ArticleJournal of medical Internet research2013
Online information exchanges for parents of children with a rare health condition: key findings from an online support community.
Article in Journal of medical Internet research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
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Who cites it
24 citing papers in PubMed.
- Online Questions About Clubfoot Surgery: Content Analysis and Development of a Patient Education Resource.Journal of the Pediatric Orthopaedic Society of North America · 2026Article
- Social Media Use Among Parents and Caregivers of Children With Rare Genetic Diseases: Scoping Review.Journal of medical Internet research · 2025Article
- Understanding the Real Needs and Expectations of French Patients with Amelogenesis Imperfecta Through Facebook Content: A Qualitative Thematic Analysis.Healthcare (Basel, Switzerland) · 2025Article
- Online Support Groups for Family Caregivers: Scoping Review.Journal of medical Internet research · 2023Article
- Diagnosis Disclosure and Peer-to-Peer Information Seeking Among COVID-19-Infected Social Media Users: Survey of US-Based Adults.JMIR formative research · 2023Article
- Spontaneously generated online patient experience data - how and why is it being used in health research: an umbrella scoping review.BMC medical research methodology · 2022Article
- Facebook Support Groups for Pediatric Rare Diseases: Cross-Sectional Study to Investigate Opportunities, Limitations, and Privacy Concerns.JMIR pediatrics and parenting · 2022Article
- Spontaneously Generated Online Patient Experience of Modafinil: A Qualitative and NLP Analysis.Frontiers in digital health · 2021Article
- Facebook Support Groups for Rare Pediatric Diseases: Quantitative Analysis.JMIR pediatrics and parenting · 2020Article
- Availability and Quality of Web Resources for Parents of Children With Disability: Content Analysis and Usability Study.JMIR pediatrics and parenting · 2020Article
- Co-creating a knowledge base in the "22q11.2 deletion syndrome" community.Journal of community genetics · 2020Article
- Liberating parents from guilt: a grounded theory study of parents' internet communities for the recognition of ADHD.International journal of qualitative studies on health and well-being · 2019Article
- Internet Use by Parents of Children With Rare Conditions: Findings From a Study on Parents' Web Information Needs.Journal of medical Internet research · 2017Article
- The Role of Online Social Support in Supporting and Educating Parents of Young Children With Special Health Care Needs in the United States: A Scoping Review.Journal of medical Internet research · 2016Article
- Health-Related Internet Use by Informal Caregivers of Children and Adolescents: An Integrative Literature Review.Journal of medical Internet research · 2016Review
- VisOHC: Designing Visual Analytics for Online Health Communities.IEEE transactions on visualization and computer graphics · 2016Article
- An exploration of information exchange by adolescents and parents participating in adolescent idiopathic scoliosis online support groups.Scoliosis and spinal disorders · 2016Article
- Using the internet to seek information about genetic and rare diseases: a case study comparing data from 2006 and 2011.JMIR research protocols · 2014Article
- Community management that works: how to build and sustain a thriving online health community.Journal of medical Internet research · 2013Article
- The internet user profile of Italian families of patients with rare diseases: a web survey.Orphanet journal of rare diseases · 2013Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe Internet provides new opportunities for parents of children with difficult illnesses and disabilities to find information and support. The Internet is particularly important for caregivers of children with special needs due to numerous health-related decisions they face. For at-risk populations, online support communities can become key settings and channels for health promotion and communication.
objectiveThis study is an initial exploration of the information-seeking and information-provision processes present in an online support community, which is an area of opportunity and interest for Internet-based medical research and practice. The aim of this study was to explore and describe information-related processes of uncertainty management in relationship to clubfoot. Specifically, the study explored interpersonal communication (information seeking and provision) in an online support community serving the needs of parents of children with clubfoot.
methodsThe study population consisted of messages posted to an online community by caregivers (parents) of children with clubfoot. The theoretical framework informing the study was the Uncertainty Management Theory (UMT). The study used content analysis to explore and categorize the content of 775 messages.
resultsWomen authored 664 of 775 messages (86%) and men authored 47 messages (6%). Caregivers managed uncertainty through information seeking and provision behaviors that were dynamic and multilayered. The ratio of information-seeking messages to information-provision responses was 1 to 4. All five types of information-seeking behaviors proposed by Brashers' schema were identified, most of them being correlated. Information seeking using direct questions was found to be positively correlated to self-disclosure (r=.538), offering of a candidate answer (r=.318), and passive information seeking (r=.253). Self-disclosure was found to be positively correlated to provision of a candidate answer (r=.324), second-guessing (r=.149), and passive information seeking (r=.366). Provision of a candidate answer was found to be positively correlated with second-guessing (r=.193) and passive information seeking (r=.223). Second-guessing was found to be positively correlated to passive information seeking (r=.311). All correlations reported above were statistically significant (P<0.01). Of the 775 messages analyzed, 255 (33%) identified a medical professional or institution by name. Detailed medical information was provided in 101 (13%) messages, with the main source of information identified being personal experience rather than medical sources.
conclusionOnline communities can be an effective channel for caregivers, especially women, to seek and offer information required for managing clubfoot-related uncertainty. To enhance communication with parents, health care institutions may need to invest additional resources in user-friendly online information sources and online interactions with caregivers of children with special illnesses such as clubfoot. Furthermore, explorations of information-seeking and information-provision behaviors in online communities can provide valuable data for interdisciplinary health research and practice.
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