668 results on '"Bridges, John F. P."'
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2. Prioritization of ethical concerns regarding HIV molecular epidemiology by public health practitioners and researchers
3. Barriers to diverse clinical trial participation in Duchenne muscular dystrophy: Engaging Hispanic/Latina caregivers and health professionals
4. Pretesting Discrete-Choice Experiments: A Guide for Researchers
5. Experiences of treatment decision-making among older newly diagnosed adults with acute myeloid leukemia: a qualitative descriptive study
6. Increasing Access to Buprenorphine for Opioid Use Disorder in Primary Care: an Assessment of Provider Incentives
7. Rethinking Patient Engagement in Cancer Research
8. Best–Worst Scaling and the Prioritization of Objects in Health: A Systematic Review
9. A Comparison of Caregiver and Patient Preferences for Treating Duchenne Muscular Dystrophy
10. Unmet Therapeutic Needs of Non-Ambulatory Patients with Duchenne Muscular Dystrophy: A Mixed-Method Analysis
11. Comparing Patient Preferences for Antithrombotic Treatment During the Acute and Chronic Phases of Myocardial Infarction: A Discrete-Choice Experiment
12. Public Perspectives on Multi-Cancer Early Detection: A Qualitative Study.
13. Assessing the Benefits and Harms Associated with Early Diagnosis from the Perspective of Parents with Multiple Children Diagnosed with Duchenne Muscular Dystrophy
14. Willingness and preferences for long-acting injectable PrEP among US men who have sex with men: a discrete choice experiment
15. The impact of metabolic syndrome severity on racial and ethnic disparities in Metabolic Dysfunction-Associated Steatotic Liver Disease
16. Parent clinical trial priorities for fragile X syndrome: a best–worst scaling
17. Patient experience and quality of life during neoadjuvant therapy for pancreatic cancer: a systematic review and study protocol
18. Eliciting Preferences for HIV Prevention Technologies: A Systematic Review
19. Home Time Among Older Adults With Acute Myeloid Leukemia Following Chemotherapy.
20. Comparing the Preferences of Patients and the General Public for Treatment Outcomes in Type 2 Diabetes Mellitus
21. OP87 A Roadmap for Increasing The Usefulness And Impact Of Patient Preference Studies In Health Technology Assessment (HTA)
22. A best–worst scaling experiment to prioritize concern about ethical issues in citizen science reveals heterogeneity on people-level v. data-level issues
23. Do people have differing motivations for participating in a stated-preference study? Results from a latent-class analysis
24. Advancing the Use of Patient Preference Information as Scientific Evidence in Medical Product Evaluation: A Summary Report of the Patient Preference Workshop
25. Engaging patients and caregivers in prioritizing symptoms impacting quality of life for Duchenne and Becker muscular dystrophy
26. Discussion: Research to Promote Patient-Based HTA
27. Maternal Motivation to Take Preventive Therapy in Antepartum and Postpartum Among HIV-Positive Pregnant Women in South Africa: A Choice Experiment
28. How Do Members of the Duchenne and Becker Muscular Dystrophy Community Perceive a Discrete-Choice Experiment Incorporating Uncertain Treatment Benefit? An Application of Research as an Event
29. Preferences for antiviral therapy of chronic hepatitis C: a discrete choice experiment
30. Promoting patient engagement in cancer genomics research programs: An environmental scan
31. Correction to: Comparing the Preferences of Patients and the General Public for Treatment Outcomes in Type 2 Diabetes Mellitus
32. Increasing Access to Buprenorphine for Opioid Use Disorder in Primary Care: an Assessment of Provider Incentives
33. Using Latent Class Analysis to Model Preference Heterogeneity in Health: A Systematic Review
34. Identifying and Prioritizing the Barriers and Facilitators to the Self-Management of Type 2 Diabetes Mellitus: A Community-Centered Approach
35. A Latent Class Analysis to Identify Variation in Caregivers’ Preferences for their Child’s Attention-Deficit/Hyperactivity Disorder Treatment: Do Stated Preferences Match Current Treatment?
36. An international comparison of stakeholder motivation to implement liver cancer control
37. An Index for Measuring Overuse of Health Care Resources With Medicare Claims
38. Using Best–Worst Scaling to Investigate Preferences in Health Care
39. Rethinking Patient Engagement in Cancer Research
40. Expanding the E-Liquid Flavor Wheel: Classification of Emerging E-Liquid Flavors in Online Vape Shops
41. Association of Bariatric Surgery With Cardiovascular Outcomes in Adults With Severe Obesity and Nonalcoholic Fatty Liver Disease
42. Caregiversʼ Priorities and Observed Outcomes of Attention-Deficit Hyperactivity Disorder Medication for Their Children
43. A review of paper-based advance care planning aids
44. Art and Science of Instrument Development for Stated-Preference Methods
45. A Framework for Instrument Development of a Choice Experiment: An Application to Type 2 Diabetes
46. Understanding the Experience of Age-Related Vestibular Loss in Older Individuals: A Qualitative Study
47. Perceived Barriers and Potential Strategies to Improve Self-Management Among Adults with Type 2 Diabetes: A Community-Engaged Research Approach
48. Variation in Treatment Priorities for Chronic Hepatitis C: A Latent Class Analysis
49. Patient Preferences for Injectable Treatments for Multiple Sclerosis in the United States: A Discrete-Choice Experiment
50. Guidelines for Artificial Intelligence in Medicine: Literature Review and Content Analysis of Frameworks
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