Pregnancy-Related Low Back Pain and Complementary and Alternative Medicine (CAM) Treatment

Sponsor
Oregon Health and Science University (Other)
Overall Status
Completed
CT.gov ID
NCT00937365
Collaborator
The ONE Foundation (Other)
64
1
3
33
1.9

Study Details

Study Description

Brief Summary

This study compares three treatments for low back pain that started during pregnancy. The study hypothesizes that exercise, spinal manipulation, and a mind-body technique called neuroemotional technique (NET) equally affect pain intensity and disability associated with pregnancy-related low back pain. The study also hypothesizes that pain intensity and disability levels do not influence maternal heart rate variability (a measure of stress) and intrauterine attachment (a measure of relationship quality). Ten women will additionally provide blood and salivary oxytocin samples during pregnancy and periodically for three months after birth. These women and their babies will also be videotaped playing for 5 minutes at 2 weeks, 6 weeks, and 3 months postpartum.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise
  • Procedure: Spinal Manipulation
  • Procedure: Neuroemotional Technique (NET)
Phase 2

Detailed Description

Pregnancy-related low back pain is experienced by over half of all pregnant women. In the United States it is thought of as a normal constituent of pregnancy. However, in Europe low back pain associated with pregnancy is treated. In the United States pregnancy-related low back pain is thought to resolve with birth. However about 1/3 of women who experience pregnancy-related low back pain continue to experience back pain for one year postpartum. Those women whose low back pain persists into the postpartum period are more at risk of experiencing comorbidities such as postpartum depression.

In the extrauterine life maternal pain limits a mother's ability to securely attach with her child. Furthermore, interpretation of pain intensity is influenced by the type of attachment the individual has with her parents. Little is known how maternal pain may influence intrauterine attachment. Similarly, heart rate variability is influenced by pain and by spinal manipulation in non-pregnant populations. However, normal non-pregnant patterns of heart rate variability are altered during the second and third trimesters of pregnancy, and little is known about why this happens or what this means.

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Pilot Randomized Controlled Trial for Complementary and Alternative Medicine Treatment of Pregnancy-Related Low Back Pain.
Study Start Date :
Jul 1, 2009
Actual Primary Completion Date :
Apr 1, 2012
Actual Study Completion Date :
Apr 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Exercise

Specific strengthening exercises demonstrated to improve pregnancy-related low back pain are taught to participants of this arm. Additionally, each participant will be evaluated and additional exercises will be prescribed relevant to her particular needs. Study participants of this arm are asked to perform the exercises at home at least once a day. Exercise is recorded in a diary. Participants follow the same study visit schedule as the two other arms.

Behavioral: Exercise
Study visits follow the normal prenatal care schedule (once monthly until 28 weeks, twice monthly until 36 weeks, weekly thereafter). Additional study visits may be necessary if the pain is too intense and requires additional visits.
Other Names:
  • pelvic tilts
  • stretch
  • strengthen
  • glut squeeze
  • Experimental: Spinal Manipulation

    Women randomized to this arm will be evaluated for spinal subluxations and, if appropriate, treated with chiropractic manipulation. Type of manipulation is determined by presentation. Woman may be manipulated with high velocity low amplitude thrust, blocking, activator, or other appropriate means of manipulating.

    Procedure: Spinal Manipulation
    Study visits follow the normal prenatal care schedule (once monthly until 28 weeks, twice monthly until 36 weeks, weekly thereafter). Additional study visits may be necessary if the pain is too intense and requires additional visits.
    Other Names:
  • SMT
  • CMT
  • chiropractic manipulative therapy
  • OMT
  • osteopathic manipulative therapy
  • adjustment
  • Experimental: Neuroemotional technique (NET)

    Neuroemotional technique (NET) is a mind-body technique which combines elements of chiropractic medicine, Chinese medicine, and behavioral psychology. Muscle response testing, a form of functional neurology, and visceral somatic reflexes are used to ascertain whether the pain or dysfunction experienced by the participant has an emotional component. If an emotional component is present, it is identified and the original "triggering" occurrence is identified. The participant creates a snapshot of that original occurrence and while she holds that image in her mind spinal levels which innervate the associated organ are adjusted.

    Procedure: Neuroemotional Technique (NET)
    Study visits follow the normal prenatal care schedule (once monthly until 28 weeks, twice monthly until 36 weeks, weekly thereafter). Additional study visits may be necessary if the pain is too intense and requires additional visits.
    Other Names:
  • NET
  • Mind-body therapy
  • Outcome Measures

    Primary Outcome Measures

    1. Roland Morris Disability Index [Last study visit prior to birth]

    Secondary Outcome Measures

    1. Pain Visual Analog Scale [Last Study Visit Before Birth]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 49 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Healthy

    • 20-49 years old

    • Pregnant with a singleton

    • Low back pain began during pregnancy and has lasted more than one week

    • Low back pain is reproducible with palpation

    Exclusion Criteria:
    • Health conditions such as hypertension, diabetes, cancer, thyroid condition etc.

    • Pain radiates below knee

    • Cannot read English

    • Plans to move away from Portland area during pregnancy

    • Not willing to be randomized to one of the three arms of the study

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Oregon Health & Science University Portland Oregon United States 97239

    Sponsors and Collaborators

    • Oregon Health and Science University
    • The ONE Foundation

    Investigators

    • Principal Investigator: Thomas Gregory, MD, Oregon Health and Science University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Oregon Health and Science University
    ClinicalTrials.gov Identifier:
    NCT00937365
    Other Study ID Numbers:
    • 5033
    First Posted:
    Jul 13, 2009
    Last Update Posted:
    Dec 18, 2019
    Last Verified:
    Dec 1, 2019

    Study Results

    No Results Posted as of Dec 18, 2019