Objective: We aim to understand the association between father involvement in middle childhood and adolescent behaviors and whether the relationship differs by father residence.
Background: Internalizing and externalizing behaviors in adolescence can trigger a cascade of negative outcomes later in life, including lower educational attainment, criminal justice involvement, and future psychological distress. Evidence, largely focusing on nonresidential fathers and older cohort, suggests that father involvement-particularly closeness and engagement-may reduce adolescents' internalizing and externalizing behaviors.
Method: We use data six waves of the Fragile Families and Child Wellbeing Study, a birth cohort survey representative of births in large U.S. cities between 1998 and 2000, to estimate OLS regression models examining (a) whether father involvement in middle childhood is associated with fewer problem behaviors at Age 15, (b) if the salience of father involvement differs depending on whether the father was present in the home (i.e., was married to or living with his child's mother) in middle childhood, and (c) whether father involvement matters differently based on the child's sex.
Results: We find protective associations between father involvement and adolescent behavioural outcomes that persist even among children who were not living with their fathers. In models stratified by the child's sex, father involvement matters for both boys and girls. In all models, father presence alone, apart from active involvement, is not significantly associated with behavioral outcomes.
Conclusion: Father involvement protects against negative adolescent behaviors even among children with nonresidential fathers and for both boys and girls.
Implications: These results suggest that policies that promote greater father involvement and father-child bonds, rather than other options such as promoting marriage, may be more effective in reducing behavioral problems among adolescents.
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http://dx.doi.org/10.1111/jomf.12676 | DOI Listing |
PLoS One
January 2025
School of Public Health, University of Memphis, Memphis, Tennessee, United States of America.
Female Genital Mutilation (FGM) has become a global health concern. It is a deeply entrenched harmful practice involving partial or total removal of the external female genitalia for non-medical reasons. To inform effective policymaking and raise awareness about FGM's health risks, understanding socioeconomic and demographic factors influencing the timing of girls' circumcision is crucial.
View Article and Find Full Text PDFJ Res Adolesc
March 2025
Department of Psychology, University of Notre Dame, Notre Dame, Indiana, USA.
Families manage daily conflict through communication and healthy family communication is critical to promoting better family relationships and youth adjustment. Community families without high-risk factors, such as domestic dispute or clinical problems, are no less affected by the ramifications of poor communication and conflict management. However, there is limited translational research on community families analyzing the changes in parent-adolescent communication quality.
View Article and Find Full Text PDFBehav Sci (Basel)
December 2024
Public Health & Anthropology, Syracuse University, Syracuse, NY 13244, USA.
This article focuses on the impact of trauma experienced by individuals, families and groups, and neighborhoods in Rochester and Syracuse, New York. Using the levels of analysis put forward in Bronfenbrenner's ecological systems theory (i.e.
View Article and Find Full Text PDFFront Genet
January 2025
Genetics and Precision Medical Center, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Introduction: Mucopolysaccharidosis type VI (MPSVI), an autosomal recessive lysosomal storage disorder caused by pathogenic variants in gene. Usually, whole exome sequencing (WES) can identify these variants, and if WES failed to detect causative variants, whole-genome sequencing (WGS) may be considered to investigate deep intronic variations and structural alterations in patients.
Methods: Whole-exome sequencing (WES) and whole genome sequencing (WGS) were performed in a Chinese family having a boy with suspected diagnosis of MPS with macrocephaly, coarse facial features, broad forehead, thick lips, frontal bossing, craniosynostosis, blue spots, frequent upper respiratory infections, inguinal hernia, and dysostosis multiplex.
World J Mens Health
January 2025
Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Purpose: In recent years, many genes have been associated with male infertility; however, testing of monogenic forms has not yet been clinically implemented in the diagnosis of severe forms of idiopathic male infertility, as the diagnostic utility has not been established yet. The aim of this study was therefore to answer if the implementation of genetic testing for monogenic forms of male infertility could contribute to the clinical diagnosis of men with severe forms of idiopathic male infertility.
Materials And Methods: Based on the ClinGene curation protocol, we defined a panel of genes with sufficient evidence for the involvement with severe male infertility.
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