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Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community
The Genetic, Undiagnosed and Rare Disease community faces a range of hurdles to live their ‘best life’ including physical, social and psychological barriers. They are also resilient and experiential experts with insight into what works and what could work for them. In this study, we aimed to identif...
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Published in: | Journal of community genetics 2023-06, Vol.14 (3), p.295-305 |
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creator | Beadell, Inez Byun, Malia Feller, Hollie Ferrie, Monica Best, Stephanie |
description | The Genetic, Undiagnosed and Rare Disease community faces a range of hurdles to live their ‘best life’ including physical, social and psychological barriers. They are also resilient and experiential experts with insight into what works and what could work for them. In this study, we aimed to identify and prioritise practical interventions the Genetic, Undiagnosed and Rare Disease community report could help them to ‘live well’. Using a three-stage approach, we first analysed data from a year-long Genetic, Undiagnosed and Rare Disease journal study to record all the practical interventions reported, either trialled or proposed. Second, after grouping the interventions (
n
= 19) into four themes (support for individuals with GUaRD; support for carers of people with GUaRD; education/employment; transition), we presented the interventions to members of the GUaRD community (people with GUaRD, their carers and peer support group members) across three focus groups (
n
= 13). Focus group transcripts were analysed for refinements to the interventions, barriers and/or enablers to enacting them and for any additional interventions suggested. From this analysis, the interventions were grouped to identify specific actionable activities (
n
= 8). Finally, these eight interventions were discussed in a workshop with the GUaRD Community Advisory Group and prioritised using the APEASE framework. Prioritised interventions targeted a range of stakeholders and included creating a lived experience video library, supporting peer support groups with grant applications, and educating clinicians about referring to peer support groups. Further research is now required to test these findings before trialling and evaluating an intervention to measure the impact on the GUaRD community. |
doi_str_mv | 10.1007/s12687-023-00643-1 |
format | article |
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n
= 19) into four themes (support for individuals with GUaRD; support for carers of people with GUaRD; education/employment; transition), we presented the interventions to members of the GUaRD community (people with GUaRD, their carers and peer support group members) across three focus groups (
n
= 13). Focus group transcripts were analysed for refinements to the interventions, barriers and/or enablers to enacting them and for any additional interventions suggested. From this analysis, the interventions were grouped to identify specific actionable activities (
n
= 8). Finally, these eight interventions were discussed in a workshop with the GUaRD Community Advisory Group and prioritised using the APEASE framework. Prioritised interventions targeted a range of stakeholders and included creating a lived experience video library, supporting peer support groups with grant applications, and educating clinicians about referring to peer support groups. Further research is now required to test these findings before trialling and evaluating an intervention to measure the impact on the GUaRD community.</description><identifier>ISSN: 1868-310X</identifier><identifier>ISSN: 1868-6001</identifier><identifier>EISSN: 1868-6001</identifier><identifier>DOI: 10.1007/s12687-023-00643-1</identifier><identifier>PMID: 37000401</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Epidemiology ; Gene Function ; Gene Therapy ; Genetic analysis ; Human Genetics ; Peer tutoring ; Public Health ; Rare diseases ; Support groups</subject><ispartof>Journal of community genetics, 2023-06, Vol.14 (3), p.295-305</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://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><cites>FETCH-LOGICAL-c370t-22c3de6e86093d424febb3a9fd2883743fcb0e4ccb377ee4e08d435a61af9f8d3</cites><orcidid>0000-0002-1107-8976</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37000401$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beadell, Inez</creatorcontrib><creatorcontrib>Byun, Malia</creatorcontrib><creatorcontrib>Feller, Hollie</creatorcontrib><creatorcontrib>Ferrie, Monica</creatorcontrib><creatorcontrib>Best, Stephanie</creatorcontrib><title>Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community</title><title>Journal of community genetics</title><addtitle>J Community Genet</addtitle><addtitle>J Community Genet</addtitle><description>The Genetic, Undiagnosed and Rare Disease community faces a range of hurdles to live their ‘best life’ including physical, social and psychological barriers. They are also resilient and experiential experts with insight into what works and what could work for them. In this study, we aimed to identify and prioritise practical interventions the Genetic, Undiagnosed and Rare Disease community report could help them to ‘live well’. Using a three-stage approach, we first analysed data from a year-long Genetic, Undiagnosed and Rare Disease journal study to record all the practical interventions reported, either trialled or proposed. Second, after grouping the interventions (
n
= 19) into four themes (support for individuals with GUaRD; support for carers of people with GUaRD; education/employment; transition), we presented the interventions to members of the GUaRD community (people with GUaRD, their carers and peer support group members) across three focus groups (
