TCM health consultation, meridian balanced method acupuncture

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Chronic pelvic pain longer than 6 months duration
  • Average numerical pain score of at least 4 out of 10 in the previous week
  • Able and willing to comply with intervention
  • Women aged 18 and above

Exclusion Criteria:

  • Pregnancy
  • Malignancy
  • Severe bleeding disorders (e.g. Type 2, 3 Von Willebrand disease)
  • Severe needle phobia
  • Taking anti-coagulants
  • A history of seizure
  • A pace-maker in situ
  • Moderate to severe psychiatric illness (currently under the care of a psychiatrist)
  • Had received electro-acupuncture and meridian balanced method within the last 6 months

Sites / Locations

  • Ooi Thye Chong

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Active Comparator

Arm Label

EA treatment and TCM health consult

TCM health consult

Usual care

Arm Description

Participants randomized to the EA treatment will receive 2 EA +TCM health consult once a week x 4 weeks (8 total)

Participants randomized to TCM health consult will receive 2 TCM health consult once a week x 4 weeks ( 8 total)

Participants randomized to usual care will continue with their usual care

Outcomes

Primary Outcome Measures

The primary objective is to determine whether it is possible to achieve acceptable recruitment and retention rates within defined inclusion/exclusion criteria.
We aim to recruit 30 women with CPP in NHS Lothian over a 12-month period and randomise them to BMEA treatment, TCM HC or standard care (SC). Response to the intervention will be monitored by validated pain, physical and emotional functioning questionnaires at weeks 0 (baseline), 4 (end of study) 8 and 12. Focus group discussion to gain feedback on study experience will be conducted at the completion of the study.

Secondary Outcome Measures

The secondary objectives are to determine the effectiveness and acceptability to patients of the proposed methods of recruitment, randomisation, interventions and assessment tools.
We aim to recruit 30 women with CPP in NHS Lothian over a 12-month period and randomise them to BMEA treatment, TCM HC or standard care (SC). Response to the intervention will be monitored by validated pain, physical and emotional functioning questionnaires at weeks 0 (baseline), 4 (end of study) 8 and 12. Focus group discussion to gain feedback on study experience will be conducted at the completion of the study.
VAS Scale
Questionnaire
Brief Pain Inventory
Questionnaire
Hospital Anxiety and Depression Scale
Questionnaire
SF 12
Questionnaire
Work Productivity & Activity Impairment Questionnaire
Questionnaire
Sexual Activity Questionnaire
Questionnaire
Pain Catastrophising Questionnaire
Questionnaire
Focus Group Discussions
Qualitative Method

Full Information

First Posted
September 23, 2014
Last Updated
November 10, 2015
Sponsor
University of Edinburgh
Collaborators
NHS Lothian
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1. Study Identification

Unique Protocol Identification Number
NCT02295111
Brief Title
Electro-acupuncture (EA) and Chronic Pelvic Pain (CPP)
Acronym
BMEA
Official Title
The BMEA Study: The Impact of Meridian Balanced Method (BM) Electro-acupuncture (EA) Treatment on Women With Chronic Pelvic Pain (CPP): A Three-arm Randomized Controlled Pilot Study.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Edinburgh
Collaborators
NHS Lothian

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic pelvic pain (CPP) is a debilitating condition that affects over 1 million women in the United Kingdom. The annual healthcare costs are estimated at over £150 million. Proven interventions which include the use of analgesics or hormonal treatments are unsatisfactory in many cases. The investigators believe that the meridian balance method (BM) electro-acupuncture (EA) treatment (which includes a Traditional Chinese Medicine Health Consultation [TCM HC]) may be helpful in the management of CPP. Studies on the mechanisms of EA have demonstrated an analgesic effect. A recent individual patient data meta-analysis on the use of acupuncture for four chronic pain conditions found a small statistically significant effect size when compared to sham acupuncture. The effect size was larger and statistically significant when compared to usual care controls. This meta-analysis, and other large studies, suggests that, in addition to this analgesic effect, the interaction between the patient and the healthcare provider also plays a role in its effect on painful symptoms. Our hypothesis is that the meridian BMEA treatment alleviates pain, and improves physical and emotional functioning, in women with CPP. The investigators plan to undertake a single centre pilot study to assess the feasibility of performing a future three-armed randomised controlled, parallel group design trial to determine the efficacy of the meridian balance method electro-acupuncture (BMEA) treatment in the management of women with CPP. The primary objective is to determine whether it is possible to achieve acceptable recruitment and retention rates within defined inclusion/exclusion criteria. The secondary objectives are to determine the effectiveness and acceptability to patients of the proposed methods of recruitment, randomisation, interventions and assessment tools. The investigators aim to recruit 30 women with CPP in NHS Lothian over a 12-month period and randomise them to BMEA treatment, TCM HC or standard care (SC). Response to the intervention will be monitored by validated pain, physical and emotional functioning questionnaires at weeks 0 (baseline), 4 (end of study) 8 and 12. Focus group discussion to gain feedback on study experience will be conducted at the completion of the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain
Keywords
electro-acupuncture, chronic pelvic pain, patient practitioner interactions, TCM health consultation, meridian balanced method acupuncture

