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The Patient|December 12, 2023
Current Practices and Challenges When Submitting Patient Experience Data for Regulatory Decisions by the US Food and Drug Administration: An Industry SurveyCathy Anne Pinto, Tommi Tervonen, Cecilia Jimenez-Moreno, et al.
The Patient|December 7, 2023
Quality of Life in Adults with Chronic Cough: A Mixed Methods Study Informing the Development of a Quantitative Patient Preference StudyTheresa Coles, Molly McFatrich, Helen Ding, et al.
The Patient|October 24, 2023
Role Preferences in Medical Decision Making: Relevance and Implications for Health Preference ResearchJanine A van Til, Alison Pearce, Semra Ozdemir, et al.
The Patient|November 7, 2019
Patient Perspectives on Novel Treatments in Haemophilia: A Qualitative StudyErna C van Balen, Marjolein L Wesselo, Bridget L Baker, et al.
The Patient|December 21, 2019
Development and Content Validity Testing of Patient-Reported Outcome Items for Children to Self-Assess Symptoms of the Common ColdPatricia Halstead, Rob Arbuckle, Chris Marshall, et al.
The Patient|December 6, 2019
Tapering Biologic Therapy for Rheumatoid Arthritis: A Qualitative Study of Patient PerspectivesSuz Jack Chan, Lisa K Stamp, Nicola Liebergreen, et al.
The Patient|February 20, 2020
The Economic Impact on Australian Patients with Neuroendocrine TumoursLouisa G Gordon, Thomas M Elliott, Kate Wakelin, et al.
The Patient|November 5, 2020
What Factors Influence Non-Participation Most in Colorectal Cancer Screening? A Discrete Choice ExperimentEsther W de Bekker-Grob, Bas Donkers, Jorien Veldwijk, et al.
The Patient|October 19, 2020
Utility Values for the CP-6D, a Cerebral Palsy-Specific Multi-Attribute Utility Instrument, Using a Discrete Choice ExperimentMina Bahrampour, Richard Norman, Joshua Byrnes, et al.
The Patient|September 27, 2020
Empirical Validity of a Generic, Preference-Based Capability Wellbeing Instrument (ICECAP-A) in the Context of Spinal Cord InjuryCassandra Mah, Vanessa K Noonan, Stirling Bryan, et al.
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