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Clinical Trials/NCT00545623
NCT00545623CompletedPhase 2

Acupuncture and Relaxation Response for GI Symptoms and HIV Medication Adherence

Boston University1 site in 1 country130 target enrollmentStarted: April 1, 2007Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
130
Locations
1
Primary Endpoint
Changes in GI Symptom Per Intervention Session

Study Overview

Brief Summary

The aims of the study are to investigate individual, combined and added effects of acupuncture and the relaxation response in reducing gastrointestinal symptoms, improving medication adherence and quality of life among people living with HIV/AIDS. The study will also explore the mechanism of these therapeutic effects of acupuncture and the relaxation response.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Confirmed HIV-positive status or AIDS diagnosis
  • •Self report of having at least one of the 6 GI symptoms: diarrhea, loose stools, gas/flatulence or bloating, abdominal pain, nausea, or vomiting that have persisted for at least 8 weeks.
  • •Being on a stable antiretroviral regimen containing Nucleoside/nucleotide reverse transcriptase inhibitors and/or protease inhibitors- for at least 8 weeks.

Exclusion Criteria

  • •Incident diagnosis of any of the following conditions within the past month or during study period: Pneumocystis carinii pneumonia, Kaposi's sarcoma, Mycobacterium avian complex, Cytomegalovirus, Non-Hodgkins lymphoma, Lymphoma or other cancer, Pelvic inflammatory disease, AIDS-related dementia, Bacterial or other infection, Diabetes, Acute moderate or severe neutropenia, Cryptococcus, Progressive multifocal leukoencephalopathy, Idiopathic thrombocytopenic purpura. All of these conditions are major opportunistic infections or medical complications that may require hospitalization and additional pharmaceutical intervention.
  • •GI diagnoses of irritable bowel syndrome, Crohn's Disease, parasites, any type of gastric ulcer or ulcerative colitis or cancer in any part of the gastrointestinal system. These are conditions not related to HIV diagnosis and could result in digestive problems similar to those we are investigating.
  • •Onset of acute opportunistic infection.
  • •Hemophilia or other bleeding disorder since that will make acupuncture treatment unsafe.
  • •Pregnant women will be excluded since, although none of the acupuncture points or combinations are contraindicated in pregnancy, the presence of morning sickness could serve as a potential confounding factor.
  • •Current users of acupuncture for treating GI symptoms.
  • •Current practice of relaxation response.
  • •Current enrollment in another clinical intervention study.
  • •Cognitive impairment as measured by Mini Mental Status Examination (MMSE), a reliable and valid screening instrument for the detection of cognitive impairment, using a commonly used cut-off point of
  • •If use of Chinese herbs has been recently discontinued, a potential participant must have at least 2 weeks without herb use to be eligible for the study. Because use of herbs is occasionally accompanied by digestive disorders,a period of stabilizing is required before acupuncture treatment can be initiated. This washout period has been conservatively estimated by ACP staff herbalists to constitute a sufficient time for effects of herbs to cease.

Arms & Interventions

ACU+RR

Active Comparator

acupuncture + relaxation response CD

Intervention: Acupuncture (Procedure)

ACU+RR

Active Comparator

acupuncture + relaxation response CD

Intervention: Relaxation Response (Behavioral)

SHAM+RR

Active Comparator

sham acupuncture + relaxation response CD

Intervention: Relaxation Response (Behavioral)

ACU+EDU

Active Comparator

acupuncture+control CD

Intervention: Acupuncture (Procedure)

SHAM+EDU

Sham Comparator

sham acupuncture+control CD

Intervention: sham acupuncture (Other)

Outcomes

Primary Outcomes

Changes in GI Symptom Per Intervention Session

Time Frame: 8 weeks

We used the GI symptom subscale of the Revised HIV Sign and Symptom Checklist (SSC-HIV) to measure the intensity (0-10) of the six targeted GI symptoms: diarrhea, loose stools, gas/bloating, abdominal pain, nausea and vomiting, with 0 indicating no symptom and 10 indicating most sever symptom. Rating changes per intervention session were estimated using a mixed effects regression model controlling for baseline ratings. Data of loose stools are presented here.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Bei-Hung Chang

Associate Professor

Boston University

Study Sites (1)

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