nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Case Study Investigation into the Use of Multi-compartment Compliance Aids in Older People Resident in Very Sheltered Housing
|
MacLure, Katie |
|
2016 |
|
6 |
p. 583-590 |
artikel |
2 |
Acknowledgement to Referees
|
|
|
2016 |
|
6 |
p. 493-494 |
artikel |
3 |
Acknowledgement to Referees
|
|
|
2017 |
|
6 |
p. 669-671 |
artikel |
4 |
Acknowledgement to Referees
|
|
|
2015 |
|
6 |
p. 469-470 |
artikel |
5 |
Acknowledgement to Referees
|
|
|
2018 |
|
6 |
p. 575-576 |
artikel |
6 |
Acknowledgement to Referees
|
|
|
|
|
6 |
p. 551-552 |
artikel |
7 |
A Cross-Sectional Study of the Impact of Spasticity on Daily Activities in Multiple Sclerosis
|
Bethoux, Francois |
|
2016 |
|
6 |
p. 537-546 |
artikel |
8 |
Adapting two American Decision Aids for Mild Traumatic Brain Injury to the Canadian Context Using the Nominal Group Technique
|
Ghandour, El Kebir |
|
|
|
6 |
p. 729-743 |
artikel |
9 |
Advancing the Use of Patient Preference Information as Scientific Evidence in Medical Product Evaluation: A Summary Report of the Patient Preference Workshop
|
Benz, Heather L. |
|
|
|
6 |
p. 553-557 |
artikel |
10 |
A Qualitative Exploration of Patient and Staff Experiences of the Receipt and Delivery of Specialist Weight Management Services in the UK
|
Watkins, Ross |
|
|
|
6 |
p. 625-640 |
artikel |
11 |
Assessing Patient Preferences in Rare Diseases: Direct Preference Elicitation in the Rare Chronic Kidney Disease, Immunoglobulin A Nephropathy
|
Marsh, Kevin |
|
|
|
6 |
p. 837-847 |
artikel |
12 |
Assessing Preference-Based Outcome Measures for Overactive Bladder: An Evaluation of Patient-Reported Outcome Data from the BESIDE Clinical Trial
|
Herdman, Mike |
|
2017 |
|
6 |
p. 677-686 |
artikel |
13 |
Assessing the Impact of Caring for a Person with Schizophrenia: Development of the Schizophrenia Caregiver Questionnaire
|
Gater, Adam |
|
2015 |
|
6 |
p. 507-520 |
artikel |
14 |
A Systematic Review of Discrete Choice Experiments in Oncology Treatments
|
Collacott, Hannah |
|
|
|
6 |
p. 775-790 |
artikel |
15 |
Authors’ Reply to Ibrahim and Nair’s Comment on: “Health Literacy: The Common Denominator of Healthcare Progress”
|
Pitts, Peter J. |
|
|
|
6 |
p. 871 |
artikel |
16 |
Balance Sheets Versus Decision Dashboards to Support Patient Treatment Choices: A Comparative Analysis
|
Dolan, James G. |
|
2015 |
|
6 |
p. 499-505 |
artikel |
17 |
Behavioral Economic Insights to Improve Medication Adherence in Adults with Chronic Conditions: A Scoping Review
|
Roseleur, Jacqueline |
|
|
|
6 |
p. 571-592 |
artikel |
18 |
Best–Worst Scaling Study to Identify Complications Patients Want to Be Informed About Prior to Abdominal Aortic Aneurysm Surgery
|
de Mik, Sylvana M. L. |
|
|
|
6 |
p. 699-707 |
artikel |
19 |
Choosing a Doctor: Does Presentation Format Affect the Way Consumers Use Health Care Performance Information?
