Identifying outcomes for depression that matter to patients, informal caregivers, and health-care professionals: qualitative content analysis of a large international online survey
- PMID: 32711710
- DOI: 10.1016/S2215-0366(20)30191-7
Identifying outcomes for depression that matter to patients, informal caregivers, and health-care professionals: qualitative content analysis of a large international online survey
Erratum in
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Correction to Lancet Psychiatry 2020; 7: 692-702.Lancet Psychiatry. 2020 Sep;7(9):e59. doi: 10.1016/S2215-0366(20)30351-5. Lancet Psychiatry. 2020. PMID: 32828169 No abstract available.
Abstract
Background: Many clinical trials have assessed treatments for depressive disorders and bipolar depression. However, whether, and which, assessed outcome domains really matter to patients, informal caregivers, and health-care professionals remains unclear.
Methods: We did an international online survey in French, German, and English. Participants were adult patients with a history of depression, informal caregivers, and health-care professionals, recruited by purposeful sampling. To identify outcome domains, participants answered four open-ended questions about their expectations for depression treatment. We disseminated the survey without restriction via social media, patient and professional associations, and a media campaign. Four researchers independently did qualitative content analyses. We assessed data saturation using mathematical models to ensure the comprehensive identification of outcome domains.
Findings: Between April 5, 2018, and Dec 10, 2018, 1912 patients, 464 informal caregivers, and 627 health-care professionals from 52 countries provided 8183 open-ended answers. We identified 80 outcome domains related to symptoms (64 domains), such as mental pain (or psychological or psychic pain, 523 [17%] of 3003 participants) and motivation (384 [13%]), and functioning (16 domains), such as social isolation (541 [18%]). We identified 57 other outcome domains regarding safety of treatment, health care organisation, and social representation, such as stigmatisation (408 [14%]).
Interpretation: This study provides a list of outcome domains important to patients, informal caregivers, and health-care professionals. Unfortunately, many of these domains are rarely measured in clinical trials. Results from this study should set the foundation for a core outcome set for depression.
Funding: Fondation pour la Recherche Medicale and NIHR Oxford Health Biomedical Research Centre.
Copyright © 2020 Elsevier Ltd. All rights reserved.
Comment in
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Asking the right questions.Lancet Psychiatry. 2020 Aug;7(8):647. doi: 10.1016/S2215-0366(20)30302-3. Lancet Psychiatry. 2020. PMID: 32711693 No abstract available.
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A participatory approach to determining outcome measures in people with depression.Lancet Psychiatry. 2020 Aug;7(8):650-652. doi: 10.1016/S2215-0366(20)30257-1. Lancet Psychiatry. 2020. PMID: 32711696 No abstract available.
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