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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01595451
Other study ID # 2011P000757
Secondary ID
Status Completed
Phase N/A
First received May 8, 2012
Last updated November 27, 2017
Start date January 2012
Est. completion date October 2017

Study information

Verified date November 2017
Source Brigham and Women's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

We are doing this study to investigate the effects of acupuncture on chronic low back pain. We are interested in learning about brain activity during pain. We plan to look at brain activity at the beginning and the end of the study, after 6 sessions of acupuncture treatment. You will be randomly assigned to one of two groups to receive either real or placebo acupuncture.

Acupuncture has been used for many years to help relieve pain. However, it is not clear how acupuncture works. Acupuncture may relieve pain by changing activity in the nervous system. Some studies indicate that acupuncture may relieve the low back pain. However, we need more research to see how well acupuncture works to relieve pain for people with this condition.

In this study, we will measure your brain activity before and after you do exercises to make your back pain worse. We will also measure your brain activity while inflating a pressure cuff device on your lower leg. We will measure this brain activity using a research tool called functional MRI (fMRI). Functional MRI is a very fast MRI that uses radio waves and a magnet, and allows the study investigators to look at changes in blood flow to different parts of the brain when there are changes in brain activity.


Recruitment information / eligibility

Status Completed
Enrollment 79
Est. completion date October 2017
Est. primary completion date May 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Meet the Classification Criteria of the chronic LBP (having low back pain for more than 6 months), as determined by the referring physician.

- Subjects must be able to provoke or exacerbate their cLBP using our calibrated exercise-like maneuver.

- At least 4/10 clinical pain on the 11-point LBP severity scale on average during the past two weeks prior to enrollment.

- At least a 10th grade English-reading level; English can be a second language provided that the patients feel they understand all the questions used in the assessment measures.

- Right handed individuals

- Must have had a prior evaluation of their low back pain by a health care provider, which may include radiographic studies. Documentation of this evaluation will be obtained from subject's medical record.

Exclusion Criteria:

- Specific causes of back pain (e.g., cancer, fractures, spinal stenosis, infections)

- Complicated back problems (e.g., prior back surgery, medico-legal issues)

- Possible contraindications for acupuncture (e.g., coagulation disorders, cardiac pacemakers, pregnancy, seizure disorder), and conditions that might confound treatment effects or interpretation of results (e.g., severe fibromyalgia, rheumatoid arthritis)

- Conditions making treatment difficult (e.g., paralysis, psychoses, or other severe psychiatric problems based on the judgment of a physician investigator and/or a T score >60 on the psychological assessments performed during Session 1)

- Prior acupuncture treatment for back pain; 1 year minimum for any other condition.

- The intent to undergo surgery during the time of involvement in the study.

- History of cardiac, respiratory, or nervous system disease that, in the judgment of a physician investigator, precludes participation in the study because of a heightened potential for adverse outcome (e.g., asthma, claustrophobia)

- Presence of any contraindications to MRI scanning (e.g., cardiac pacemaker, metal implants, fear of closed spaces, pregnancy)

- Active substance abuse disorders within the last 24 months, based on subject self-report

- Unresolved medical legal/disability/workers compensation claims

- Radicular knee pain extending below the knee

- Use of more than 60 mg morphine equivalent prescription opioids or steroids for pain.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Acupuncture
A licensed acupuncturist will perform acupuncture for six, 30 minute treatment sessions.

Locations

Country Name City State
United States MGH - Martinos Center Charlestown Massachusetts

Sponsors (3)

Lead Sponsor Collaborator
Brigham and Women's Hospital Massachusetts General Hospital, National Center for Complementary and Integrative Health (NCCIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain improvement in patients with lower back pain Acupuncture in patients with lower back pain 6 week study
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