Exciting but exhausting: experiences with participatory research with chronically ill adolescents
Background Adolescents with chronic conditions are major users of paediatric hospitals, but seldom participate in the evaluation of services or in research. Little is known about the usefulness of the participatory approach in adolescent health research. Objective To evaluate the feasibility, bene...
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description | Background Adolescents with chronic conditions are major users of paediatric hospitals, but seldom participate in the evaluation of services or in research. Little is known about the usefulness of the participatory approach in adolescent health research.
Objective To evaluate the feasibility, benefits and limitations of a participatory research (PR) project involving chronically ill adolescents as co‐researchers.
Design, setting and participants Nine adolescents, aged 15–17 years, acted as co‐researchers in a hospital‐based PR project. They co‐developed an interview protocol and during a disco party held for this purpose interviewed each other and 25 fellow patients (12–19 years). They provided advice on the draft report and participated in the dissemination of the results, but were not involved in the design of the project or analysis of results.
Results Involving adolescents in participatory health research was feasible and appreciated by researchers and youth alike, but had its drawbacks too. The peer‐research attracted few participants, the interviews lacked depth and did not yield substantial new insights. Maintaining a high level of participation of the chronically ill co‐researchers also proved difficult.
Conclusions Adolescents with chronic conditions like to have a say in the design and evaluation of hospital services. But their participation as co‐researchers demands ample resources from all parties involved without automatically improving research quality. PR does not seem the most effective and efficient way to make services more responsive. We therefore recommend further exploration of other creative and sustainable ways for involving youth in health‐care service development and innovation. |
doi_str_mv | 10.1111/j.1369-7625.2009.00574.x |
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Objective To evaluate the feasibility, benefits and limitations of a participatory research (PR) project involving chronically ill adolescents as co‐researchers.
Design, setting and participants Nine adolescents, aged 15–17 years, acted as co‐researchers in a hospital‐based PR project. They co‐developed an interview protocol and during a disco party held for this purpose interviewed each other and 25 fellow patients (12–19 years). They provided advice on the draft report and participated in the dissemination of the results, but were not involved in the design of the project or analysis of results.
Results Involving adolescents in participatory health research was feasible and appreciated by researchers and youth alike, but had its drawbacks too. The peer‐research attracted few participants, the interviews lacked depth and did not yield substantial new insights. Maintaining a high level of participation of the chronically ill co‐researchers also proved difficult.
Conclusions Adolescents with chronic conditions like to have a say in the design and evaluation of hospital services. But their participation as co‐researchers demands ample resources from all parties involved without automatically improving research quality. PR does not seem the most effective and efficient way to make services more responsive. We therefore recommend further exploration of other creative and sustainable ways for involving youth in health‐care service development and innovation.</description><identifier>ISSN: 1369-6513</identifier><identifier>EISSN: 1369-7625</identifier><identifier>DOI: 10.1111/j.1369-7625.2009.00574.x</identifier><identifier>PMID: 19682098</identifier><identifier>CODEN: HEHPFM</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; adolescent health services ; Adolescents ; Archives & records ; Child care ; Children & youth ; Chronic conditions ; Chronic Disease ; Chronic illnesses ; Chronic sickness ; Clinical nursing ; collaborative ; Consumer Involvement in Research ; Decision making ; Design ; Diabetes ; Dissemination ; evaluation ; Feasibility ; Feasibility Studies ; Female ; Health care ; Health education ; Health promotion ; Health services ; Health Services Research ; Health status ; Hospitals ; Hospitals, Pediatric ; Humans ; Innovations ; Interviews ; Interviews as Topic ; Male ; Medical research ; Netherlands ; Participation ; Participatory research ; Patient education ; Patient Participation ; Pediatrics ; Public health ; Qualitative research ; Quality of Health Care ; Sick adolescents ; Society ; Teenagers ; Usefulness ; Young Adult</subject><ispartof>Health expectations : an international journal of public participation in health care and health policy, 2010-03, Vol.13 (1), p.95-107</ispartof><rights>2009 The Authors. Journal compilation © 2009 Blackwell Publishing Ltd</rights><rights>2010. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6014-642467e7a2719c97d88d71e3c8ea1b9418a533c3b850afe22918c0dfac236f243</citedby><cites>FETCH-LOGICAL-c6014-642467e7a2719c97d88d71e3c8ea1b9418a533c3b850afe22918c0dfac236f243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5060512/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5060512/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,11562,27924,27925,30999,31000,53791,53793</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1369-7625.2009.00574.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19682098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Van Staa, AnneLoes</creatorcontrib><creatorcontrib>Jedeloo, Susan</creatorcontrib><creatorcontrib>Latour, Jos M</creatorcontrib><creatorcontrib>Trappenburg, Margo J</creatorcontrib><title>Exciting but exhausting: experiences with participatory research with chronically ill adolescents</title><title>Health expectations : an international journal of public participation in health care and health policy</title><addtitle>Health Expect</addtitle><description>Background Adolescents with chronic conditions are major users of paediatric hospitals, but seldom participate in the evaluation of services or in research. Little is known about the usefulness of the participatory approach in adolescent health research.
