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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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 |
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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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