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Trial of Acupuncture Pelvic and Low Back Pain in Pregnancy (Medical and Economical Assessment) (GAME)

Primary Purpose

Disorder of Pregnancy

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
acupuncture
usual care
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Disorder of Pregnancy focused on measuring Pregnancy, Acupuncture, Pelvic and low back pain, Impairment, Economic evaluation

Eligibility Criteria

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

Inclusion Criteria:

  • singleton uncomplicated 16-34 weeks pregnancy, with PLBP > 4/10

Exclusion Criteria:

  • Obstetrical complication other than PLBP,
  • contra indication to acupuncture,
  • sciatica
  • maternal age < 18
  • no health insurance.

Sites / Locations

  • Centre d'Investigation Clinique Paris Est - Hôpital Pitié Salpêtrière

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

acupuncture

usual care

Arm Description

5 acupuncture sessions over a 4 week period plus standard treatment

standard treatment (pregnancy belt, behavioral recommendations, exercises, pain killers as prescribed by usual health care professional)

Outcomes

Primary Outcome Measures

Number and % of days during pregnancy with maximum pain ≤ 4/10.
daily recording on logbook (self assessment)

Secondary Outcome Measures

Mean Oswestry disability score
Number and % of days with maximum pain ≤ 4/10.
direct and indirect costs
direct costs related to pregnancy care and pain management, indirect costs related to impairment throughout pregnancy and the immediate postpartum.

Full Information

First Posted
March 6, 2013
Last Updated
May 24, 2019
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT01848587
Brief Title
Trial of Acupuncture Pelvic and Low Back Pain in Pregnancy (Medical and Economical Assessment)
Acronym
GAME
Official Title
Trial of Acupuncture Pelvic and Low Back Pain in Pregnancy (TAPPP)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2014
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Pelvic girdle and low back pain are common in pregnancy, and cause severe impairment in 10% of women. Our hypothesis is that offering acupuncture in addition to standard care would reduce pain and impairment throughout pregnancy. 300 pregnant women from 5 maternity units will be randomized over a 3 year period to receive standard care or standard care plus acupuncture. Main outcome will be the number of days during pregnancy with maximum pain ≤ 4/10. Secondary outcomes will compare groups for an impairment score and for direct and indirect costs.
Detailed Description
Background. Pelvic and low back pain (PLBP) affects 30% of pregnant women for weeks or months, causing severe impairment in 10% of women. Standard treatment, based on pain killers, postural recommendations, exercises, is of limited value. Previous trials showed that adding acupuncture to standard treatment reduces pain and impairment in the short run. Hypothesis Providing acupuncture to pregnant women with PLBP could reduce pain and impairment throughout pregnancy, thus reducing other direct and indirect cots related to PLBP. Primary Outcome. Number and % of days during pregnancy with maximum pain ≤ 4/10. Secondary Outcomes. Pain scale 4 weeks after inclusion, mean Oswestry disability score between inclusion and delivery, direct costs related to pregnancy care and pain management, indirect costs related to impairment throughout pregnancy and the immediate postpartum. Method. Multicenter randomized trial with parallel groups. Intervention: 5 acupuncture sessions over 4 weeks, plus standard treatment. Controls: standard treatment. Analysis per pregnancy Follow up: logbook kept by he patient plus analysis of obstetrical records. Number of patients: 300 Inclusion criteria: singleton uncomplicated 16-34 weeks pregnancy, with PLBP > 4/10 Exclusion criteria Obstetrical complication other than PLBP, contra indication to acupuncture, sciatica, maternal age < 18, no health insurance. Duration. Overall duration: 3 years and 6 months, inclusions over 3 years. Duration of inclusion per patient: 2-26 weeks Number of participating centers 5

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Disorder of Pregnancy
Keywords
Pregnancy, Acupuncture, Pelvic and low back pain, Impairment, Economic evaluation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
acupuncture
Arm Type
Experimental
Arm Description
5 acupuncture sessions over a 4 week period plus standard treatment
Arm Title
usual care
Arm Type
Active Comparator
Arm Description
standard treatment (pregnancy belt, behavioral recommendations, exercises, pain killers as prescribed by usual health care professional)
Intervention Type
Other
Intervention Name(s)
acupuncture
Intervention Type
Other
Intervention Name(s)
usual care
Primary Outcome Measure Information:
Title
Number and % of days during pregnancy with maximum pain ≤ 4/10.
Description
daily recording on logbook (self assessment)
Time Frame
at 4 weeks
Secondary Outcome Measure Information:
Title
Mean Oswestry disability score
Time Frame
during pregnancy
Title
Number and % of days with maximum pain ≤ 4/10.
Time Frame
during pregnancy
Title
direct and indirect costs
Description
direct costs related to pregnancy care and pain management, indirect costs related to impairment throughout pregnancy and the immediate postpartum.
Time Frame
during pregnancy

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: singleton uncomplicated 16-34 weeks pregnancy, with PLBP > 4/10 Exclusion Criteria: Obstetrical complication other than PLBP, contra indication to acupuncture, sciatica maternal age < 18 no health insurance.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Dommergues, Md, PhD
Organizational Affiliation
APHP
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre d'Investigation Clinique Paris Est - Hôpital Pitié Salpêtrière
City
Paris
ZIP/Postal Code
75013
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
31009470
Citation
Nicolian S, Butel T, Gambotti L, Durand M, Filipovic-Pierucci A, Mallet A, Kone M, Durand-Zaleski I, Dommergues M. Cost-effectiveness of acupuncture versus standard care for pelvic and low back pain in pregnancy: A randomized controlled trial. PLoS One. 2019 Apr 22;14(4):e0214195. doi: 10.1371/journal.pone.0214195. eCollection 2019.
Results Reference
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Trial of Acupuncture Pelvic and Low Back Pain in Pregnancy (Medical and Economical Assessment)

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