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Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial
BACKGROUND: Despite methodological improvements in clinical trial design and conduct more generally, methodological limitations persist in trials concerning mental health care. A qualitative Study Within A Trial (Qual-SWAT), embedded in the KARMA-Dep-2 host trial, will be undertaken to explore and g...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285324/ https://www.ncbi.nlm.nih.gov/pubmed/37361338 http://dx.doi.org/10.12688/hrbopenres.13721.2 |
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author | McCaffrey, John Terao, Masashi McCaffrey, Cathal Igoe, Anna Loughran, Orlaith McDonagh, Kelly McDonogh, Sarah Shackleton, Ellie Whooley, Emma Jelovac, Ana McLoughlin, Declan M. Hunter, Andrew |
author_facet | McCaffrey, John Terao, Masashi McCaffrey, Cathal Igoe, Anna Loughran, Orlaith McDonagh, Kelly McDonogh, Sarah Shackleton, Ellie Whooley, Emma Jelovac, Ana McLoughlin, Declan M. Hunter, Andrew |
author_sort | McCaffrey, John |
collection | PubMed |
description | BACKGROUND: Despite methodological improvements in clinical trial design and conduct more generally, methodological limitations persist in trials concerning mental health care. A qualitative Study Within A Trial (Qual-SWAT), embedded in the KARMA-Dep-2 host trial, will be undertaken to explore and gain an understanding of two methodological questions in randomised trials specific to mental health care: (1) what are the key barriers and enablers of participation in randomised trials in mental health; and (2) how can randomised trials become part of routine mental health care. These issues will be examined from patient-participant and clinician- / researcher-participant perspectives, in alignment with PRioRiTy research themes. METHODS: A descriptive qualitative study design will be used. Data will be collected via one-to-one semi-structured interviews, conducted via Microsoft Teams. The interview data will be analysed using Braun and Clarke’s Thematic Analysis approach. One-to-one interviews will be conducted with three participant groups ( N = 30): 1) host trial patient-participants ( n = 10); 2) potentially eligible host trial patient-participants who refused enrolment in the host trial ( n = 10); and 3) clinician- / researcher-participants who are associated with work on the host trial ( n = 10). ETHICS AND DISSEMINATION: Ethical approval has been granted by St. Patrick’s Mental Health Services Research Ethics Committee, Ireland (Ref: Protocol 09/20). When the study is completed, a report will be prepared and submitted to the Health Research Board (HRB). Findings will be shared with the host trial team and study participants, and submitted for publication. HOST TRIAL REGISTRATION: ClinicalTrials.gov ( NCT04939649); EudraCT ( 2019-003109-92). Official title: Ketamine as an Adjunctive Therapy for Major Depression - A Randomised Controlled Trial: [KARMA-Dep (2)]. |
format | Online Article Text |
id | pubmed-10285324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-102853242023-11-20 Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial McCaffrey, John Terao, Masashi McCaffrey, Cathal Igoe, Anna Loughran, Orlaith McDonagh, Kelly McDonogh, Sarah Shackleton, Ellie Whooley, Emma Jelovac, Ana McLoughlin, Declan M. Hunter, Andrew HRB Open Res Study Protocol BACKGROUND: Despite methodological improvements in clinical trial design and conduct more generally, methodological limitations persist in trials concerning mental health care. A qualitative Study Within A Trial (Qual-SWAT), embedded in the KARMA-Dep-2 host trial, will be undertaken to explore and gain an understanding of two methodological questions in randomised trials specific to mental health care: (1) what are the key barriers and enablers of participation in randomised trials in mental health; and (2) how can randomised trials become part of routine mental health care. These issues will be examined from patient-participant and clinician- / researcher-participant perspectives, in alignment with PRioRiTy research themes. METHODS: A descriptive qualitative study design will be used. Data will be collected via one-to-one semi-structured interviews, conducted via Microsoft Teams. The interview data will be analysed using Braun and Clarke’s Thematic Analysis approach. One-to-one interviews will be conducted with three participant groups ( N = 30): 1) host trial patient-participants ( n = 10); 2) potentially eligible host trial patient-participants who refused enrolment in the host trial ( n = 10); and 3) clinician- / researcher-participants who are associated with work on the host trial ( n = 10). ETHICS AND DISSEMINATION: Ethical approval has been granted by St. Patrick’s Mental Health Services Research Ethics Committee, Ireland (Ref: Protocol 09/20). When the study is completed, a report will be prepared and submitted to the Health Research Board (HRB). Findings will be shared with the host trial team and study participants, and submitted for publication. HOST TRIAL REGISTRATION: ClinicalTrials.gov ( NCT04939649); EudraCT ( 2019-003109-92). Official title: Ketamine as an Adjunctive Therapy for Major Depression - A Randomised Controlled Trial: [KARMA-Dep (2)]. F1000 Research Limited 2023-11-20 /pmc/articles/PMC10285324/ /pubmed/37361338 http://dx.doi.org/10.12688/hrbopenres.13721.2 Text en Copyright: © 2023 McCaffrey J et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Study Protocol McCaffrey, John Terao, Masashi McCaffrey, Cathal Igoe, Anna Loughran, Orlaith McDonagh, Kelly McDonogh, Sarah Shackleton, Ellie Whooley, Emma Jelovac, Ana McLoughlin, Declan M. Hunter, Andrew Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial |
title | Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial |
title_full | Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial |
title_fullStr | Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial |
title_full_unstemmed | Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial |
title_short | Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial |
title_sort | protocol development for a qualitative methodological study within a trial (qual-swat): the karma-dep-2 trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285324/ https://www.ncbi.nlm.nih.gov/pubmed/37361338 http://dx.doi.org/10.12688/hrbopenres.13721.2 |
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