Objective To evaluate the feasibility, benefits and limitations of a participatory research (PR) project involving chronically ill adolescents as co‐researchers.
Design, setting and participants Nine adolescents, aged 15–17 years, acted as co‐researchers in a hospital‐based PR project. They co‐developed an interview protocol and during a disco party held for this purpose interviewed each other and 25 fellow patients (12–19 years). They provided advice on the draft report and participated in the dissemination of the results, but were not involved in the design of the project or analysis of results.
Results Involving adolescents in participatory health research was feasible and appreciated by researchers and youth alike, but had its drawbacks too. The peer‐research attracted few participants, the interviews lacked depth and did not yield substantial new insights. Maintaining a high level of participation of the chronically ill co‐researchers also proved difficult.
Conclusions Adolescents with chronic conditions like to have a say in the design and evaluation of hospital services. But their participation as co‐researchers demands ample resources from all parties involved without automatically improving research quality. PR does not seem the most effective and efficient way to make services more responsive. We therefore recommend further exploration of other creative and sustainable ways for involving youth in health‐care service development and innovation.</description><subject>Adolescent</subject><subject>adolescent health services</subject><subject>Adolescents</subject><subject>Archives & records</subject><subject>Child care</subject><subject>Children & youth</subject><subject>Chronic conditions</subject><subject>Chronic Disease</subject><subject>Chronic illnesses</subject><subject>Chronic sickness</subject><subject>Clinical nursing</subject><subject>collaborative</subject><subject>Consumer Involvement in Research</subject><subject>Decision making</subject><subject>Design</subject><subject>Diabetes</subject><subject>Dissemination</subject><subject>evaluation</subject><subject>Feasibility</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Health care</subject><subject>Health education</subject><subject>Health promotion</subject><subject>Health services</subject><subject>Health Services Research</subject><subject>Health status</subject><subject>Hospitals</subject><subject>Hospitals, Pediatric</subject><subject>Humans</subject><subject>Innovations</subject><subject>Interviews</subject><subject>Interviews as Topic</subject><subject>Male</subject><subject>Medical research</subject><subject>Netherlands</subject><subject>Participation</subject><subject>Participatory research</subject><subject>Patient education</subject><subject>Patient Participation</subject><subject>Pediatrics</subject><subject>Public health</subject><subject>Qualitative research</subject><subject>Quality of Health Care</subject><subject>Sick adolescents</subject><subject>Society</subject><subject>Teenagers</subject><subject>Usefulness</subject><subject>Young Adult</subject><issn>1369-6513</issn><issn>1369-7625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqNkttu1DAQhiMEoqXwCigSElwl-JD4gBASKttt1QouOJS7kddxul68SbATmn17HLJaDheAbzzWfP9YM_MnSYpRjuN5vskxZTLjjJQ5QUjmCJW8yMc7yfEhcXcfsxLTo-RBCBuEMKeC30-OsGSCICmOE7UYte1tc5Ouhj4141oNYXq-iHFnvDWNNiG9tf067ZTvrbad6lu_S70JRnm9nnN67dvGauXcLrXOpapqnQnaNH14mNyrlQvm0f4-ST6eLT6cnmdX75YXp6-vMs0QLjJWkIJxwxXhWGrJKyEqjg3Vwii8kgUWqqRU05UokaoNIRILjapaaUJZTQp6krya63bDamuq6W-vHHTebpXfQass_J5p7Bpu2m9QIoZKTGKBZ_sCvv06mNDD1sYWnFONaYcAAos4PsTZP0lOqSwJIiiST_9KlpxGsJjAJ3-Am3bwTRwYUMTiPiWRPFJiprRvQ_CmPrSHEUzOgA1MS4fJADA5A344A8YoffzreH4K91aIwMsZuLXO7P67MJwvPscgyrNZbkNvxoNc-S_AOOUlXL9dwtnl9Zvlp0LCe_odCRLX0A</recordid><startdate>201003</startdate><enddate>201003</enddate><creator>Van Staa, AnneLoes</creator><creator>Jedeloo, Susan</creator><creator>Latour, Jos M</creator><creator>Trappenburg, Margo J</creator><general>Blackwell Publishing Ltd</general><general>John Wiley & Sons, Inc</general><scope>BSCLL</scope><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>7QJ</scope><scope>7T2</scope><scope>ASE</scope><scope>C1K</scope><scope>FPQ</scope><scope>K6X</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201003</creationdate><title>Exciting but exhausting: experiences with participatory research with chronically ill adolescents</title><author>Van Staa, AnneLoes ; Jedeloo, Susan ; Latour, Jos M ; Trappenburg, Margo J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6014-642467e7a2719c97d88d71e3c8ea1b9418a533c3b850afe22918c0dfac236f243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>adolescent health services</topic><topic>Adolescents</topic><topic>Archives & records</topic><topic>Child care</topic><topic>Children & youth</topic><topic>Chronic conditions</topic><topic>Chronic Disease</topic><topic>Chronic illnesses</topic><topic>Chronic sickness</topic><topic>Clinical nursing</topic><topic>collaborative</topic><topic>Consumer