Evidence map›Paper›PMID 28246072›Full record

ArticleJournal of medical Internet research2017

Internet Use by Parents of Children With Rare Conditions: Findings From a Study on Parents' Web Information Needs.

Honor Nicholl, Catherine Tracey, Thelma Begley, Carole King, Aileen M Lynch

Abstract read
In one paragraph

Article in Journal of medical Internet research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  10. Identifying the Impacts, Obstacles and Information Barriers for Parents of Children Living With Genetic Neurodevelopmental Disorders: A Qualitative Study.Health expectations : an international journal of public participation in health care and health policy · 2025
    Observational
  11. Article
  12. Content Analysis of a Congenital Cataract Social Media Support Group.Clinical ophthalmology (Auckland, N.Z.) · 2025
    Article
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  15. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Honor NichollSchool of Nursing and Midwifery, Trinity College Dublin, the University of Dublin, Dublin, Ireland.ORCID 0000-0003-3589-1766
Catherine TraceySchool of Nursing and Midwifery, Trinity College Dublin, the University of Dublin, Dublin, Ireland.ORCID 0000-0001-5398-6924
Thelma BegleySchool of Nursing and Midwifery, Trinity College Dublin, the University of Dublin, Dublin, Ireland.ORCID 0000-0001-7090-6367
Carole KingSchool of Nursing and Midwifery, Trinity College Dublin, the University of Dublin, Dublin, Ireland.ORCID 0000-0003-2029-1143
Aileen M LynchSchool of Nursing and Midwifery, Trinity College Dublin, the University of Dublin, Dublin, Ireland.ORCID 0000-0001-9982-7697

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParents of children with rare conditions increasingly use the Internet to source information on their child's condition. This study reports on part of a larger study whose overall aim was to identify the Internet use by parents when seeking information on their child's rare condition, with the specific purpose of using the findings to aid in the development of a website specifically designed to meet the parents' needs. It presents findings on why these parents use the Internet, the information and support content they source, and the impact these resources have on their capacity to care for and manage their child's condition.

objectiveTo (1) ascertain parents' general Internet usage patterns, (2) identify the nature of the information parents most frequently searched for, and (3) determine the effect the Internet-sourced information had on parents of children with rare conditions.

methodsData collection was conducted in 2 parts: Part 1 was a focus group interview (n=8) to inform the development of the questionnaire, and Part 2 was a questionnaire (Web- and paper-based). All respondents (N=128) completed the questionnaire using the Internet.

resultsParents frequently and habitually used the Internet and social media to gather information on their child's condition. These Web-based resources provide parents with a parent-to-parent support platform that allows them to share their experiences and information with other parents, which, the respondents considered, improved their knowledge and understanding of their child's condition. The respondents also reported that these resources positively impacted on their decision making, care, and management of their child's condition. However, they reported receiving mixed responses when wishing to engage and share with health care professionals their Internet and social media interactions and information outcomes.

conclusionsThis study adds to the emerging body of research on the Internet use by parents of children with rare conditions to source information on their child's condition. The evolving and ever increasing parent-to-parent support systems via social media are impacting on parents' capacity to manage their children. Implications for practice include health care professionals' response to this knowledge and capacity shift, and the significance of these changes when interacting with parents. The key message of this study was that parents of children with rare conditions are habitual users of the Internet to source information about their children's conditions. Social media, especially Facebook, has an increasing role in the lives of these parents for information and support. Parents' interest in information gathering and sharing includes a desire for shared dialogue with health care professionals.

Indexed as

AdolescentAdultChildChild, PreschoolDecision MakingFemaleHealth Information ExchangeHumansInternetMaleParentsPhysician-Patient RelationsRare DiseasesSurveys and QuestionnairesYoung Adultconsumer health informationInternetparentsprofessional-patient relationsrare diseasessocial media

Identifiers

PMID28246072
PMCPMC5350458

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.