Loading…
How to summarise and report written qualitative data from patients: a method for use in cancer support care
The goal of this study is the determination of key themes to aid the analysis of qualitative data collected at three cancer support centres in England, using the Measure Yourself Concerns and Wellbeing (MYCaW) questionnaire. People with cancer who use complementary therapies experience and value a w...
Saved in:
Published in: | Supportive care in cancer 2007-08, Vol.15 (8), p.963-971 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c369t-85da2954ea81d1e74a8ed8750570e4ceb1871b9e8433cbeec11e02d2ba0f5b0e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c369t-85da2954ea81d1e74a8ed8750570e4ceb1871b9e8433cbeec11e02d2ba0f5b0e3 |
container_end_page | 971 |
container_issue | 8 |
container_start_page | 963 |
container_title | Supportive care in cancer |
container_volume | 15 |
creator | Polley, Marie J Seers, Helen E Cooke, Helen J Hoffman, Caroline Paterson, Charlotte |
description | The goal of this study is the determination of key themes to aid the analysis of qualitative data collected at three cancer support centres in England, using the Measure Yourself Concerns and Wellbeing (MYCaW) questionnaire.
People with cancer who use complementary therapies experience and value a wide range of treatment effects, yet tools are urgently required to quantitatively measure these outcomes. MYCaW is an individualised questionnaire used in cancer support centres providing complementary therapies, scoring 'concerns or problems' and 'well-being' and collecting qualitative data about other major events in a patient's life and what has been most important to the patient. Content analysis on 782 MYCaW questionnaires from people at these cancer support centres was carried out. The 'concerns,' 'other things going on in their life' and 'important aspects of centre' were thematically categorised and externally validated by a focus group, and the inter-rater reliability was calculated.
Clinical information from a cancer patient's perspective was collected that is not measured on standard quality-of-life questionnaires; furthermore, some themes acknowledge the multi-faceted aspects of complementary and alternative medicine provision, rather than information only relating to the therapeutic intervention. Categories for qualitative MYCaW analysis have been established providing a tool for future research and/or service delivery improvement within cancer support centres such as these.
The established themes provide a framework to aid analysis of qualitative aspects of complementary therapy care for people with cancer, improving our understanding of how the patient's cancer experience can be aided by complementary therapies in specialised cancer centres. |
doi_str_mv | 10.1007/s00520-007-0283-2 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68171817</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68171817</sourcerecordid><originalsourceid>FETCH-LOGICAL-c369t-85da2954ea81d1e74a8ed8750570e4ceb1871b9e8433cbeec11e02d2ba0f5b0e3</originalsourceid><addsrcrecordid>eNpdkcFq3DAQhkVIabZpHyCXInLIze2MZVlybyEk3cBCL-1ZyPKYOF1bXknukrevNrsQyGGYYfjnY2Z-xq4QviGA-h4BZAlFLgsotSjKM7bCSohCCdGcsxU0FRaVkPKCfYrxGQCVkuVHdoGqxqZBWLG_a7_nyfO4jKMNQyRup44Hmn1IfB-GlGjiu8Vuh2TT8I94Z5PlffAjn3ODphR_cMtHSk--470PfMmMYeLOTo5C5s6vKGcDfWYferuN9OWUL9mfh_vfd-ti8-vn493tpnCiblKhZWfLRlZkNXZIqrKaOq0kSAVUOWpRK2wb0vlS1xI5RIKyK1sLvWyBxCW7OXLn4HcLxWTGITrabu1Efomm1qgwRxZevxM--yVMeTejdYVQ1yCzCI8iF3yMgXozhyH_6sUgmIMN5miDOZQHG0yZZ76ewEs7Uvc2cfq7-A9ONoPG</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>884106605</pqid></control><display><type>article</type><title>How to summarise and report written qualitative data from patients: a method for use in cancer support care</title><source>Springer Nature</source><source>Social Science Premium Collection (Proquest) (PQ_SDU_P3)</source><source>Sociology Collection</source><creator>Polley, Marie J ; Seers, Helen E ; Cooke, Helen J ; Hoffman, Caroline ; Paterson, Charlotte</creator><creatorcontrib>Polley, Marie J ; Seers, Helen E ; Cooke, Helen J ; Hoffman, Caroline ; Paterson, Charlotte</creatorcontrib><description>The goal of this study is the determination of key themes to aid the analysis of qualitative data collected at three cancer support centres in England, using the Measure Yourself Concerns and Wellbeing (MYCaW) questionnaire.
People with cancer who use complementary therapies experience and value a wide range of treatment effects, yet tools are urgently required to quantitatively measure these outcomes. MYCaW is an individualised questionnaire used in cancer support centres providing complementary therapies, scoring 'concerns or problems' and 'well-being' and collecting qualitative data about other major events in a patient's life and what has been most important to the patient. Content analysis on 782 MYCaW questionnaires from people at these cancer support centres was carried out. The 'concerns,' 'other things going on in their life' and 'important aspects of centre' were thematically categorised and externally validated by a focus group, and the inter-rater reliability was calculated.
