Complementary therapies such as Reiki are becoming popular. Reiki is a practice used for relaxation and pain management that involves physical touch and social contact with a trained, empathetic practitioner. Unlike many relaxation therapies, Reiki requires no participation by the patient, a feature that makes Reiki particularly attractive in the hospital setting, where patients are often extremely anxious, depressed, in pain, or sedated. Our primary research questions are to determine whether physiological changes are induced during a Reiki session and whether a Reiki session affects responses to a subsequent acute stressor. Secondary research questions include assessing which benefits result from placebo or unique abilities of "attuned" Reiki practitioners and assessing background characteristics of recipients that are associated with acceptance and responsiveness. Based on its use to reduce pain and anxiety, we will study potential mechanisms by which Reiki decreases activity of the sympathetic nervous system and other stress pathways. Comparison of the responses in a Reiki group with those in supine-control and sham groups will allow us to gain insights into mechanisms by which Reiki effects are mediated. Information obtained from the proposed studies will provide detailed information on physiological pathways affected by Reiki. Should Reiki decrease stress pathways or reduce physiological responses to stressful situations, it could be a useful adjunct to traditional medicine and have significant health and economic benefits.
See Brief Summary
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
257
Cleveland Clinic Foundation
Cleveland, Ohio, United States
1: To determine whether a Reiki session affects emotional states, ANS, or HPA activity
Time frame: 3 years
2. To determine whether a Reiki session affects responses to a subsequent acute stressor
Time frame: 3 years
Assess which benefits result from placebo and which from unique abilities of Reiki practitioners
Time frame: 3 years
Obtain preliminary information on mechanisms needed for the rational design of a larger clinical trial
Time frame: 3 years
Assess the role of a variety of baseline variables on responses.
Time frame: 3 years
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