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“It's very important that you measure throughout that journey…”: patient perspectives towards quality-of-life data collection following haematopoietic cell transplant

Crossref DOI link: https://doi.org/10.1186/s12885-025-14269-8

Published Online: 2025-05-13

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Pugh, Gemma

Young, Lauren

Yiallouridou, Christina

Hart, Dawn

Dean, Karen

Danby, Robert
Funding

Funding for this research was provided by:

National Institute for Health and Care Research (NIHR205434, NIHR205434, NIHR205434, NIHR205434, NIHR205434)

Therakos UK
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Text and Data Mining valid from 2025-05-13

Version of Record valid from 2025-05-13
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Article History

Received: 8 January 2025

Accepted: 5 May 2025

First Online: 13 May 2025

Declarations

:

: This study was performed in line with the principles of the Declaration of Helsinki.The study underwent a proportionate review and received ethical approval from the Anthony Nolan Research Office.Informed consent was obtained from all individual participants included in the study. Participants consented to interviews being audio-recorded and transcribed and to publication of the findings.

: Not applicable.

: The authors declare no competing interests.

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