Clinical information from a cancer patient's perspective was collected that is not measured on standard quality-of-life questionnaires; furthermore, some themes acknowledge the multi-faceted aspects of complementary and alternative medicine provision, rather than information only relating to the therapeutic intervention. Categories for qualitative MYCaW analysis have been established providing a tool for future research and/or service delivery improvement within cancer support centres such as these.
The established themes provide a framework to aid analysis of qualitative aspects of complementary therapy care for people with cancer, improving our understanding of how the patient's cancer experience can be aided by complementary therapies in specialised cancer centres.</description><identifier>ISSN: 0941-4355</identifier><identifier>EISSN: 1433-7339</identifier><identifier>DOI: 10.1007/s00520-007-0283-2</identifier><identifier>PMID: 17619910</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Aged ; Cancer ; Cancer Care Facilities ; Complementary Therapies ; Content analysis ; England ; Evaluation Studies as Topic ; Female ; Humans ; Male ; Middle Aged ; Neoplasms - therapy ; Palliative Care ; Patient Satisfaction ; Studies ; Surveys and Questionnaires</subject><ispartof>Supportive care in cancer, 2007-08, Vol.15 (8), p.963-971</ispartof><rights>Springer-Verlag 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-85da2954ea81d1e74a8ed8750570e4ceb1871b9e8433cbeec11e02d2ba0f5b0e3</citedby><cites>FETCH-LOGICAL-c369t-85da2954ea81d1e74a8ed8750570e4ceb1871b9e8433cbeec11e02d2ba0f5b0e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/884106605/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/884106605?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,21394,21395,27924,27925,33611,33612,34530,34531,43733,44115,74221,74639</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17619910$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Polley, Marie J</creatorcontrib><creatorcontrib>Seers, Helen E</creatorcontrib><creatorcontrib>Cooke, Helen J</creatorcontrib><creatorcontrib>Hoffman, Caroline</creatorcontrib><creatorcontrib>Paterson, Charlotte</creatorcontrib><title>How to summarise and report written qualitative data from patients: a method for use in cancer support care</title><title>Supportive care in cancer</title><addtitle>Support Care Cancer</addtitle><description>The goal of this study is the determination of key themes to aid the analysis of qualitative data collected at three cancer support centres in England, using the Measure Yourself Concerns and Wellbeing (MYCaW) questionnaire.
People with cancer who use complementary therapies experience and value a wide range of treatment effects, yet tools are urgently required to quantitatively measure these outcomes. MYCaW is an individualised questionnaire used in cancer support centres providing complementary therapies, scoring 'concerns or problems' and 'well-being' and collecting qualitative data about other major events in a patient's life and what has been most important to the patient. Content analysis on 782 MYCaW questionnaires from people at these cancer support centres was carried out. The 'concerns,' 'other things going on in their life' and 'important aspects of centre' were thematically categorised and externally validated by a focus group, and the inter-rater reliability was calculated.
Clinical information from a cancer patient's perspective was collected that is not measured on standard quality-of-life questionnaires; furthermore, some themes acknowledge the multi-faceted aspects of complementary and alternative medicine provision, rather than information only relating to the therapeutic intervention. Categories for qualitative MYCaW analysis have been established providing a tool for future research and/or service delivery improvement within cancer support centres such as these.
The established themes provide a framework to aid analysis of qualitative aspects of complementary therapy care for people with cancer, improving our understanding of how the patient's cancer experience can be aided by complementary therapies in specialised cancer centres.</description><subject>Aged</subject><subject>Cancer</subject><subject>Cancer Care Facilities</subject><subject>Complementary Therapies</subject><subject>Content analysis</subject><subject>England</subject><subject>Evaluation Studies as Topic</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasms - therapy</subject><subject>Palliative Care</subject><subject>Patient Satisfaction</subject><subject>Studies</subject><subject>Surveys and Questionnaires</subject><issn>0941-4355</issn><issn>1433-7339</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>ALSLI</sourceid><sourceid>HEHIP</sourceid><sourceid>M2R</sourceid><sourceid>M2S</sourceid><recordid>eNpdkcFq3DAQhkVIabZpHyCXInLIze2MZVlybyEk3cBCL-1ZyPKYOF1bXknukrevNrsQyGGYYfjnY2Z-xq4QviGA-h4BZAlFLgsotSjKM7bCSohCCdGcsxU0FRaVkPKCfYrxGQCVkuVHdoGqxqZBWLG_a7_nyfO4jKMNQyRup44Hmn1IfB-GlGjiu8Vuh2TT8I94Z5PlffAjn3ODphR_cMtHSk--470PfMmMYeLOTo5C5s6vKGcDfWYferuN9OWUL9mfh_vfd-ti8-vn493tpnCiblKhZWfLRlZkNXZIqrKaOq0kSAVUOWpRK2wb0vlS1xI5RIKyK1sLvWyBxCW7OXLn4HcLxWTGITrabu1Efomm1qgwRxZevxM--yVMeTejdYVQ1yCzCI8iF3yMgXozhyH_6sUgmIMN5miDOZQHG0yZZ76ewEs7Uvc2cfq7-A9ONoPG</recordid><startdate>20070801</startdate><enddate>20070801</enddate><creator>Polley, Marie J</creator><creator>Seers, Helen E</creator><creator>Cooke, Helen