Dr Rebecca Walwyn
- Position: Acting Associate Professor of Clinical Trials Methodology
- Areas of expertise: Design and analysis of complex intervention trials; treatment-related clustering; early-phase trial design; cluster-randomised trial design; factorial trial design; design of experiments
- Email: R.E.A.Walwyn@leeds.ac.uk
- Phone: +44(0)113 343 5485
- Location: 10.79, Level 10, Worsley Building
- Website: ORCID
Associate Professor of Clinical Trials Methodology, Rebecca is the main point of contact in LICTR for teaching, trial and statistical methodology related queries. She joined the Complex Interventions Division in the Clinical Trials Research Unit at Leeds in January 2011. Her time is split equally between teaching and research. She leads the weekly LICTR Methodology Meetings. Rebecca was previously a statistician at the Institute of Psychiatry, King’s College London from 2001 to 2010, initially in the Department of Biostatistics and Computing and then from 2003 in the Mental Health and Neuroscience Clinical Trials Unit. During this time she worked for the Sainsbury Centre for Mental Health (2001-2002), completed a PhD at University of Manchester (MRC fellowship, 2006-2010) and was seconded to the MRC CTU (2009-2010).
2019 – 2020: Reducing self-harm in adolescents: Individual patient data meta-analysis. Co-Investigator with PI David Cottrell (NIHR HTA).
2018 – 2023: Trial design and analysis to incorporate the complexities of surgery. Supervisor for PI Neil Corrigan (NIHR Doctoral Fellowship)
2018 – 2020: Open-cohort designs for cluster-randomised trials in institutional settings: A methodology bolt-on to DCM-EPIC. Principal Investigator (MRC).
2017 – 2020: Improving the outputs of national clinical audits to support organisations to improve the quality of care and clinical outcomes. Co-Investigator with PI Robbie Foy (NIHR HS&DR).
2016 – 2019: Novel clinical trial designs for establishing potential efficacy of complex interventions. Sponsor for PI Duncan Wilson (MRC Skills Development Fellowship)
2015 – 2017: TIGA-CUB (Feasibility study for a trial on improving inter-generational attachment for children undergoing behavioural problems). Co-Investigator with PI Elizabeth Edginton (NIHR RfPB).
2013 – 2017: DCM-EPIC (Evaluating the effectiveness and cost effectiveness of Dementia Care Mapping (DCM) to enable person-centred care for people with dementia and carers: A cluster randomised controlled trial in care homes). Co-Investigator with PI Claire Surr (NIHR HTA).
2013 – 2018: AFFINITIE (The development and evaluation of enhanced audit and feedback interventions to increase the uptake of evidence-based transfusion practice). Supervising statistician with PI Simon Stanworth (NIHR PGfAR).
2013 – 2015: Early-phase complex intervention trials. Methodologist for Duncan Wilson (NIHR Research Methods Fellowship).
2012 – 2016: OK-DIABETES (Managing with learning disability and diabetes). Supervising statistician with PI Allan House (NIHR HTA).
2011 – 2013: IMPROVE-PC (A randomised feasibility trial of systematic lifestyle referral assessment compared to standard assessment in an acute cardiology service). Trial statistician with PI Allan House (CLAHRC).
2006 – 2010: Therapist effects in the design, analysis and reporting of psychotherapy randomised clinical trials. Principal Investigator (MRC Special Training Fellowship in HSR).
2005 – 2011: HTA-SADD (HTA study of antidepressants for depression in dementia). Co-Investigator with PI Sube Banerjee (NIHR HTA).
2003 – 2005: FEVER (Flu: effectiveness of vaccine in elderly residents). Co-Investigator with PI Fiona Gaughran (Guy’s & St. Thomas’ Charitable Foundation).
2003 – 2010: PACE (Pacing, graded activity, and cognitive behaviour therapy; a randomised evaluation). Trial/supervising statistician with PI Peter White (MRC).
2003 – 2009: HSEN (A double-blind placebo-controlled trial of methylphenidate among children with moderate and severe learning disabilities). Trial/supervising statistician with PI Emily Simonoff (PPP Foundation).
Champion for International Biometrics Society
Member of HQIP Methodology Advisory Group
- Director of Student Education
- Deputy Postgraduate Tutor
From a methodological perspective, Rebecca is interested in maximising the efficiency of, and information obtained from, clinical trials of complex interventions, such as, but not restricted to, psychotherapy. Within this broad area she is interested in treatment-related clustering (e.g. ‘therapist effects’) in trials, meta-analyses and observational data. More recently, her interests have extended to novel experimental designs (e.g. split-block designs, split-plot designs, multi-tiered designs, conditional randomisations, open-cohort cluster-randomised trial designs) and combinations of those designs, building on Design of Experiments (DoE). She is also interested in the role of time in trials of complex interventions. From a trials perspective, Rebecca is interested in building a portfolio of trials that evaluate psychological interventions and audit and feedback, particularly in a mental health setting. However, she has developed an interest in all types of complex intervention, where her interest is in supporting the implementation of innovative trial designs across the Clinical Trials Research Unit.
2016 - 2018: Pritaporn Kingkaew (co-supervisor: Glidewell, Wyatt): Optimising the development of effective mobile health behaviour change interventions
2016 - 2021: Richard Wilkins (co-supervisor: Redmond, Chapman, Horn, Siddle): Haemarthrosis of the ankle in haemophilia A and B: Prevalence, impact and intervention
2018 - 2023: Neil Corrigan (co-supervisor: Brown, Emsley): Trial design and analysis to incorporate the complexities of surgery
2018 - 2021: Laura Marsden (co-supervisor: Copas, Farrin): Open-cohort designs for cluster-randomised trials in institutional settings
- BSc Psychology (University of Kent at Canterbury, 1996-1999)
- MSc Social Statistics (University of Southampton, 1999-2001)
- PhD Biostatistics (University of Manchester, 2006-2010)
Rebecca is the Director of Student Education for LICTR and a Deputy Postgraduate Tutor for LIHS/LICTR with primary responsibility for LICTR. She is co-module lead for RESS1 (MBChB, Year 1) “Research, Evaluation and Special Studies”, MEDR5320M (Certificate in Health Research) "Capturing and Handling Data for Research" and MEDR5130M (Certificate in Health Research) "Intervention Research".
Research groups and institutes
- Leeds Institute of Clinical Trials Research