An under-represented and underserved population in trials: methodological, structural, and systemic barriers to the inclusion of adults lacking capacity to consent by Victoria Shepherd

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Decision-Making During Pandemics and Other Serious Illness by Victoria Shepherd

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(Re)Conceptualising ‘good’ proxy decision-making for research: the implications for proxy consent decision quality by Victoria Shepherd

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Exploring the inclusion of under-served groups in trials methodology research: an example from ethnic minority populations’ views on deferred consent by Timia Raven-Gregg, Victoria Shepherd

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Effective approaches to public involvement in care home research: a systematic review and narrative synthesis by Tanisha Burgher, Victoria Shepherd, Claire Nollett

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‘It’s not making a decision, it’s prompting the discussions’: a qualitative study exploring stakeholders’ views on the acceptability and feasibility of advance research planning (C... by Victoria Shepherd, Kerenza Hood, Fiona Wood

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Determining capacity of people with dementia to take part in research: an electronic survey study of researcher confidence, competence and training needs by Sarah Griffiths, Victoria Shepherd, Anna Volkmer

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Planning ahead for research participation: survey of public and professional stakeholders’ views about the acceptability and feasibility of advance research planning by Victoria Shepherd, Kerenza Hood, Fiona Wood

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Trials using deferred consent in the emergency setting: a systematic review and narrative synthesis of stakeholders’ attitudes by Aran Fitzpatrick, Fiona Wood, Victoria Shepherd

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Unpacking the ‘black box of horrendousness’: a qualitative exploration of the barriers and facilitators to conducting trials involving adults lacking capacity to consent by Victoria Shepherd, Kerenza Hood, Fiona Wood

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Development of a measure to assess the quality of proxy decisions about research participation on behalf of adults lacking capacity to consent: the Combined Scale for Proxy Informe... by Victoria Shepherd, Kerenza Hood, Katie Gillies, Fiona Wood

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Identifying barriers and facilitators to the inclusion of older adults living in UK care homes in research: a scoping review by Brittany Nocivelli, Victoria Shepherd, Kerenza Hood, Carolyn Wallace, Fiona Wood

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Nocebo effects and participant information leaflets: evaluating information provided on adverse effects in UK clinical trials by Nigel Kirby, Victoria Shepherd, Jeremey Howick, Sophie Betteridge, Kerenza Hood

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Protection by exclusion? The (lack of) inclusion of adults who lack capacity to consent to research in clinical trials in the UK by Victoria Shepherd, Fiona Wood, Richard Griffith, Mark Sheehan, Kerenza Hood

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Research involving adults lacking capacity to consent: a content analysis of participant information sheets for consultees and legal representatives in England and Wales by Victoria Shepherd, Fiona Wood, Richard Griffith, Mark Sheehan, Kerenza Hood

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Development of a decision support intervention for family members of adults who lack capacity to consent to trials by Victoria Shepherd, Fiona Wood, Richard Griffith, Mark Sheehan, Kerenza Hood

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Conducting focus groups in neurodegenerative disease populations: ethical and methodological considerations by Annabel Jones, Fiona Wood, Monica Busse, Philippa Morgan-Jones, Victoria Shepherd

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Recruitment interventions for trials involving adults lacking capacity to consent: methodological and ethical considerations for designing Studies Within a Trial (SWATs) by Victoria Shepherd, Fiona Wood, Katie Gillies, Abby O’Connell, Adam Martin, Kerenza Hood

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Feasibility, effectiveness and costs of a decision support intervention for consultees and legal representatives of adults lacking capacity to consent (CONSULT): protocol for a ran... by Victoria Shepherd, Fiona Wood, Katie Gillies, Adam Martin, Abby O’Connell, Kerenza Hood

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Impact of a deferred recruitment model in a randomised controlled trial in primary care (CREAM study) by Victoria Shepherd, Emma Thomas-Jones, Matthew J. Ridd, Kerenza Hood, Katy Addison, Nick A. Francis

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