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Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness
BACKGROUND: Families play a critical role in supporting the health and well-being of children with chronic illnesses, who face a lifetime of responsibility for self-management of their condition. Our goal was to investigate whether the novel Patient-Reported Outcomes Measurement Information System®...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194608/ https://www.ncbi.nlm.nih.gov/pubmed/30340500 http://dx.doi.org/10.1186/s12955-018-1030-8 |
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author | Flynn, Kathryn E. Kliems, Harald Saoji, Nikita Svenson, Jacob Cox, Elizabeth D. |
author_facet | Flynn, Kathryn E. Kliems, Harald Saoji, Nikita Svenson, Jacob Cox, Elizabeth D. |
author_sort | Flynn, Kathryn E. |
collection | PubMed |
description | BACKGROUND: Families play a critical role in supporting the health and well-being of children with chronic illnesses, who face a lifetime of responsibility for self-management of their condition. Our goal was to investigate whether the novel Patient-Reported Outcomes Measurement Information System® (PROMIS®) Pediatric Family Relationships measure, developed primarily within the general pediatric population, reflects the experiences of family relationships for chronically ill children and their parents. METHODS: We conducted semi-structured qualitative interviews with children (aged 8–17) with common chronic conditions: asthma (n = 6), type 1 diabetes (n = 5), or sickle cell disease (n = 5), and separately with one of their parents (n = 16). Interviews were recorded, and two team members independently coded the written transcripts facilitated by Nvivo 10. The systematic content analysis used a combination of: 1) pre-specified themes corresponding to the six facets of the domain identified during measure development and reflected in the content of the items (i.e., Sense of Family; Love and Caring; Value and Acceptance; Trust, Dependability, and Support; Communication; Enjoyment), as well as 2) open-coding, allowing participants to define important concepts (i.e., disease impact). RESULTS: Family relationships were conceptualized in a similar way to the general population, as evidenced by child and parent responses to open-ended questions about family relationships and to specific probes that corresponded with the item content in the Family Relationship 8-item short form. Children spontaneously discussed the impact of their disease on family relationships less often than parents did. Although participants described how living with a chronic illness positively and negatively impacted aspects of family relationships, nearly all participants believed their responses to the PROMIS® Family Relationships items would not change if they (or their child) did not have a chronic illness. CONCLUSIONS: Among a sample of families of children with one of 3 chronic illnesses, participants described family relationships in a way that was consistent with the facets of the PROMIS® Family Relationship domain. This study adds to the content validity of the measure for children with chronic illness. |
format | Online Article Text |
id | pubmed-6194608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61946082018-10-25 Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness Flynn, Kathryn E. Kliems, Harald Saoji, Nikita Svenson, Jacob Cox, Elizabeth D. Health Qual Life Outcomes Research BACKGROUND: Families play a critical role in supporting the health and well-being of children with chronic illnesses, who face a lifetime of responsibility for self-management of their condition. Our goal was to investigate whether the novel Patient-Reported Outcomes Measurement Information System® (PROMIS®) Pediatric Family Relationships measure, developed primarily within the general pediatric population, reflects the experiences of family relationships for chronically ill children and their parents. METHODS: We conducted semi-structured qualitative interviews with children (aged 8–17) with common chronic conditions: asthma (n = 6), type 1 diabetes (n = 5), or sickle cell disease (n = 5), and separately with one of their parents (n = 16). Interviews were recorded, and two team members independently coded the written transcripts facilitated by Nvivo 10. The systematic content analysis used a combination of: 1) pre-specified themes corresponding to the six facets of the domain identified during measure development and reflected in the content of the items (i.e., Sense of Family; Love and Caring; Value and Acceptance; Trust, Dependability, and Support; Communication; Enjoyment), as well as 2) open-coding, allowing participants to define important concepts (i.e., disease impact). RESULTS: Family relationships were conceptualized in a similar way to the general population, as evidenced by child and parent responses to open-ended questions about family relationships and to specific probes that corresponded with the item content in the Family Relationship 8-item short form. Children spontaneously discussed the impact of their disease on family relationships less often than parents did. Although participants described how living with a chronic illness positively and negatively impacted aspects of family relationships, nearly all participants believed their responses to the PROMIS® Family Relationships items would not change if they (or their child) did not have a chronic illness. CONCLUSIONS: Among a sample of families of children with one of 3 chronic illnesses, participants described family relationships in a way that was consistent with the facets of the PROMIS® Family Relationship domain. This study adds to the content validity of the measure for children with chronic illness. BioMed Central 2018-10-19 /pmc/articles/PMC6194608/ /pubmed/30340500 http://dx.doi.org/10.1186/s12955-018-1030-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Flynn, Kathryn E. Kliems, Harald Saoji, Nikita Svenson, Jacob Cox, Elizabeth D. Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness |
title | Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness |
title_full | Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness |
title_fullStr | Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness |
title_full_unstemmed | Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness |
title_short | Content validity of the PROMIS® pediatric family relationships measure for children with chronic illness |
title_sort | content validity of the promis® pediatric family relationships measure for children with chronic illness |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194608/ https://www.ncbi.nlm.nih.gov/pubmed/30340500 http://dx.doi.org/10.1186/s12955-018-1030-8 |
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