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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: REBEC
Last refreshed on: 27 May 2013
Main ID:  RBR-5dcz6y
Date of registration: 27/06/2011
Primary sponsor: FACULDADE ADVENTISTA DA BAHIA - Brazil
Public title: Religiousness and the Quality of Life of Adventists: Clinical Trial
Scientific title: Parish Nursing and Quality of Life of Adventists: Clinical Trial
Date of first enrolment: 01/05/2011
Target sample size: 180
Recruitment status: Recruitment completed
URL:  http://www.ensaiosclinicos.gov.br/rg/RBR-5dcz6y/
Study type:  Intervention
Study design:  Clinical trial preventive, randomized,single blinded, paralel with two arms and fourth phase.  
Countries of recruitment
Brazil
Contacts
Name: Gina  Abdala
Address:  Br. 101, Km.197 Cx.Postal 18 44300-000 Cachoeira Bahia Brazil
Telephone: 75-3425-8000
Email: gina.abdala@usp.br
Affiliation:  FACULDADE ADVENTISTA DA BAHIA
Name: Gina  Abdala
Address:  Br. 101, Km.197 Cx.Postal 18 44300-000 Cachoeira Bahia Brazil
Telephone: 75-3425-8000
Email: gina.abdala@usp.br
Affiliation:  FACULDADE ADVENTISTA DA BAHIA
Key inclusion & exclusion criteria
Inclusion criteria: Being a member of the Seventh Day Adventist Church, have 35 years or more. Membership in the church means to one who is christened and it regular member of the church records, which may or might not be frequenting weekly.
Exclusion criteria: To refuse to participate in this study.

Age minimum: 35Y
Age maximum: 100Y
Gender: -
Health Condition(s) or Problem(s) studied
Quality of life, religion, spirituality, elderly.
I01.800
K01.844
M01.060.116.100
F02.880.705
Intervention(s)
Religious intervention: the group will be divided in experimental (Group 1- 90 members) and control group (Group 2 - 90 members). The intervention will be through home visitation to the experimental group encouraging them to attend the church (at least once/week), praying 3 times per day and reading the Bible (at least 1 chapter per day). This intervention will take place for four months. The Group 2 will not receive any intervention. The questionaries of Religion Index Scale (Duke-Durel) and Short-Form SF36 Health Survey will be used on this research.
Primary Outcome(s)
Those who have received at the beginning scores less than 50 on the SF 36 will have the intervention (experimental group) and this test will take place on the end of the study in order to have a comparisson with control group too.
Secondary Outcome(s)
From this result, the study group will check if the quality of life of the church members would increase from the influence of increased religiosity.
Secondary ID(s)
Nº 0057.0.070.000-11
Nº 029/11
Source(s) of Monetary Support
FACULDADE ADVENTISTA DA BAHIA - Brazil
Secondary Sponsor(s)
Gina Andrade Abdala - Brazil
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