|
Kenny, Patricia |
|
2017 |
|
6 |
p. 739-751 |
artikel |
20 |
Colorectal Cancer Screening: Preferences, Past Behavior, and Future Intentions
|
Mansfield, Carol |
|
2018 |
|
6 |
p. 599-611 |
artikel |
21 |
Comment on Health Literacy: The Common Denominator of Healthcare Progress
|
Ibrahim, Halah |
|
|
|
6 |
p. 869-870 |
artikel |
22 |
Community-Based Participatory Research: Incorporating the Integral Voice of Community in Study Design
|
Pizarro, Desirree |
|
|
|
6 |
p. 661-663 |
artikel |
23 |
Concerns about the Responsiveness of Generic Measures and the Search for a “Minimally” Important Change: Today’s PRO Red Herrings
|
Cella, David |
|
|
|
6 |
p. 655-656 |
artikel |
24 |
Conducting Qualitative Research Online: Challenges and Solutions
|
Carter, Stacy M. |
|
|
|
6 |
p. 711-718 |
artikel |
25 |
Converting Parkinson-Specific Scores into Health State Utilities to Assess Cost-Utility Analysis
|
Chen, Gang |
|
2018 |
|
6 |
p. 665-675 |
artikel |
26 |
Designing HIV Testing and Self-Testing Services for Young People in Nigeria: A Discrete Choice Experiment
|
Ong, Jason J. |
|
|
|
6 |
p. 815-826 |
artikel |
27 |
Development and Acceptability of a Patient Decision Aid for Pain Management in Juvenile Idiopathic Arthritis: The JIA Option Map
|
Toupin-April, Karine |
|
|
|
6 |
p. 719-728 |
artikel |
28 |
Development and Validation of a Cross-Country Hospital Patient Quality of Care Assessment Tool in Europe
|
Villiers-Tuthill, Amanda |
|
2017 |
|
6 |
p. 753-761 |
artikel |
29 |
Development of a Discrete Choice Experiment (DCE) Questionnaire to Understand Veterans’ Preferences for Tobacco Treatment in Primary Care
|
Katz, David A. |
|
2018 |
|
6 |
p. 649-663 |
artikel |
30 |
Development of an Item Bank to Assess Patient-Reported Outcomes: Signs, Symptoms, and Impacts of COVID-19
|
Reaney, Matthew |
|
|
|
6 |
p. 703-713 |
artikel |
31 |
Discrete-Choice Experiment to Understand the Preferences of Patients with Hormone-Sensitive Prostate Cancer in the USA, Canada, and the UK
|
Gonzalez, Juan Marcos |
|
|
|
6 |
p. 607-623 |
artikel |
32 |
Does Device or Connection Type Affect Health Preferences in Online Surveys?
|
Hartman, John D. |
|
|
|
6 |
p. 639-650 |
artikel |
33 |
Does Patient Preference Measurement in Decision Aids Improve Decisional Conflict? A Randomized Trial in Men with Prostate Cancer
|
Shirk, Joseph D. |
|
2017 |
|
6 |
p. 785-798 |
artikel |
34 |
Don’t Forget the Caregivers! A Discrete Choice Experiment Examining Caregiver Views of Integrated Youth Services
|
Hawke, Lisa D. |
|
|
|
6 |
p. 791-802 |
artikel |
35 |
Effect of Treatment Preference in Randomized Controlled Trials: Systematic Review of the Literature and Meta-Analysis
|
Delevry, Dimittri |
|
|
|
6 |
p. 593-609 |
artikel |
36 |
Eliciting What Matters Most to People: The Whiteboard Initiative Proof of Concept
|
Kastner, Kathy |
|
|
|
6 |
p. 767-768 |
artikel |
37 |
Erratum to: Capturing Patient-Reported Outcome (PRO) Data Electronically: The Past, Present, and Promise of ePRO Measurement in Clinical Trials
|
Coons, Stephen Joel |
|
2015 |
|
6 |
p. 571 |
artikel |
38 |
Erratum to: Validity of a New Patient Engagement Measure: The Altarum Consumer Engagement (ACE) Measure™
|
Duke, Christopher C. |
|
2015 |
|
6 |
p. 569 |
artikel |
39 |
Ethics Review of Survey Research: A Mandatory Requirement for Publication?