n
= 13). Focus group transcripts were analysed for refinements to the interventions, barriers and/or enablers to enacting them and for any additional interventions suggested. From this analysis, the interventions were grouped to identify specific actionable activities (
n
= 8). Finally, these eight interventions were discussed in a workshop with the GUaRD Community Advisory Group and prioritised using the APEASE framework. Prioritised interventions targeted a range of stakeholders and included creating a lived experience video library, supporting peer support groups with grant applications, and educating clinicians about referring to peer support groups. Further research is now required to test these findings before trialling and evaluating an intervention to measure the impact on the GUaRD community.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Epidemiology</subject><subject>Gene Function</subject><subject>Gene Therapy</subject><subject>Genetic analysis</subject><subject>Human Genetics</subject><subject>Peer tutoring</subject><subject>Public Health</subject><subject>Rare diseases</subject><subject>Support groups</subject><issn>1868-310X</issn><issn>1868-6001</issn><issn>1868-6001</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kUFrFDEUx4MottR-AQ8S8FLB0SRvNpPxVra6CgWhuOAtZJI3a8pOsiYz1d569Rvo1-snMXZWBQ_mkjzye_-88CPkMWcvOGPNy8yFVE3FBFSMyRoqfo8cciVVJRnj9_dn4OzjATnO-ZKVBcAXcvGQHEBTqprxQ_JtGSuH2W-CDxvqw4jpCsPoY8h0jPT25vvWXyH9gtvt7c2PVxS_7jB5DBYzNcHRUlnczXzs6fgJ6QoDjt4-p-vgvNmEmNHdsRcmIT3zGU1GerJam4uzZ9TGYZiCH68fkQe92WY83u9HZP3m9Yfl2-r8_erd8vS8smXqsRLCgkOJSrIWXC3qHrsOTNs7oRQ0NfS2Y1hb20HTINbIlKthYSQ3fdsrB0fkZM7dpfh5wjzqwWdb_mcCxilr0bTQKtlyUdCn_6CXcUqhTKeFEhLUom2hUGKmbIo5J-z1LvnBpGvNmf7lSs-udHGl71xpXpqe7KOnbkD3p-W3mQLADORyFTaY_r79n9ifGhChrw</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Beadell, Inez</creator><creator>Byun, Malia</creator><creator>Feller, Hollie</creator><creator>Ferrie, Monica</creator><creator>Best, Stephanie</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1107-8976</orcidid></search><sort><creationdate>20230601</creationdate><title>Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community</title><author>Beadell, Inez ; Byun, Malia ; Feller, Hollie ; Ferrie, Monica ; Best, Stephanie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-22c3de6e86093d424febb3a9fd2883743fcb0e4ccb377ee4e08d435a61af9f8d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Epidemiology</topic><topic>Gene Function</topic><topic>Gene Therapy</topic><topic>Genetic analysis</topic><topic>Human Genetics</topic><topic>Peer tutoring</topic><topic>Public Health</topic><topic>Rare diseases</topic><topic>Support groups</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beadell, Inez</creatorcontrib><creatorcontrib>Byun, Malia</creatorcontrib><creatorcontrib>Feller, Hollie</creatorcontrib><creatorcontrib>Ferrie, Monica</creatorcontrib><creatorcontrib>Best, Stephanie</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of community genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beadell, Inez</au><au>Byun, Malia</au><au>Feller, Hollie</au><au>Ferrie, Monica</au><au>Best, Stephanie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community</atitle><jtitle>Journal of community genetics</jtitle><stitle>J Community Genet</stitle><addtitle>J Community Genet</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>14</volume><issue>3</issue><spage>295</spage><epage>305</epage><pages>295-305</pages><issn>1868-310X</issn><issn>1868-6001</issn><eissn>1868-6001</eissn><abstract>The Genetic, Undiagnosed and Rare Disease community faces a range of hurdles to live their ‘best life’ including physical, social and psychological barriers. They are also resilient and experiential experts with insight into what works and what could work for them. In this study, we aimed to identify and prioritise practical interventions the Genetic, Undiagnosed and Rare Disease community report could help them to ‘live well’. Using a three-stage approach, we first analysed data from a year-long Genetic, Undiagnosed and Rare Disease journal study to record all the practical interventions reported, either trialled or proposed. Second, after grouping the interventions (
n
= 19) into four themes (support for individuals with GUaRD; support for carers of people with GUaRD; education/employment; transition), we presented the interventions to members of the GUaRD community (people with GUaRD, their carers and peer support group members) across three focus groups (
n
= 13). Focus group transcripts were analysed for refinements to the interventions, barriers and/or enablers to enacting them and for any additional interventions suggested. From this analysis, the interventions were grouped to identify specific actionable activities (
n
= 8). Finally, these eight interventions were discussed in a workshop with the GUaRD Community Advisory Group and prioritised using the APEASE framework. Prioritised interventions targeted a range of stakeholders and included creating a lived experience video library, supporting peer support groups with grant applications, and educating clinicians about referring to peer support groups. Further research is now required to test these findings before trialling and evaluating an intervention to measure the impact on the GUaRD community.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37000401</pmid><doi>10.1007/s12687-023-00643-1</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-1107-8976</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Epidemiology Gene Function Gene Therapy Genetic analysis Human Genetics Peer tutoring Public Health Rare diseases Support groups |
title | Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community |
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