J</creator><creator>Hoffman, Caroline</creator><creator>Paterson, Charlotte</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88J</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HEHIP</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2R</scope><scope>M2S</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20070801</creationdate><title>How to summarise and report written qualitative data from patients: a method for use in cancer support care</title><author>Polley, Marie J ; Seers, Helen E ; Cooke, Helen J ; Hoffman, Caroline ; Paterson, Charlotte</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-85da2954ea81d1e74a8ed8750570e4ceb1871b9e8433cbeec11e02d2ba0f5b0e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Aged</topic><topic>Cancer</topic><topic>Cancer Care Facilities</topic><topic>Complementary Therapies</topic><topic>Content analysis</topic><topic>England</topic><topic>Evaluation Studies as Topic</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasms - therapy</topic><topic>Palliative Care</topic><topic>Patient Satisfaction</topic><topic>Studies</topic><topic>Surveys and Questionnaires</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Polley, Marie J</creatorcontrib><creatorcontrib>Seers, Helen E</creatorcontrib><creatorcontrib>Cooke, Helen J</creatorcontrib><creatorcontrib>Hoffman, Caroline</creatorcontrib><creatorcontrib>Paterson, Charlotte</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Social Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Social Science Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Sociology Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Social Science Database (ProQuest)</collection><collection>Sociology Database (ProQuest)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Supportive care in cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Polley, Marie J</au><au>Seers, Helen E</au><au>Cooke, Helen J</au><au>Hoffman, Caroline</au><au>Paterson, Charlotte</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>How to summarise and report written qualitative data from patients: a method for use in cancer support care</atitle><jtitle>Supportive care in cancer</jtitle><addtitle>Support Care Cancer</addtitle><date>2007-08-01</date><risdate>2007</risdate><volume>15</volume><issue>8</issue><spage>963</spage><epage>971</epage><pages>963-971</pages><issn>0941-4355</issn><eissn>1433-7339</eissn><abstract>The goal of this study is the determination of key themes to aid the analysis of qualitative data collected at three cancer support centres in England, using the Measure Yourself Concerns and Wellbeing (MYCaW) questionnaire.
People with cancer who use complementary therapies experience and value a wide range of treatment effects, yet tools are urgently required to quantitatively measure these outcomes. MYCaW is an individualised questionnaire used in cancer support centres providing complementary therapies, scoring 'concerns or problems' and 'well-being' and collecting qualitative data about other major events in a patient's life and what has been most important to the patient. Content analysis on 782 MYCaW questionnaires from people at these cancer support centres was carried out. The 'concerns,' 'other things going on in their life' and 'important aspects of centre' were thematically categorised and externally validated by a focus group, and the inter-rater reliability was calculated.
Clinical information from a cancer patient's perspective was collected that is not measured on standard quality-of-life questionnaires; furthermore, some themes acknowledge the multi-faceted aspects of complementary and alternative medicine provision, rather than information only relating to the therapeutic intervention. Categories for qualitative MYCaW analysis have been established providing a tool for future research and/or service delivery improvement within cancer support centres such as these.
The established themes provide a framework to aid analysis of qualitative aspects of complementary therapy care for people with cancer, improving our understanding of how the patient's cancer experience can be aided by complementary therapies in specialised cancer centres.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>17619910</pmid><doi>10.1007/s00520-007-0283-2</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0941-4355 |
ispartof | Supportive care in cancer, 2007-08, Vol.15 (8), p.963-971 |
issn | 0941-4355 1433-7339 |
language | eng |
recordid | cdi_proquest_miscellaneous_68171817 |
source | Springer Nature; Social Science Premium Collection (Proquest) (PQ_SDU_P3); Sociology Collection |
subjects | Aged Cancer Cancer Care Facilities Complementary Therapies Content analysis England Evaluation Studies as Topic Female Humans Male Middle Aged Neoplasms - therapy Palliative Care Patient Satisfaction Studies Surveys and Questionnaires |
title | How to summarise and report written qualitative data from patients: a method for use in cancer support care |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T19%3A38%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=How%20to%20summarise%20and%20report%20written%20qualitative%20data%20from%20patients:%20a%20method%20for%20use%20in%20cancer%20support%20care&rft.jtitle=Supportive%20care%20in%20cancer&rft.au=Polley,%20Marie%20J&rft.date=2007-08-01&rft.volume=15&rft.issue=8&rft.spage=963&rft.epage=971&rft.pages=963-971&rft.issn=0941-4355&rft.eissn=1433-7339&rft_id=info:doi/10.1007/s00520-007-0283-2&rft_dat=%3Cproquest_cross%3E68171817%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c369t-85da2954ea81d1e74a8ed8750570e4ceb1871b9e8433cbeec11e02d2ba0f5b0e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=884106605&rft_id=info:pmid/17619910&rfr_iscdi=true |