Children's at Home: Pilot Study Assessing Dedicated Social Media for Parents of Adolescents with Neurofibromatosis Type 1.

TitreChildren's at Home: Pilot Study Assessing Dedicated Social Media for Parents of Adolescents with Neurofibromatosis Type 1.
Publication TypeJournal Article
Year of Publication2018
AuthorsAkré, C, Polvinen, J, Ullrich, NJ, Rich, M
JournalJournal of genetic counseling
Volume27
Issue2
Pagination505-517
Date Published04/2018
DOI10.1007/s10897-018-0213-0
ISSN1573-3599
Mots-clésAdolescent, Adolescents, Child, Female, Humans, Intervention, Male, Neurofibromatosis, Neurofibromatosis 1/psychology, Parents, Parents/psychology, Peer support, Pilot Projects, Social media
Abstract

The aim of this pilot study was to evaluate Children's at Home (C@H), a dedicated social media website for parents of adolescents with neurofibromatosis type 1 (NF1). The interventional study included two phases: (1) creating video intervention/prevention assessment (VIA) visual narratives about having an adolescent with NF1 and (2) interacting on C@H, a secure, medically moderated social media website. C@H was evaluated qualitatively at three time points. At enrollment (T0, N = 17), participants reported needing C@H to break their isolation, connect with other families, and receive accurate information, advice, and support from others facing similar challenges. At T1, after creating VIA during 6 months (N = 13, 145 videos), participants mostly valued the opportunity to speak about the challenges they face with NF1 and their journey since diagnosis. At T2, after interacting on C@H for 7 weeks (N = 10, two sign-ins/week/parent), participants reported connecting with other parents of children with NF1 for the first time, valuing the "real faces" and emotions of other parents with shared experiences providing a sense of normalcy. Qualitative analysis suggested that C@H decreased feelings of isolation, provided relief to talk about NF1 without having to explain it, provided new knowledge about NF1 and the opportunity to address non-medical issues of NF1 never discussed in clinic, and helped participants with putting their lives into perspective. C@H allowed parents of adolescents with NF1 to overcome previous isolation and connect for the first time. Innovative applications of social media dedicated to those who care for children with chronic conditions can provide peer-to-peer support, shared experience, and reliable medical information.

Alternate URL

http://www.ncbi.nlm.nih.gov/pubmed/29383545?dopt=Abstract

First publication date (online)

01/2018

WOS ID (UT)

000427926900021

Alternate JournalJ Genet Couns
Citation Key / SERVAL ID8570
Peer reviewRefereed
PubMed ID29383545
Grant ListClinical Research Award / / Children's Tumor Foundation / United States
P1LAP3_151749 / / Swiss National Science Foundation / United States
                         

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