Wendy O Baird

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Public Involvement in the Design and Conduct of Clinical Trials

J. Boote, A. Sutton, Wendy O Baird, 2011 .

Conducting qualitative research within Clinical Trials Units: avoiding potential pitfalls.

A. O’Cathain, J. Adamson, C. Cooper, 2014, Contemporary clinical trials.

Abstracts from the NIHR INVOLVE Conference 2017

Michael Nunns, Sara Schroter, Jenny Donovan, 2017, Research Involvement and Engagement.

Public involvement in the systematic review process in health and social care: a narrative review of case examples.

J. Boote, A. Sutton, Wendy O Baird, 2011, Health policy.

Public involvement in the design and conduct of clinical trials: a narrative review of case examples

J. Boote, A. Sutton, Wendy O Baird, 2011, Trials.

The TiM system: developing a novel telehealth service to improve access to specialist care in motor neurone disease using user-centered design

S. Mawson, C. Cooper, P. Shaw, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Conducting qualitative research within Clinical Trials Units

A. O’Cathain, J. Adamson, D. Hind, 2014 .

Involving the public in systematic reviews: a narrative review of organizational approaches and eight case examples.

J. Boote, A. Sutton, Wendy O Baird, 2012, Journal of comparative effectiveness research.

Supporting public involvement in interview and other panels: a systematic review

S. Baxter, Wendy O Baird, D. Muir, 2016, Health expectations : an international journal of public participation in health care and health policy.

Evaluating public involvement in research design and grant development: Using a qualitative document analysis method to analyse an award scheme for researchers

B. Hodges, L. Brereton, S. Baxter, 2016, Research Involvement and Engagement.

Safety and efficacy of diaphragm pacing in patients with respiratory insufficiency due to amyotrophic lateral sclerosis (DiPALS): a multicentre, open-label, randomised controlled trial

A. Simonds, R. Orrell, M. Dewey, 2015, The Lancet Neurology.

Supporting public involvement in research design and grant development: a case study of a public involvement award scheme managed by a National Institute for Health Research (NIHR) Research Design Service (RDS)

J. Boote, M. Twiddy, D. Beever, 2015, Health expectations : an international journal of public participation in health care and health policy.

The impact of gastrostomy in motor neurone disease: challenges and benefits from a patient and carer perspective

P. Shaw, T. Stavroulakis, C. Mcdermott, 2014, BMJ Supportive & Palliative Care.

Protocol for diaphragm pacing in patients with respiratory muscle weakness due to motor neurone disease (DiPALS): a randomised controlled trial

S. Dixon, J. Stradling, M. Bradburn, 2012, BMC Neurology.

DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis - a randomised controlled trial.

A. Simonds, S. Dixon, J. Stradling, 2016, Health technology assessment.

Quality of life in children and adolescents with Osteogenesis Imperfecta: a qualitative interview based study

S. Walters, Wendy O Baird, Claire L. Hill, 2014, Health and Quality of Life Outcomes.

Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre

S. Mawson, M. Bradburn, C. Cooper, 2019, BMJ Open.

Public involvement at the design stage of primary health research: a narrative review of case examples.

Jonathan Boote, Claire Beecroft, J. Boote, 2010, Health policy.

Development of an osteogenesis imperfecta (OI) specific quality of life measure (OIQoL)

S. Walters, Wendy O Baird, C. Hill, 2016 .

Can an Emergency Department-based Clinical Decision Unit successfully utilize alternatives to emergency hospitalization?

Seamus O’Reilly, Wendy O Baird, Wendy Baird, 2010, European journal of emergency medicine : official journal of the European Society for Emergency Medicine.

Protocol for a cluster randomised controlled trial of the DAFNEplus (Dose Adjustment For Normal Eating) intervention compared with 5x1 DAFNE: a lifelong approach to promote effective self-management in adults with type 1 diabetes

Mohammad R. Eissa, A. Brennan, T. Good, 2021, BMJ Open.

Use of the h-index to measure the quality of the output of health services researchers

Marion Campbell, Yvonne Birks, Caroline Fairhurst, 2014, Journal of health services research & policy.

The use of the h-index to measure quality and output: A bibliometric analysis in health service research.

D. Torgerson, C. Fairhurst, M. Campbell, 2014 .

The impact on the family carer of motor neurone disease and intervention with noninvasive ventilation.

P. Shaw, S. Walters, C. Mcdermott, 2013, Journal of palliative medicine.

Factors influencing decision-making in relation to timing of gastrostomy insertion in patients with motor neurone disease

P. Shaw, T. Stavroulakis, C. Mcdermott, 2013, BMJ Supportive & Palliative Care.

The use of non-invasive ventilation at end of life in patients with motor neurone disease: A qualitative exploration of family carer and health professional experiences

S. Walters, C. Mcdermott, S. Baxter, 2013, Palliative medicine.

Using telehealth in motor neuron disease to increase access to specialist multidisciplinary care: a UK-based pilot and feasibility study

S. Mawson, M. Bradburn, C. Cooper, 2019, BMJ Open.

Delphi research: issues raised by a pilot study.

Wendy O Baird, S. Walters, Nicola Clibbens, 2012, Nurse researcher.

The initiation of non-invasive ventilation for patients with motor neuron disease: Patient and carer perceptions of obstacles and outcomes

P. Shaw, S. Walters, C. Mcdermott, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Using technology to improve access to specialist care in amyotrophic lateral sclerosis: A systematic review

S. Mawson, C. Cooper, C. Mcdermott, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Factors influencing decision-making in relation to timing of gastrostomy insertion in patients with motor neurone disease

T. Stavroulakis, C. Mcdermott, S. Baxter, 2013, BMJ Supportive & Palliative Care.