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Sociodemographic, mental health, and physical health factors associated with participation within re-contactable mental health cohorts: an investigation of the GLAD Study.
Bright, Steven J; Hübel, Christopher; Young, Katherine S; Bristow, Shannon; Peel, Alicia J; Rayner, Christopher; Mundy, Jessica; Palmos, Alish B; Purves, Kirstin L; Kalsi, Gursharan; Armour, Cherie; Jones, Ian R; Hotopf, Matthew; McIntosh, Andrew M; Smith, Daniel J; Walters, James T R; Rogers, Henry C; Thompson, Katherine N; Adey, Brett N; Monssen, Dina; Kakar, Saakshi; Malouf, Chelsea M; Hirsch, Colette; Glen, Kiran; Kelly, Emily J; Veale, David; Eley, Thalia C; Breen, Gerome; Davies, Molly R.
Afiliación
  • Bright SJ; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Hübel C; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Young KS; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Bristow S; Department of Economics and Business Economics, National Centre for Register-Based Research, Aarhus University, Aarhus, Denmark.
  • Peel AJ; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Rayner C; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Mundy J; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Palmos AB; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Purves KL; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Kalsi G; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Armour C; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Jones IR; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Hotopf M; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • McIntosh AM; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Smith DJ; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Walters JTR; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Rogers HC; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Thompson KN; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Adey BN; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Monssen D; Research Centre for Stress, Trauma & Related Conditions (STARC), School of Psychology, Queen's University Belfast (QUB), Belfast, Northern Ireland, UK.
  • Kakar S; Division of Psychiatry and Clinical Neurosciences, National Centre for Mental Health and MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
  • Malouf CM; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Hirsch C; Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Glen K; Division of Psychiatry, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Kelly EJ; Division of Psychiatry, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Veale D; Division of Psychiatry and Clinical Neurosciences, National Centre for Mental Health and MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
  • Eley TC; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
  • Breen G; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Davies MR; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, PO80, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
BMC Psychiatry ; 23(1): 542, 2023 07 26.
Article en En | MEDLINE | ID: mdl-37495971
BACKGROUND: The Genetic Links to Anxiety and Depression (GLAD) Study is a large cohort of individuals with lifetime anxiety and/or depression, designed to facilitate re-contact of participants for mental health research. At the start of the pandemic, participants from three cohorts, including the GLAD Study, were invited to join the COVID-19 Psychiatry and Neurological Genetics (COPING) study to monitor mental and neurological health. However, previous research suggests that participation in longitudinal studies follows a systematic, rather than random, process, which can ultimately bias results. Therefore, this study assessed participation biases following the re-contact of GLAD Study participants. METHODS: In April 2020, all current GLAD Study participants (N = 36,770) were invited to the COPING study. Using logistic regression, we investigated whether sociodemographic, mental, and physical health characteristics were associated with participation in the COPING baseline survey (aim one). Subsequently, we used a zero-inflated negative binomial regression to examine whether these factors were also related to participation in the COPING follow-up surveys (aim two). RESULTS: For aim one, older age, female gender identity, non-binary or self-defined gender identities, having one or more physical health disorders, and providing a saliva kit for the GLAD Study were associated with an increased odds of completing the COPING baseline survey. In contrast, lower educational attainment, Asian or Asian British ethnic identity, Black or Black British ethnic identity, higher alcohol consumption at the GLAD sign-up survey, and current or ex-smoking were associated with a reduced odds. For aim two, older age, female gender, and saliva kit provision were associated with greater COPING follow-up survey completion. Lower educational attainment, higher alcohol consumption at the GLAD Study sign-up, ex-smoking, and self-reported attention deficit hyperactivity disorder had negative relationships. CONCLUSIONS: Participation biases surrounding sociodemographic and physical health characteristics were particularly evident when re-contacting the GLAD Study volunteers. Factors associated with participation may vary depending on study design. Researchers should examine the barriers and mechanisms underlying participation bias in order to combat these issues and address recruitment biases in future studies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 4_TD / 8_ODS3_consumo_sustancias_psicoactivas Problema de salud: 4_pneumonia / 8_alcohol Asunto principal: Salud Mental / COVID-19 Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: BMC Psychiatry Asunto de la revista: PSIQUIATRIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 4_TD / 8_ODS3_consumo_sustancias_psicoactivas Problema de salud: 4_pneumonia / 8_alcohol Asunto principal: Salud Mental / COVID-19 Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: BMC Psychiatry Asunto de la revista: PSIQUIATRIA Año: 2023 Tipo del documento: Article
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