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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®...

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Autores principales: Flynn, Kathryn E., Kliems, Harald, Saoji, Nikita, Svenson, Jacob, Cox, Elizabeth D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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.
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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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