Bridget Young
www.liverpool.ac.uk
0000-0001-6041-9901
University of Liverpool
164 papers found
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Awareness and experiences on core outcome set development and use amongst stakeholders from low- and middle- income countries: An online survey
Bracing Adolescent Idiopathic Scoliosis (BASIS) study – night-time versus full-time bracing in adolescent idiopathic scoliosis: study protocol for a multicentre, randomized controlled trial
Providing multimedia information to children and young people increases recruitment to trials: pre-planned meta-analysis of SWATs
Complex and alternate consent pathways in clinical trials: methodological and ethical challenges encountered by underserved groups and a call to action
Metacognitive beliefs predict test anxiety and examination performance
Assessment of Measures of Head and Neck Lymphedema Following Head and Neck Cancer Treatment: A Systematic Review
Patient-centred outcomes following non-operative treatment or appendicectomy for uncomplicated acute appendicitis in children
Learning from stakeholders to inform good practice guidance on consent to research in intensive care units: a mixed-methods study
Thinking Time, Shifting Goalposts and Ticking Time Bombs: Experiences of Waiting on the Gender Identity Development Service Waiting List
Understanding the perspectives of recruiters is key to improving randomised controlled trial enrolment: a qualitative evidence synthesis
Adapting a social network intervention for use in secondary mental health services using a collaborative approach with service users, carers/supporters and health professionals in the United Kingdom
Engaging children, young people, parents and health professionals in interviews: Using an interactive ranking exercise within the co-design of multimedia websites
Patient and health practitioner views and experiences of a cancer trial before and during COVID-19: qualitative study
The development of theory-informed participant-centred interventions to maximise participant retention in randomised controlled trials
In-depth qualitative interviews identified barriers and facilitators that influenced chief investigators’ use of core outcome sets in randomised controlled trials
Enhancing patient and public contribution in health outcome selection during clinical guideline development: an ethnographic study
Assessing the effectiveness of social network interventions for adults with a diagnosis of mental health problems: a systematic review and narrative synthesis of impact
Patients’ Perspectives on Transforming Clinical Trial Participation: Large Online Vignette-based Survey
Testing times: the association of intolerance of uncertainty and metacognitive beliefs to test anxiety in college students
Heterogeneity in outcome assessment for inflammatory bowel disease in routine clinical practice: a mixed-methods study in a sample of English hospitals
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