Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetes

Abstract Background The literature on the specification and measurement of the outcomes of the healthcare transition from pediatric to adult centered-care is scarce and methodologically weak. To address these gaps, we conducted a series of studies to develop a multidimensional, multi-informant (youn...

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Main Authors: Jessica Pierce, Karen Aroian, Elizabeth Schifano, Anthony Gannon, Tim Wysocki
Format: Article
Language:English
Published: SpringerOpen 2019-12-01
Series:Journal of Patient-Reported Outcomes
Subjects:
Online Access:https://doi.org/10.1186/s41687-019-0163-9
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spelling doaj-457fce355b1849cf98a8e0b4dd7486802020-12-20T12:07:29ZengSpringerOpenJournal of Patient-Reported Outcomes2509-80202019-12-01311810.1186/s41687-019-0163-9Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetesJessica Pierce0Karen Aroian1Elizabeth Schifano2Anthony Gannon3Tim Wysocki4Nemours Children’s HospitalUniversity of Central FloridaNemours Research InstituteNemours/Alfred I duPont Hospital for ChildrenNemours Children’s Specialty CareAbstract Background The literature on the specification and measurement of the outcomes of the healthcare transition from pediatric to adult centered-care is scarce and methodologically weak. To address these gaps, we conducted a series of studies to develop a multidimensional, multi-informant (young adults, parents, and healthcare providers) measure of healthcare transition outcomes for young adults with type 1 diabetes (T1D), the Healthcare Transition Outcomes Inventory (HCTOI). The current study describes the development and refinement of the HCTOI item pool. Methods Following Patient Reported Outcomes Measurement Information System (PROMIS) standards, the research team conducted qualitative interviews to define six content domains of healthcare transition outcomes from the perspectives of multiple stakeholders, developed an initial item pool of the HCTOI based on the six domains, analyzed expert item ratings and feedback for content validation, and conducted cognitive interviews with informants (patients, parents, and healthcare providers) for further item pool refinement. Results Qualitative findings revealed six healthcare transition outcome domains: 1) Biomedical markers of T1D control; 2) Navigation of a new health care system; 3) Possession of T1D self-management skills and knowledge; 4) Integration of T1D care into emerging adult roles; 5) Balance of parental involvement with autonomy; and 6) Attainment of T1D “ownership.” An initial pool of 88 items focused on the extent to which a young adult with T1D is successful on each of the six domains. Experts rated all content domains and all but six items as relevant. In addition to suggesting additional items, experts were concerned about the length of the measure, response burden, and whether every informant type would have sufficient knowledge to rate items in particular content domains. Cognitive interviews resulted in retaining all six content domains, but dropping some items and yielded fewer items for the healthcare provider version (47 items versus 54 items for the young adult- and parent-versions). Conclusions Expert review and cognitive interviews confirmed that all six domains of HCT outcomes were relevant and both procedures resulted in retaining a sufficient number of clear and representative items for each content domain. The HCTOI represents the first multi-informant, rigorously developed item pool that comprehensively measures the multiple components of the transition from pediatric to adult specialty healthcare.https://doi.org/10.1186/s41687-019-0163-9Young adultsMeasure developmentType 1 diabetesHealthcare transition
collection DOAJ
language English
format Article
sources DOAJ
author Jessica Pierce
Karen Aroian
Elizabeth Schifano
Anthony Gannon
Tim Wysocki
spellingShingle Jessica Pierce
Karen Aroian
Elizabeth Schifano
Anthony Gannon
Tim Wysocki
Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetes
Journal of Patient-Reported Outcomes
Young adults
Measure development
Type 1 diabetes
Healthcare transition
author_facet Jessica Pierce
Karen Aroian
Elizabeth Schifano
Anthony Gannon
Tim Wysocki
author_sort Jessica Pierce
title Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetes
title_short Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetes
title_full Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetes
title_fullStr Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetes
title_full_unstemmed Development and content validation of the Healthcare Transition Outcomes Inventory for young adults with type 1 diabetes
title_sort development and content validation of the healthcare transition outcomes inventory for young adults with type 1 diabetes
publisher SpringerOpen
series Journal of Patient-Reported Outcomes
issn 2509-8020
publishDate 2019-12-01
description Abstract Background The literature on the specification and measurement of the outcomes of the healthcare transition from pediatric to adult centered-care is scarce and methodologically weak. To address these gaps, we conducted a series of studies to develop a multidimensional, multi-informant (young adults, parents, and healthcare providers) measure of healthcare transition outcomes for young adults with type 1 diabetes (T1D), the Healthcare Transition Outcomes Inventory (HCTOI). The current study describes the development and refinement of the HCTOI item pool. Methods Following Patient Reported Outcomes Measurement Information System (PROMIS) standards, the research team conducted qualitative interviews to define six content domains of healthcare transition outcomes from the perspectives of multiple stakeholders, developed an initial item pool of the HCTOI based on the six domains, analyzed expert item ratings and feedback for content validation, and conducted cognitive interviews with informants (patients, parents, and healthcare providers) for further item pool refinement. Results Qualitative findings revealed six healthcare transition outcome domains: 1) Biomedical markers of T1D control; 2) Navigation of a new health care system; 3) Possession of T1D self-management skills and knowledge; 4) Integration of T1D care into emerging adult roles; 5) Balance of parental involvement with autonomy; and 6) Attainment of T1D “ownership.” An initial pool of 88 items focused on the extent to which a young adult with T1D is successful on each of the six domains. Experts rated all content domains and all but six items as relevant. In addition to suggesting additional items, experts were concerned about the length of the measure, response burden, and whether every informant type would have sufficient knowledge to rate items in particular content domains. Cognitive interviews resulted in retaining all six content domains, but dropping some items and yielded fewer items for the healthcare provider version (47 items versus 54 items for the young adult- and parent-versions). Conclusions Expert review and cognitive interviews confirmed that all six domains of HCT outcomes were relevant and both procedures resulted in retaining a sufficient number of clear and representative items for each content domain. The HCTOI represents the first multi-informant, rigorously developed item pool that comprehensively measures the multiple components of the transition from pediatric to adult specialty healthcare.
topic Young adults
Measure development
Type 1 diabetes
Healthcare transition
url https://doi.org/10.1186/s41687-019-0163-9
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