Effects of Remote Intercessory Prayer

This study has been completed.
Sponsor:
Information provided by:
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude
ClinicalTrials.gov Identifier:
NCT01053780
First received: January 19, 2010
Last updated: January 20, 2010
Last verified: October 2009
  Purpose

Intercessory prayer can improve the outcome of pregnancies?


Condition Intervention
Remote Intercessory Prayer
Other: Intercessory Prayer
Behavioral: Intercessory Prayer

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effects of Remote Intercessory Prayer in Outcomes of Pregnants Women: a Randomized Controlled Trial

Further study details as provided by Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude:

Primary Outcome Measures:
  • Apgar score [ Time Frame: birth . The time to collect the outcome must be at least the tenth day after making randomization. If the birth occurs before the patient will be excluded from the study. ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • type of delivery complications in childbirth [ Time Frame: birth or abortion. There isn't a pre-determined time. Must be at least 9 days after randomization to allow time to be done the intervention (intercessory prayer) ] [ Designated as safety issue: Yes ]

Enrollment: 565
Study Start Date: August 2008
Study Completion Date: January 2010
Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: Intercessory Prayer
    A committed group of six people selected by the chief investigator prayed nine consecutive days for the patients in the intervention group; they were blind to the identity , the patients' first name, were given to the intercessors.
    Behavioral: Intercessory Prayer
    A committed group of six people selected by the chief investigator prayed nine consecutive days for the patients in the intervention group; they were blind to the identity , the patients' first name, were given to the intercessors.
  Eligibility

Ages Eligible for Study:   15 Years to 45 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • be pregnant, belong to the public health system

Exclusion Criteria:

  • no consent to participate in the research
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01053780

Locations
Brazil
Maria Inês da Rosa
Criciúma, Santa Catarina, Brazil, 88811-550
Universidade do Extremo Sul catarinense
Criciúma, Santa Catarina, Brazil
Universidade do Extremo Sul Catarinense
Criciuma, SC, Brazil
Sponsors and Collaborators
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT01053780     History of Changes
Other Study ID Numbers: UNESC
Study First Received: January 19, 2010
Last Updated: January 20, 2010
Health Authority: Brazil: National Information System on Research Ethics

Keywords provided by Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude:
Intercessory Prayer, pregnants

ClinicalTrials.gov processed this record on July 23, 2014