Involvement in Research</topic><topic>Decision making</topic><topic>Design</topic><topic>Diabetes</topic><topic>Dissemination</topic><topic>evaluation</topic><topic>Feasibility</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>Health care</topic><topic>Health education</topic><topic>Health promotion</topic><topic>Health services</topic><topic>Health Services Research</topic><topic>Health status</topic><topic>Hospitals</topic><topic>Hospitals, Pediatric</topic><topic>Humans</topic><topic>Innovations</topic><topic>Interviews</topic><topic>Interviews as Topic</topic><topic>Male</topic><topic>Medical research</topic><topic>Netherlands</topic><topic>Participation</topic><topic>Participatory research</topic><topic>Patient education</topic><topic>Patient Participation</topic><topic>Pediatrics</topic><topic>Public health</topic><topic>Qualitative research</topic><topic>Quality of Health Care</topic><topic>Sick adolescents</topic><topic>Society</topic><topic>Teenagers</topic><topic>Usefulness</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Van Staa, AnneLoes</creatorcontrib><creatorcontrib>Jedeloo, Susan</creatorcontrib><creatorcontrib>Latour, Jos M</creatorcontrib><creatorcontrib>Trappenburg, Margo J</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>British Nursing Index</collection><collection>Environmental Sciences and Pollution Management</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Health expectations : an international journal of public participation in health care and health policy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Van Staa, AnneLoes</au><au>Jedeloo, Susan</au><au>Latour, Jos M</au><au>Trappenburg, Margo J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exciting but exhausting: experiences with participatory research with chronically ill adolescents</atitle><jtitle>Health expectations : an international journal of public participation in health care and health policy</jtitle><addtitle>Health Expect</addtitle><date>2010-03</date><risdate>2010</risdate><volume>13</volume><issue>1</issue><spage>95</spage><epage>107</epage><pages>95-107</pages><issn>1369-6513</issn><eissn>1369-7625</eissn><coden>HEHPFM</coden><abstract>Background Adolescents with chronic conditions are major users of paediatric hospitals, but seldom participate in the evaluation of services or in research. Little is known about the usefulness of the participatory approach in adolescent health research.
Objective To evaluate the feasibility, benefits and limitations of a participatory research (PR) project involving chronically ill adolescents as co‐researchers.
Design, setting and participants Nine adolescents, aged 15–17 years, acted as co‐researchers in a hospital‐based PR project. They co‐developed an interview protocol and during a disco party held for this purpose interviewed each other and 25 fellow patients (12–19 years). They provided advice on the draft report and participated in the dissemination of the results, but were not involved in the design of the project or analysis of results.
Results Involving adolescents in participatory health research was feasible and appreciated by researchers and youth alike, but had its drawbacks too. The peer‐research attracted few participants, the interviews lacked depth and did not yield substantial new insights. Maintaining a high level of participation of the chronically ill co‐researchers also proved difficult.
Conclusions Adolescents with chronic conditions like to have a say in the design and evaluation of hospital services. But their participation as co‐researchers demands ample resources from all parties involved without automatically improving research quality. PR does not seem the most effective and efficient way to make services more responsive. We therefore recommend further exploration of other creative and sustainable ways for involving youth in health‐care service development and innovation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19682098</pmid><doi>10.1111/j.1369-7625.2009.00574.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent adolescent health services Adolescents Archives & records Child care Children & youth Chronic conditions Chronic Disease Chronic illnesses Chronic sickness Clinical nursing collaborative Consumer Involvement in Research Decision making Design Diabetes Dissemination evaluation Feasibility Feasibility Studies Female Health care Health education Health promotion Health services Health Services Research Health status Hospitals Hospitals, Pediatric Humans Innovations Interviews Interviews as Topic Male Medical research Netherlands Participation Participatory research Patient education Patient Participation Pediatrics Public health Qualitative research Quality of Health Care Sick adolescents Society Teenagers Usefulness Young Adult |
title | Exciting but exhausting: experiences with participatory research with chronically ill adolescents |
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