Other search tools

About this data

The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

If you have any questions or comments, please contact us.

Results: 1 to 6 of 6

Publication Record

Connections

The role of community psychology in Christian community development.
Eccleston SMP, Perkins DD
(2019) J Community Psychol 47: 291-310
MeSH Terms: Adult, Christianity, Community Networks, Empowerment, Humans, Psychology, Qualitative Research, Social Behavior, Social Participation, Social Planning
Show Abstract · Added February 8, 2020
This project examines the connections between community psychology and faith-based community development. We investigate whether and how 4 major principles of community psychology-neighboring, sense of community, empowerment, and citizen participation-are found in the theory and philosophy of practice of the Christian Community Development Association (CCDA), a national faith-based community development network. We employ content analysis of four official CCDA publications to identify whether and how these four principles are embedded in the organization's espoused principles of practice. Our findings are as follows: (a) All four principles are found within CCDA theory and philosophy of practice, with the greatest emphasis on neighboring and sense of community and a less robust application of empowerment and citizen participation; (b) CCDA primarily focuses on the individual-level impact of these principles; and (c) CCDA Bases their application of these principles in Christian scripture and tradition. Our results indicate that the field could be strengthened by examining religious approaches to these principles and considering how organizations engage these concepts in both the theory and the practice. Additionally, faith-based organizations may foster a more effective application of these concepts in their social change efforts by partnering with community researchers and practitioners.
© 2018 Wiley Periodicals, Inc.
0 Communities
1 Members
0 Resources
10 MeSH Terms
Discussing adolescent sexual health in African-American churches.
Williams TT, Dodd D, Campbell B, Pichon LC, Griffith DM
(2014) J Relig Health 53: 339-51
MeSH Terms: Adolescent, Adolescent Behavior, Adult, African Americans, Attitude to Health, Child, Christianity, Clergy, Female, Focus Groups, Health Behavior, Health Promotion, Humans, Interviews as Topic, Male, Michigan, Middle Aged, Religion and Psychology, Reproductive Health, Sex Education, Sexual Behavior
Show Abstract · Added March 27, 2014
This study describes the ways in which two African-American churches discuss adolescent sexual health topics. Six focus groups were conducted in two churches in Flint, Michigan, that reported no formal sexual health programming for their congregants. Three themes emerged to highlight the different perspectives about the role of churches in adolescent sexual decision-making and sexual health education: (1) churches as sources of sexual information, (2) churches as complex communities, and (3) recommendations for sexual education in churches. Participant responses suggest that churches can and should serve a resource for sexual health information. Implications for practice and research are discussed.
0 Communities
1 Members
0 Resources
21 MeSH Terms
The Sickle Cell Sabbath: a community program increases first-time blood donors in the African American faith community.
Price CL, Johnson MT, Lindsay T, Dalton D, Watkins AR, DeBaun MR
(2009) Transfusion 49: 519-23
MeSH Terms: Adolescent, Adult, African Americans, Aged, Aged, 80 and over, Anemia, Sickle Cell, Blood Donors, Christianity, Community Health Services, Female, Health Education, Humans, Male, Middle Aged
Show Abstract · Added November 27, 2013
BACKGROUND - Blood transfusion therapy is an established treatment for primary and secondary prevention of strokes in children with sickle cell disease (SCD), a disease that predominantly affects African Americans. African American blood donors are more likely to have compatible minor red blood cell antigens for children with SCD who routinely receive transfusions. This study tested the hypothesis that when informed at church about the importance of blood donation, African Americans will have a higher than expected rate of first-time blood donation compared to the general population.
STUDY DESIGN AND METHODS - The Sickle Cell Sabbath Program was developed to increase awareness about SCD and the importance of blood donations within the African American faith community. Church involvement in the program included a 5-minute scripted educational session about SCD that included the importance of blood donations followed by a blood donor drive that was hosted by the church.
RESULTS - Thirteen African American churches sponsored 34 blood drives from 2003 through 2006. Each church sponsored at least two blood drives. Approximately 1200 donors participated in the sickle cell blood drives. The majority of the donors were first-time donors and represented a greater than expected first-time donor rate when compared to first-time donors in the metropolitan St Louis area, 60 percent (422 of 699) and 12.2 percent (21,516 of 175,818), respectively (p = 0.001).
