Study of the Therapeutic Effects of Intercessory Prayer (STEP) - Full Text View

Sponsor:	Beth Israel Deaconess Medical Center
Collaborators:	John Templeton Foundation Mind/Body Medical Institute INTEGRIS Baptist Medical Center Washington Hospital Center Baptist Memorial Health Care Corporation Mayo Clinic
Information provided by:	Beth Israel Deaconess Medical Center
ClinicalTrials.gov Identifier:	NCT00179491

Purpose

Intercessory prayer is widely believed to influence recovery from illness, but claims of benefits are not supported by well-controlled clinical trials. Prior studies have not addressed whether prayer itself or knowledge/certainty that prayer is being provided may influence outcome. We evaluated whether (1) receiving intercessory prayer or (2) being certain of receiving intercessory prayer was associated with uncomplicated recovery after coronary artery bypass graft (CABG) surgery.

Condition	Intervention	Phase
Coronary Artery Bypass Grafting Surgery	Behavioral: Intercessory Prayer	Phase III

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title:	Study of the Therapeutic Effects of Intercessory Prayer (STEP)

Resource links provided by NLM:

MedlinePlus related topics: Coronary Artery Bypass Surgery Surgery

U.S. FDA Resources

Further study details as provided by Beth Israel Deaconess Medical Center:

Primary Outcome Measures:

Whether receiving intercessory prayer was associated with uncomplicated recovery after coronary artery bypass graft (CABG) surgery. [ Time Frame: 30 days ]

Secondary Outcome Measures:

Whether being certain of receiving intercessory prayer was associated with uncomplicated recovery after coronary artery bypass graft (CABG) surgery. [ Time Frame: 30 days ]

Enrollment:	1802
Study Start Date:	April 1998
Study Completion Date:	November 2001

Arms	Assigned Interventions
Group 1: Active Comparator 604 patients received intercessory prayer after being informed they may or may not receive prayers (Group 1)	Behavioral: Intercessory Prayer 14 days of intercessory prayer from 3 sites
2: No Intervention 597 patients did not receive prayer after being informed they may or may not receive prayer (Group 2)
Group 3: Experimental 601 patients received intercessory prayer after being informed they would receive it (Group 3).	Behavioral: Intercessory Prayer 14 days of intercessory prayer from 3 sites

Detailed Description:

Intercessory prayer is widely believed to influence recovery from illness, but claims of benefits are not supported by well-controlled clinical trials. Prior studies have not addressed whether prayer itself or knowledge/certainty that prayer is being provided may influence outcome. We evaluated whether (1) receiving intercessory prayer or (2) being certain of receiving intercessory prayer was associated with uncomplicated recovery after coronary artery bypass graft (CABG) surgery.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion criteria:

Age 18 years or older
Able to read or understand English

Exclusion criteria:

Scheduled for emergent CABG (next available operating room slot)
CABG more than 14 days after enrollment
Other planned surgery within 30 days of CABG
Minimally invasive CABG (non full sternotomy incisions)
CABG with planned valve replacement, stent, angioplasty or carotid endarterectomy
Or had ongoing chest pain or unstable angina, as defined by their physicians

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00179491

Sponsors and Collaborators

Beth Israel Deaconess Medical Center

John Templeton Foundation

Mind/Body Medical Institute

INTEGRIS Baptist Medical Center

Washington Hospital Center

Baptist Memorial Health Care Corporation

Mayo Clinic

Investigators

Principal Investigator:

Herbert Benson, MD

Beth Israel Deaconess Medical Center, Mind/Body Medical Institute

More Information

No publications provided

Study ID Numbers:	2001-P-002125
Study First Received:	September 13, 2005
Last Updated:	November 2, 2007
ClinicalTrials.gov Identifier:	NCT00179491 History of Changes
Health Authority:	United States: Food and Drug Administration

Keywords provided by Beth Israel Deaconess Medical Center:

coronary artery bypass grafting surgery

ClinicalTrials.gov processed this record on November 20, 2009