Availability and Quality of Web Resources for Parents of Children With Disability: Content Analysis and Usability Study

被引:5
作者
Buteau-Poulin, Anabel [1 ]
Gosselin, Camille [1 ]
Bergeron-Ouellet, Andrea [1 ]
Kiss, Jocelyne [2 ]
Lamontagne, Marie-Eve [1 ]
Maltais, Desiree [1 ]
Trottier, Christiane [3 ]
Desmarais, Chantal [1 ]
机构
[1] Univ Laval, Rehabil Dept, 2325 Rue Univ, Quebec City, PQ G1V 0A6, Canada
[2] Univ Laval, Mus Dept, Quebec City, PQ, Canada
[3] Univ Laval, Phys Educ Dept, Quebec City, PQ, Canada
来源
JMIR PEDIATRICS AND PARENTING | 2020年 / 3卷 / 02期
关键词
disabled child; parents; health knowledge; internet-based intervention; validation study; EMOTIONAL SUPPORT; FAMILY NEEDS; INFORMATION; UNDERSTANDABILITY;
D O I
10.2196/19669
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: The internet is a valuable resource for parents of typical children, who are looking for information about their children's growth and development and how to boost them. However, for parents of children with special needs, especially for non-English-speaking parents, there are anecdotal reports stating that specific and accurate information is not available on the internet. Objective: This study aims to describe the type of information available on the internet for French-speaking parents of children with disability as well as assess the quality of the information collected. Methods: We carried out a search of the existing relevant websites targeted at parents of children with disability. We used a validated instrument to extract structural, textual, and visual characteristics of these websites and evaluate their usability. Results: In all, 42 websites were analyzed; of these, the information had been validated by a trustworthy source in only 18 (43%) websites. Networking opportunities for parents were available in only 7 (17%) websites. Most websites provided information related to autism spectrum disorder (20/42, 42%) and learning disabilities (19/42, 45%), and only a few websites discussed other disability types such as behavorial disorders and developmental language disorders (4/42, 10% each). Community, social, and civic life (9/42, 22%); domestic life (12/42, 29%); and mobility (15/42, 36%) were the less frequently covered topics. With regard to the usability evaluation, 22 of the 42 (52%) websites received a global score <70%, whereas 20 (48%) scored >= 70% Conclusions: Although the internet is an infinite source of information, it is not necessarily actionable for parents of children with disability. Some information remains difficult to find online, and networking opportunities with other parents dealing with similar challenges are scarce.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] Using Common Determinants of Out-of-Home Care to Profile Parents of Children and Adolescents with a Disability: an Exploratory Study
    Vassos, Maria
    Nankervis, Karen
    Gavidia-Payne, Susana
    Chan, Jeffrey
    ADVANCES IN NEURODEVELOPMENTAL DISORDERS, 2019, 3 (03) : 267 - 280
  • [32] Longitudinal Study of Parents' Impact on Quality of Life of Children and Young Adults with Intellectual Disabilities
    Cramm, Jane M.
    Nieboer, Anna P.
    JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES, 2012, 25 (01) : 20 - 28
  • [33] Quality of life for children with functional abdominal pain: A comparison study of patients' and parents' perceptions
    Youssef, NN
    Murphy, TG
    Langseder, AL
    Rosh, JR
    PEDIATRICS, 2006, 117 (01) : 54 - 59
  • [34] Using Common Determinants of Out-of-Home Care to Profile Parents of Children and Adolescents with a Disability: an Exploratory Study
    Maria Vassos
    Karen Nankervis
    Susana Gavidia-Payne
    Jeffrey Chan
    Advances in Neurodevelopmental Disorders, 2019, 3 : 267 - 280
  • [35] Evaluation of the quality of life of children with celiac disease and their parents: a case-control study
    de Lorenzo, Claudia Maria
    Xikota, Joao Carlos
    Wayhs, Monica Chang
    Nassar, Silvia Modesto
    de Souza Pires, Maria Marlene
    QUALITY OF LIFE RESEARCH, 2012, 21 (01) : 77 - 85
  • [36] Quality of life of children with achondroplasia and their parents-a German cross-sectional study
    Witt, Stefanie
    Kolb, Beate
    Bloemeke, Janika
    Mohnike, Klaus
    Bullinger, Monika
    Quitmann, Julia
    ORPHANET JOURNAL OF RARE DISEASES, 2019, 14 (01)
  • [37] Evaluation of care burden among mothers of children with a disability: Correlation between physical activity, quality of life, and sleep quality; a cross-sectional study
    Yilmaz, Gamze
    Kucuk Alemdar, Dilek
    PERSPECTIVES IN PSYCHIATRIC CARE, 2021, 57 (01) : 129 - 137
  • [38] Caregivers burden in parents of children with hearing impairment and intellectual disability; A cross sectional study from Punjab, Pakistan
    Firdous, Nazia
    Mumtaz, Nazia
    Saqulain, Ghulam
    RAWAL MEDICAL JOURNAL, 2025, 50 (01): : 163 - 166
  • [39] Sleep Quality and Evening Salivary Cortisol Levels in Association with the Psychological Resources of Parents of Children with Developmental Disorders and Type 1 Diabetes
    Ljubicic, Marija
    Sare, Sonja
    Kolcic, Ivana
    JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2025, 55 (04) : 1481 - 1494
  • [40] Content and quality of web-based health information for the prevention and prediction of food allergies in children: A systematic evaluation
    Horold, Madlen
    Rohr, Magdalena
    Beyer, Maja
    Bauer, Theresa
    Konig, Mara
    Gerhardinger, Katharina
    Apfelbacher, Christian
    Brandstetter, Susanne
    ZEITSCHRIFT FUR EVIDENZ FORTBILDUNG UND QUALITAET IM GESUNDHEITSWESEN, 2025, 193 : 45 - 55