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Distant Healing for HIV/AIDS

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00079534
First Posted: March 10, 2004
Last Update Posted: August 18, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
National Center for Complementary and Integrative Health (NCCIH)
March 9, 2004
March 10, 2004
August 18, 2006
December 2000
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Complete list of historical versions of study NCT00079534 on ClinicalTrials.gov Archive Site
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Distant Healing for HIV/AIDS
Distant Healing Efforts for AIDS by Nurses and "Healers"
The purpose of this study is to determine whether individuals praying at a distance (also known as "Distant Healing") can positively affect the health of people with HIV/AIDS.

Significant numbers of people with HIV/AIDS seek spiritual or “psychic" treatment. Distant healing could potentially be of benefit to large numbers of HIV/AIDS patients, as it is widely available and requires no travel or other activity on the part of the patient. However, the treatment can be costly and has not yet been proven effective in a controlled clinical trial. This study will evaluate the efficacy of distant healing in patients with HIV/AIDS.

Participants in this study will be randomly assigned to either the distant healing group or a control group. All participants will have hour-long study visits at entry and Months 6 and 12. At study visits, participants will complete a demographic questionnaire, self-report health and symptom inventory, quality of life assessment, and profile of mood states. Blood will be drawn at each study visit.

Interventional
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Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
  • HIV Infections
  • AIDS
Behavioral: Non-local/distant healing or prayer
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
150
December 2003
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Inclusion criteria

  • HIV infection
  • History of a CD4 cell count less than 200 cells/mm3
  • Stable antiretroviral regimen
  • English-speaking

Exclusion criteria

  • Inability or unwillingness to fill out questionnaires
  • History of non-HIV related life-threatening disease
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00079534
R01AT000485-01( U.S. NIH Grant/Contract )
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National Center for Complementary and Integrative Health (NCCIH)
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Principal Investigator: Donald Abrams, MD University of California, San Francisco
Study Director: Jerome J. Stone, MA, RN California Pacific Medical Center
National Center for Complementary and Integrative Health (NCCIH)
August 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP