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Content validation of a self-report daily diary in patients with sickle cell disease

BACKGROUND: Sickle Cell Disease (SCD) is a genetic progressive vascular disease that impacts patients overall health and quality of life. Sickle-cell pain crises (SCPCs) are a hallmark clinical presentation of SCD and have been associated with increased morbidity and mortality. The Sickle Cell Pain...

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Autores principales: White, Michelle K., Saucier, Cory, Bailey, Miranda, D’Alessio, Denise, Foster, April, St. Pierre, Danielle, Raymond, Kimberly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316505/
https://www.ncbi.nlm.nih.gov/pubmed/34318378
http://dx.doi.org/10.1186/s41687-021-00337-7
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author White, Michelle K.
Saucier, Cory
Bailey, Miranda
D’Alessio, Denise
Foster, April
St. Pierre, Danielle
Raymond, Kimberly
author_facet White, Michelle K.
Saucier, Cory
Bailey, Miranda
D’Alessio, Denise
Foster, April
St. Pierre, Danielle
Raymond, Kimberly
author_sort White, Michelle K.
collection PubMed
description BACKGROUND: Sickle Cell Disease (SCD) is a genetic progressive vascular disease that impacts patients overall health and quality of life. Sickle-cell pain crises (SCPCs) are a hallmark clinical presentation of SCD and have been associated with increased morbidity and mortality. The Sickle Cell Pain Diary- Self Report (SCPD-S) was developed as a daily patient-reported outcome (PRO) measure primarily intended to capture the frequency and severity of SCD-related pain during and outside of a SCPC. The SCPD-S also examines the impact of the pain associated with an SCPC on other health-related quality of life concepts. The objective of this study was to investigate the content validity of the SCPD-S. METHODS: The content validation testing included 18 in-depth hybrid concept elicitation and cognitive debriefing interviews conducted with SCD patients in the US aged 12 years and older. Interviewers used a semi-structured interview guide and a think-aloud approach for the cognitive debriefing portion. All interviews were recorded, transcribed, coded and analyzed. RESULTS: Eighteen interviews across two rounds were conducted. Round 1 hybrid interviews (n = 12) resulted in the expansion of the SCPD-S from 13 to 19 items. Items on the impact of an SCPC on social and recreational activities, sleep, and emotional well-being were added. Five items were significantly revised, as were three response choice sets. Round 2 hybrid interviews (n = 6) confirmed the comprehensiveness of the revised diary, understandability of the wording, and appropriateness of the recall period and response sets. Saturation analyses specific to concept elicitation revealed that no additional interviews were needed. CONCLUSIONS: This study provided evidence to support the content validity of the SCPD-S, a self-report daily diary. Data gathered during patient interviews indicated that the SCPD-S is a fit for purpose measure of SCD and SCPC-related pain frequency and severity and the impact of this pain on other health-related quality of life concepts including fatigue and emotional health. The numerous changes to the SCPD-S as a result of the study findings highlight the importance of the content validation process when developing a PRO measure.
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spelling pubmed-83165052021-08-02 Content validation of a self-report daily diary in patients with sickle cell disease White, Michelle K. Saucier, Cory Bailey, Miranda D’Alessio, Denise Foster, April St. Pierre, Danielle Raymond, Kimberly J Patient Rep Outcomes Research BACKGROUND: Sickle Cell Disease (SCD) is a genetic progressive vascular disease that impacts patients overall health and quality of life. Sickle-cell pain crises (SCPCs) are a hallmark clinical presentation of SCD and have been associated with increased morbidity and mortality. The Sickle Cell Pain Diary- Self Report (SCPD-S) was developed as a daily patient-reported outcome (PRO) measure primarily intended to capture the frequency and severity of SCD-related pain during and outside of a SCPC. The SCPD-S also examines the impact of the pain associated with an SCPC on other health-related quality of life concepts. The objective of this study was to investigate the content validity of the SCPD-S. METHODS: The content validation testing included 18 in-depth hybrid concept elicitation and cognitive debriefing interviews conducted with SCD patients in the US aged 12 years and older. Interviewers used a semi-structured interview guide and a think-aloud approach for the cognitive debriefing portion. All interviews were recorded, transcribed, coded and analyzed. RESULTS: Eighteen interviews across two rounds were conducted. Round 1 hybrid interviews (n = 12) resulted in the expansion of the SCPD-S from 13 to 19 items. Items on the impact of an SCPC on social and recreational activities, sleep, and emotional well-being were added. Five items were significantly revised, as were three response choice sets. Round 2 hybrid interviews (n = 6) confirmed the comprehensiveness of the revised diary, understandability of the wording, and appropriateness of the recall period and response sets. Saturation analyses specific to concept elicitation revealed that no additional interviews were needed. CONCLUSIONS: This study provided evidence to support the content validity of the SCPD-S, a self-report daily diary. Data gathered during patient interviews indicated that the SCPD-S is a fit for purpose measure of SCD and SCPC-related pain frequency and severity and the impact of this pain on other health-related quality of life concepts including fatigue and emotional health. The numerous changes to the SCPD-S as a result of the study findings highlight the importance of the content validation process when developing a PRO measure. Springer International Publishing 2021-07-27 /pmc/articles/PMC8316505/ /pubmed/34318378 http://dx.doi.org/10.1186/s41687-021-00337-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
White, Michelle K.
Saucier, Cory
Bailey, Miranda
D’Alessio, Denise
Foster, April
St. Pierre, Danielle
Raymond, Kimberly
Content validation of a self-report daily diary in patients with sickle cell disease
title Content validation of a self-report daily diary in patients with sickle cell disease
title_full Content validation of a self-report daily diary in patients with sickle cell disease
title_fullStr Content validation of a self-report daily diary in patients with sickle cell disease
title_full_unstemmed Content validation of a self-report daily diary in patients with sickle cell disease
title_short Content validation of a self-report daily diary in patients with sickle cell disease
title_sort content validation of a self-report daily diary in patients with sickle cell disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316505/
https://www.ncbi.nlm.nih.gov/pubmed/34318378
http://dx.doi.org/10.1186/s41687-021-00337-7
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