Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Nov;81(11):713-20.
doi: 10.1111/j.1746-1561.2011.00648.x.

Associations between academic achievement and psychosocial variables in adolescents with cystic fibrosis

Affiliations

Associations between academic achievement and psychosocial variables in adolescents with cystic fibrosis

Adam J Grieve et al. J Sch Health. 2011 Nov.

Abstract

Background: Cystic fibrosis (CF) is a chronic genetic disease that leads to the accumulation of thick mucus in multiple organ systems, leading to chronic lung infection and affecting the body's ability to absorb nutrients necessary for growth and development. This cross-sectional, correlational study examined the potential effects of CF on students' psychosocial and academic development.

Methods: Forty adolescents with CF completed a battery of neuropsychological and psychosocial measures. Their school records were reviewed to abstract information about standardized achievement testing results and grade point average (GPA). Academic outcomes were hypothesized to be associated with (1) self-efficacy, (2) disease and school-specific coping strategies, (3) attitude to school, and (4) depression.

Results: Cognitive and academic scores were within the normal range, and self-efficacy had the strongest association with standardized cognitive and academic measures and high school grades. School absences were associated with GPA, but not standardized test scores.

Conclusion: Adolescents with CF require supports in school that foster their sense of self-efficacy and accommodations that address the learning time lost from extended health-related absences.

PubMed Disclaimer

Similar articles

Cited by

References

    1. O’Sullivan BP, Freedman SD. Cystic fibrosis. Lancet. 2009;373:1891–1904. - PubMed
    1. Cystic Fibrosis Foundation. About Cystic Fibrosis. Available at http://www.cff.org/AboutCF/ Accessed June 3, 2010.
    1. Osman LP, Roughton M, Hodson ME, Pryor JA. Short-term comparative study of high frequency chest wall oscillation and European airway clearance techniques in patients with cystic fibrosis. Thorax. 2010;65:196–200. - PMC - PubMed
    1. Borowitz D, Baker RD, Stallings VA. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr. 2002;35:246–259. - PubMed
    1. Cystic Fibrosis Foundation. Patient registry 2006 annual report. Bethesda, MD: Cystic Fibrosis Foundation; 2008.

Publication types