Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content Validity

BackgroundThe quality of life of patients at all stages of hematological malignancy is greatly affected by the disease and its treatment. There is a wide range of health-related quality of life (HRQoL) issues important to these patients. Any new instrument developed to measure HRQoL of such patients...

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Main Authors: Pushpendra Goswami, Esther N. Oliva, Tatyana Ionova, Roger Else, Jonathan Kell, Adele K. Fielding, Daniel M. Jennings, Marina Karakantza, Saad Al-Ismail, Graham P. Collins, Stewart McConnell, Catherine Langton, Sam Salek
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-03-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphar.2020.00209/full
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spelling doaj-9c8a24b1f7c948c89f26d7101c026c082020-11-25T02:35:14ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122020-03-011110.3389/fphar.2020.00209473020Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content ValidityPushpendra Goswami0Esther N. Oliva1Tatyana Ionova2Roger Else3Jonathan Kell4Adele K. Fielding5Daniel M. Jennings6Marina Karakantza7Saad Al-Ismail8Graham P. Collins9Stewart McConnell10Catherine Langton11Sam Salek12School of Life and Medical Sciences, University of Hertfordshire, Hatfield, United KingdomHaematology Unit, Grande Ospedale Metropolitano, Reggio Calabria, ItalySt. Petersburg State University Medical Center and Multinational Centre for Quality of Life Research, Saint Petersburg, RussiaPatient Research Partner, Milton Keynes, United KingdomCardiff and Vale University Health Board, Cardiff, United KingdomCancer Institute, University College London, London, United KingdomRoyal Surrey NHS Foundation Trust, Guildford, United KingdomLeeds Teaching Hospitals NHS Trust, Leeds, United KingdomSingleton Hospital, ABM University Health Board, Swansea, United Kingdom0Oxford University Hospital NHS Foundation Trust, Oxford, United KingdomLeeds Teaching Hospitals NHS Trust, Leeds, United KingdomLeeds Teaching Hospitals NHS Trust, Leeds, United KingdomSchool of Life and Medical Sciences, University of Hertfordshire, Hatfield, United KingdomBackgroundThe quality of life of patients at all stages of hematological malignancy is greatly affected by the disease and its treatment. There is a wide range of health-related quality of life (HRQoL) issues important to these patients. Any new instrument developed to measure HRQoL of such patients should be content valid, i.e., the items should be comprehensively relevant to the patients and their health condition. The aim of the present study was to examine content validity of a hematological malignancy specific patient reported outcome measure (HM-PRO) developed for use in routine clinical practice.MethodsFollowing literature review and semi-structured interviews, the generated themes and sub-themes were discussed to develop the prototype version of the HM-PRO. A 4-step approach was used for content validation: initial testing and cognitive interviewing; item rating; content validity panel meeting; final field testing and cognitive interviewing. Additional questions related to patients’ perception of recall period and preferred sentence structure (i.e., question or statement) of the items were also asked during cognitive interviews.ResultsThe content analysis of 129 transcribed semi-structured interviews resulted in the prototype version of the instrument consisting of 58 items grouped into two parts: Part A (impact/HRQoL – 34 items) and Part B (signs and symptoms – 24 items). The initial testing showed intra-class correlation coefficient (ICC) of >0.8 for both Part A and Part B. Item rating for language clarity, completeness, relevance, and response scale by experts and patients showed content validity index for scales average >0.8 for both Part A and Part B, except 0.64 for relevance for Part A by the patient panel. The final testing of the revised version of the instrument showed the Cronbach’s alpha value of 0.91 for Part A and 0.76 for Part B, suggesting high internal consistency, and ICC of 0.91 for Part A and 0.76 for Part B. The recall period of “today” for Part-A and “last 3 days” for Part-B were the patients’ preferred “recall period.” Furthermore, the patients expressed preference to the HM-PRO items as statements.ConclusionThe findings of this study confirm that the HM-PRO possesses a strong content validity, includes all the issues important to patients and is easy to read, understand and respond to spontaneously.https://www.frontiersin.org/article/10.3389/fphar.2020.00209/fullhematological malignancyHM-PROquality of lifesymptomscontent validityclinical practice
collection DOAJ
language English
format Article
sources DOAJ
author Pushpendra Goswami
Esther N. Oliva
Tatyana Ionova
Roger Else
Jonathan Kell
Adele K. Fielding
Daniel M. Jennings
Marina Karakantza
Saad Al-Ismail
Graham P. Collins
Stewart McConnell
Catherine Langton
Sam Salek
spellingShingle Pushpendra Goswami
Esther N. Oliva
Tatyana Ionova
Roger Else
Jonathan Kell
Adele K. Fielding
Daniel M. Jennings
Marina Karakantza
Saad Al-Ismail
Graham P. Collins
Stewart McConnell
Catherine Langton
Sam Salek
Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content Validity
Frontiers in Pharmacology
hematological malignancy
HM-PRO
quality of life
symptoms
content validity
clinical practice
author_facet Pushpendra Goswami
Esther N. Oliva
Tatyana Ionova
Roger Else
Jonathan Kell
Adele K. Fielding
Daniel M. Jennings
Marina Karakantza
Saad Al-Ismail
Graham P. Collins
Stewart McConnell
Catherine Langton
Sam Salek
author_sort Pushpendra Goswami
title Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content Validity
title_short Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content Validity
title_full Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content Validity
title_fullStr Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content Validity
title_full_unstemmed Development of a Novel Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Content Validity
title_sort development of a novel hematological malignancy specific patient-reported outcome measure (hm-pro): content validity
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2020-03-01
description BackgroundThe quality of life of patients at all stages of hematological malignancy is greatly affected by the disease and its treatment. There is a wide range of health-related quality of life (HRQoL) issues important to these patients. Any new instrument developed to measure HRQoL of such patients should be content valid, i.e., the items should be comprehensively relevant to the patients and their health condition. The aim of the present study was to examine content validity of a hematological malignancy specific patient reported outcome measure (HM-PRO) developed for use in routine clinical practice.MethodsFollowing literature review and semi-structured interviews, the generated themes and sub-themes were discussed to develop the prototype version of the HM-PRO. A 4-step approach was used for content validation: initial testing and cognitive interviewing; item rating; content validity panel meeting; final field testing and cognitive interviewing. Additional questions related to patients’ perception of recall period and preferred sentence structure (i.e., question or statement) of the items were also asked during cognitive interviews.ResultsThe content analysis of 129 transcribed semi-structured interviews resulted in the prototype version of the instrument consisting of 58 items grouped into two parts: Part A (impact/HRQoL – 34 items) and Part B (signs and symptoms – 24 items). The initial testing showed intra-class correlation coefficient (ICC) of >0.8 for both Part A and Part B. Item rating for language clarity, completeness, relevance, and response scale by experts and patients showed content validity index for scales average >0.8 for both Part A and Part B, except 0.64 for relevance for Part A by the patient panel. The final testing of the revised version of the instrument showed the Cronbach’s alpha value of 0.91 for Part A and 0.76 for Part B, suggesting high internal consistency, and ICC of 0.91 for Part A and 0.76 for Part B. The recall period of “today” for Part-A and “last 3 days” for Part-B were the patients’ preferred “recall period.” Furthermore, the patients expressed preference to the HM-PRO items as statements.ConclusionThe findings of this study confirm that the HM-PRO possesses a strong content validity, includes all the issues important to patients and is easy to read, understand and respond to spontaneously.
topic hematological malignancy
HM-PRO
quality of life
symptoms
content validity
clinical practice
url https://www.frontiersin.org/article/10.3389/fphar.2020.00209/full
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