Effects of Reiki on Stress

Stress Clinical Trial

Official title:

Effects of Reiki on Physiological Consequences of Acute Stress

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00346671
• Other study ID #: R21AT001884-01
• Status: Completed
• Phase: Phase 1
• First received: June 29, 2006
• Last updated: September 20, 2012
• Start date: January 2006
• Est. completion date: June 2010

Study information

• Verified date: September 2012
• Source: The Cleveland Clinic
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

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.

Description:

See Brief Summary

Recruitment information / eligibility

• Status: Completed
• Enrollment: 257
• Est. completion date: June 2010
• Est. primary completion date: October 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Healthy Individuals between the age of 18 and 75

Exclusion Criteria:

• Already involved in regular (one time a week or more) mind-body practices (yoga, meditation, Qi-gong, guided imagery, Taichi, biofeedback; attendance at religious services is not considered a mind-body practice) in the past three months OR has been doing intense spiritual practice for more than 6 months in the past (an average of 6hrs a week)

• Already received an energy therapy treatment (Reiki, therapeutic touch, healing touch, touch therapy) in the past. (note: acupuncture, massage Qi-gong are not considered energy therapies in the context of this study)

• Score on the DASS21 for Depression greater or equal to 21

• Score on the DASS21 for Anxiety greater or equal to 15

• In the last 3 months, has had a major stressful life-event that is likely to affect the outcomes of the study

• Medical condition, current illness or history of chronic illness that might affect the outcomes of the study such as those affecting stress response, cardiovascular, endocrine, or immune systems (Examples: cancer, lupus, multiple sclerosis, blood-clotting disorder, severe allergies or asthma that impairs breathing, diabetes mellitus, hyperglycemia, or hypoglycemia, cardiovascular disease, depression/anxiety etc.)

• In the past 3 months, has used or is chronically using over-the-counter, recreational or prescription drugs that might affect the outcomes of the study such as those affecting cardiovascular, platelets, central nervous system, endocrine, immune systems(Examples: steroid, blood pressure medication, depression/anxiety medication, antiplatelet drugs, etc.)

• Color Blind

• Consume 3 or more alcoholic drinks per day most days over the 3 months

• Pregnant

• Problems donating blood: Fear of hypodermic needles; has felt dizzy or was about to faint following a needle stick

• Incompatibility of energy healing with religious beliefs

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Stress

Intervention

Other:
• Rest
30 min supine rest
• Sham
30 min session with Sham practitioner
• Reiki
30 min session with Reiki practitioner

Locations

Country	Name	City	State
United States	Cleveland Clinic Foundation	Cleveland	Ohio

Sponsors (2)

Lead Sponsor	Collaborator
The Cleveland Clinic	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	1: To determine whether a Reiki session affects emotional states, ANS, or HPA activity		3 years	Yes
Primary	2. To determine whether a Reiki session affects responses to a subsequent acute stressor		3 years	Yes
Secondary	Assess which benefits result from placebo and which from unique abilities of Reiki practitioners		3 years	No
Secondary	Obtain preliminary information on mechanisms needed for the rational design of a larger clinical trial		3 years	No
Secondary	Assess the role of a variety of baseline variables on responses.		3 years	Yes