Young adults' reasoning for involving a parent in a genomic decision‐making research study

Author:

Pascal Julia M.12ORCID,McGowan Michelle L.34ORCID,Blumling Amy A.1ORCID,Prows Cynthia A.15ORCID,Lipstein Ellen A.26ORCID,Myers Melanie F.12ORCID

Affiliation:

1. Division of Human Genetics Cincinnati Children's Hospital Medical Center Ohio Cincinnati USA

2. College of Medicine University of Cincinnati Cincinnati Ohio USA

3. Biomedical Ethics Research Program, Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA

4. College of Arts & Sciences University of Cincinnati Cincinnati Ohio USA

5. Division of Patient Services Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

6. James M. Anderson Center for Health Systems Excellence Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

Abstract

AbstractYoung adults have increasing genomic testing opportunities; however, little is known about how equipped they feel about making decisions to learn personal genomic information. We conducted qualitative interviews with 19 young adults, ages 18–21 years old, enrolled in a research study where they made decisions about learning personal genomic risk for developing preventable, treatable, and adult‐onset conditions and carrier status for autosomal recessive conditions. Participants had the option to include a parent in their study visit and the decision‐making process. The goal of this project was to explore young adults' reasons for involving or not involving a parent in the study and to assess young adults' perspectives about parental roles in their healthcare. Nine participants included a parent in the study and ten did not include a parent. Eleven participants received genomic test results before the interview, while eight participants had not yet received their results at the time of the interview. The study team developed a coding guide and coded interview transcripts inductively and deductively using an interpretive descriptive‐analytic approach. Logistical issues dominated solo participants' reasons for not involving a parent in the study, whereas those who involved a parent often cited a close relationship with the parent and the parent's previous involvement in the participant's healthcare as reasons for involving them. Both groups of participants described gradually transitioning to independent healthcare decision‐making with age and felt their comfort in medical decision‐making depends on the severity of and their familiarity with the situation. Participants recommended that future genomic researchers or clinicians give young adults the option to involve a parent or friend as a support person in research or clinical visits. Although young adults may have different journeys toward independent healthcare decision‐making, some may benefit from continued parental or peer involvement after reaching the age of legal adulthood.

Funder

National Human Genome Research Institute

Publisher

Wiley

Subject

Genetics (clinical)

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