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
EA treatment and TCM health consult
Arm Type
Active Comparator
Arm Description
Participants randomized to the EA treatment will receive 2 EA +TCM health consult once a week x 4 weeks (8 total)
Arm Title
TCM health consult
Arm Type
Experimental
Arm Description
Participants randomized to TCM health consult will receive 2 TCM health consult once a week x 4 weeks ( 8 total)
Arm Title
Usual care
Arm Type
Active Comparator
Arm Description
Participants randomized to usual care will continue with their usual care
Intervention Type
Device
Intervention Name(s)
EA treatment
Intervention Description
Electro acupuncture and traditional Chinese Medicine Health consult
Intervention Type
Behavioral
Intervention Name(s)
TCM health consult
Intervention Description
Traditional Chinese Medicine Health Consult without needling
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Standard NHS care
Primary Outcome Measure Information:
Title
The primary objective is to determine whether it is possible to achieve acceptable recruitment and retention rates within defined inclusion/exclusion criteria.
Description
We aim to recruit 30 women with CPP in NHS Lothian over a 12-month period and randomise them to BMEA treatment, TCM HC or standard care (SC). Response to the intervention will be monitored by validated pain, physical and emotional functioning questionnaires at weeks 0 (baseline), 4 (end of study) 8 and 12. Focus group discussion to gain feedback on study experience will be conducted at the completion of the study.
Time Frame
At the end of study: 12 months from start of study
Secondary Outcome Measure Information:
Title
The secondary objectives are to determine the effectiveness and acceptability to patients of the proposed methods of recruitment, randomisation, interventions and assessment tools.
Description
We aim to recruit 30 women with CPP in NHS Lothian over a 12-month period and randomise them to BMEA treatment, TCM HC or standard care (SC). Response to the intervention will be monitored by validated pain, physical and emotional functioning questionnaires at weeks 0 (baseline), 4 (end of study) 8 and 12. Focus group discussion to gain feedback on study experience will be conducted at the completion of the study.
Time Frame
12 months from date of recruitment
Title
VAS Scale
Description
Questionnaire
Time Frame
At 0, 4, 8, 12 weeks
Title
Brief Pain Inventory
Description
Questionnaire
Time Frame
At 0, 4, 8, 12 weeks
Title
Hospital Anxiety and Depression Scale
Description
Questionnaire
Time Frame
at 0, 4, 8, 12 weeks
Title
SF 12
Description
Questionnaire
Time Frame
at 0, 4, 8, 12 weeks
Title
Work Productivity & Activity Impairment Questionnaire
Description
Questionnaire
Time Frame
at 0, 4, 8, 12 weeks
Title
Sexual Activity Questionnaire
Description
Questionnaire
Time Frame
at 0, 4, 8, 12 weeks
Title
Pain Catastrophising Questionnaire
Description
Questionnaire
Time Frame
at 0, 4, 8, 12 weeks
Title
Focus Group Discussions
Description
Qualitative Method
Time Frame
At the end of study

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic pelvic pain longer than 6 months duration Average numerical pain score of at least 4 out of 10 in the previous week Able and willing to comply with intervention Women aged 18 and above Exclusion Criteria: Pregnancy Malignancy Severe bleeding disorders (e.g. Type 2, 3 Von Willebrand disease) Severe needle phobia Taking anti-coagulants A history of seizure A pace-maker in situ Moderate to severe psychiatric illness (currently under the care of a psychiatrist) Had received electro-acupuncture and meridian balanced method within the last 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie Fallon, MD PhD
Organizational Affiliation
University of University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ooi Thye Chong
City
Edinburgh
State/Province
City of Edinburgh
ZIP/Postal Code
EH16 4SA
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
26576808
Citation
Chong OT, Critchley HO, Horne AW, Elton R, Haraldsdottir E, Fallon M. The BMEA study: the impact of meridian balanced method electroacupuncture on women with chronic pelvic pain-a three-arm randomised controlled pilot study using a mixed-methods approach. BMJ Open. 2015 Nov 17;5(11):e008621. doi: 10.1136/bmjopen-2015-008621.
Results Reference
derived

Learn more about this trial

Electro-acupuncture (EA) and Chronic Pelvic Pain (CPP)

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