Research Participation Decision-Making Among Youth and Parents of Youth With Chronic Health Conditions
UMass Chan AffiliationsGraduate School of Nursing
Document TypeJournal Article
KeywordsChronic health conditions
Health Services Administration
Health Services Research
MetadataShow full item record
AbstractThe aims of this qualitative descriptive study were to describe how past experiences with research (including communication, information, values, and support) may contribute to research fatigue among youth and parents of youth with HIV, cystic fibrosis, and Type 1 diabetes. Eighteen parents and youth were purposively recruited from outpatient subspecialty clinics at a major academic medical center. They took part in qualitative interviews and completed a demographics form and the Decisional Conflict Scale. Youth participants also completed the Erikson Psychosocial Stage Inventory. Two major themes emerged: Blurred Lines and Hope for the Future. Research fatigue was not found in this sample. Results point to challenges with informed consent in settings where research and clinical care are integrated and suggest that protective factors allow for continued participation without excess burden on youth and parents. Strategies to minimize research fatigue and support engagement in research are offered.
SourcePagano-Therrien J, Sullivan-Bolyai S. Research Participation Decision-Making Among Youth and Parents of Youth With Chronic Health Conditions. J Pediatr Health Care. 2016 Aug 20. pii: S0891-5245(16)30157-2. doi: 10.1016/j.pedhc.2016.07.002. PubMed PMID: 27553117.
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/34539
Jesica Pagano-Therrien undertook this study as a doctoral student (view her dissertation) in the Graduate School of Nursing at UMass Medical School.
Related ResourcesLink to article in PubMed