CONCLUSION - An educational program that engages the African American faith community more than quadruples the rate of expected first-time blood donors when compared to the general community over this 4-year period.
1 Communities
1 Members
0 Resources
14 MeSH Terms
The importance of genealogy in determining genetic associations with complex traits.
Newman DL, Abney M, McPeek MS, Ober C, Cox NJ
(2001) Am J Hum Genet 69: 1146-8
MeSH Terms: Artifacts, Christianity, Chromosome Mapping, Consanguinity, Founder Effect, Genetic Linkage, Humans, Multifactorial Inheritance, Pedigree, Polymorphism, Genetic, Quantitative Trait, Heritable, Research Design
Added February 22, 2016
0 Communities
1 Members
0 Resources
12 MeSH Terms
Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
Ober C, Leavitt SA, Tsalenko A, Howard TD, Hoki DM, Daniel R, Newman DL, Wu X, Parry R, Lester LA, Solway J, Blumenthal M, King RA, Xu J, Meyers DA, Bleecker ER, Cox NJ
(2000) Am J Hum Genet 66: 517-26
MeSH Terms: Alleles, Asthma, Child, Christianity, Chromosomes, Human, Pair 16, DNA Mutational Analysis, Ethnic Groups, Family Health, Female, Gene Frequency, Genetic Predisposition to Disease, Genetic Variation, Haplotypes, Humans, Hypersensitivity, Immediate, Linkage Disequilibrium, Male, Molecular Sequence Data, Phenotype, Polymorphism, Single Nucleotide, Receptors, Interleukin-4, United States
Show Abstract · Added February 22, 2016
After a genomewide screen in the Hutterites was completed, the IL4RA gene was examined as the 16p-linked susceptibility locus for asthma and atopy. Seven known variants and one novel variant, representing all nonsynonymous substitutions in the mature protein, were examined in the Hutterites; on the basis of studies in the Hutterites, outbred white, black, and Hispanic families were genotyped for selected markers. All population samples showed evidence of association to atopy or to asthma (P values.039-.0044 for atopy and. 029-.0000061 for asthma), but the alleles or haplotypes showing the strongest evidence differed between the groups. Overall, these data suggest that the IL4RA gene is an atopy- and asthma-susceptibility locus but that variation outside the coding region of the gene influences susceptibility.
0 Communities
1 Members
0 Resources
22 MeSH Terms
Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.
Pannain S, Weiss RE, Jackson CE, Dian D, Beck JC, Sheffield VC, Cox N, Refetoff S
(1999) J Clin Endocrinol Metab 84: 1061-71
MeSH Terms: Child, Preschool, Christianity, Chromosome Mapping, Congenital Hypothyroidism, Consanguinity, Ethnic Groups, Female, Genetic Linkage, Goiter, Haplotypes, Homozygote, Humans, Hypothyroidism, Intellectual Disability, Iodide Peroxidase, Male, Mutation, Pedigree, Phenotype
Show Abstract · Added February 22, 2016
Approximately 10% of newborns with congenital hypothyroidism are unable to convert iodide into organic iodine. This iodide organification defect has a prevalence of 1 in 40,000 newborns and may be caused by defects in the thyroid peroxidase enzyme (TPO), the hydrogen peroxide-generating system, the TPO substrate thyroglobulin, or inhibitors of TPO. We identified a high incidence of severe hypothyroidism due to a complete iodide organification defect in the youngest generation of five nuclear families belonging to an inbred Amish kindred. Genealogical records permitted us to trace their origin to an ancestral couple 7-8 generations back and to identify an autosomal recessive pattern of inheritance. Initial studies of homozygosity by descent using two polymorphic markers within the TPO gene showed no linkage to the phenotype. In fact, 4 of 15 affected siblings from 2 of the nuclear families were heterozygous, resulting in homozygosity values of 73% and 53% in affected and unaffected family members, respectively. A genome-wide homozygosity screen using DNA pools from affected and unaffected family members localized the defect to a locus close to the TPO gene. Linkage analysis using 4 additional polymorphic markers within the TPO gene reduced the number of homozygous unaffected siblings to zero without altering the percent homozygosity initially found in the affected. Sequencing of the TPO gene revealed 2 missense mutations, E799K and R648Q. TPO 779K was found in both alleles of the 11 affected homozygotes, both mutations were present in each of the 3 affected compound heterozygotes, and there were no TPO mutations in 1 subject with hypothyroidism of different etiology. These results demonstrate the power of the DNA pooling strategy in the localization of a defective gene and the pitfalls of linkage analysis when 2 relatively rare mutations coexist in an inbred population.
0 Communities
1 Members
0 Resources
19 MeSH Terms