|
Whicher, Danielle |
|
2015 |
|
6 |
p. 477-482 |
artikel |
40 |
Exploring the Impact of Infusion Frequency in Hemophilia A: Exit Interviews with Patients Participating in BAY 94-9027 Extension Studies (PROTECT VIII)
|
Wells, Jane R. |
|
|
|
6 |
p. 611-619 |
artikel |
41 |
Face Validity of Four Preference-Weighted Quality-of-Life Measures in Residential Aged Care: A Think-Aloud Study
|
Engel, Lidia |
|
|
|
6 |
p. 655-666 |
artikel |
42 |
Factors in Patient Empowerment: A Survey of an Online Patient Research Network
|
Chiauzzi, Emil |
|
2016 |
|
6 |
p. 511-523 |
artikel |
43 |
FDA Guidance on Assessment of Patient-Reported Outcomes in Cancer Trials: A Breath of Fresh Air or a Storm in a Teacup?
|
Gnanasakthy, Ari |
|
|
|
6 |
p. 695-697 |
artikel |
44 |
Gauging Incentive Values and Expectations (G.I.V.E.) among Blood Donors for Nonmonetary Incentives: Developing a Preference Elicitation Instrument through Qualitative Approaches in Shandong, China
|
Wang, Yu |
|
|
|
6 |
p. 593-606 |
artikel |
45 |
High Users of Healthcare Services: Development and Alpha Testing of a Patient Decision Aid for Case Management
|
Poitras, Marie-Eve |
|
|
|
6 |
p. 757-766 |
artikel |
46 |
How the 10th ISDM Conference Got to Qualify as “Patients Included™”: Insight from Inside
|
Ndiaye, Mame-Awa |
|
|
|
6 |
p. 645-648 |
artikel |
47 |
Identifying and Prioritizing the Barriers and Facilitators to the Self-Management of Type 2 Diabetes Mellitus: A Community-Centered Approach
|
Oakes, Allison H. |
|
2017 |
|
6 |
p. 773-783 |
artikel |
48 |
Impact of Elagolix on Workplace and Household Productivity Among Women with Moderate to Severe Pain Associated with Endometriosis: A Pooled Analysis of Two Phase III Trials
|
Surrey, Eric S. |
|
|
|
6 |
p. 651-660 |
artikel |
49 |
Increasing the Patient-Centeredness of Predictive Analytics Tools
|
Crossnohere, Norah L. |
|
|
|
6 |
p. 615-617 |
artikel |
50 |
Individual Preferences for Child and Adolescent Vaccine Attributes: A Systematic Review of the Stated Preference Literature
|
Michaels-Igbokwe, Christine |
|
2017 |
|
6 |
p. 687-700 |
artikel |
51 |
Individual Preferences for Child and Adolescent Vaccine Attributes: A Systematic Review of the Stated Preference Literature
|
Michaels-Igbokwe, Christine |
|
|
|
6 |
p. 687-700 |
artikel |
52 |
Information and Decision-Making Needs Among People with Anxiety Disorders: Results of an Online Survey
|
Liebherz, Sarah |
|
2015 |
|
6 |
p. 531-539 |
artikel |
53 |
Innovation in Chronic Kidney Disease: The Need for the Patient Voice
|
Fowler, Kevin |
|
2017 |
|
6 |
p. 673-676 |
artikel |
54 |
Interpreting Within-Patient Changes on the EORTC QLQ-C30 and EORTC QLQ-LC13
|
Coon, Cheryl D. |
|
|
|
6 |
p. 691-702 |
artikel |
55 |
Is Shared Decision Making a Utopian Dream or an Achievable Goal?
|
Blair, Louisa |
|
2015 |
|
6 |
p. 471-476 |
artikel |
56 |
It’s Time for Shared Decision Making and Person-Centred Care
|
Härter, Martin |
|
|
|
6 |
p. 643-644 |
artikel |
57 |
Maximum Acceptable Risk Estimation Based on a Discrete Choice Experiment and a Probabilistic Threshold Technique
|
Veldwijk, Jorien |
|
|
|
6 |
p. 641-653 |
artikel |
58 |
Meaningful Improvement in General Health Outcomes with Guselkumab Treatment for Psoriatic Arthritis: Patient-Reported Outcomes Measurement Information System-29 Results from a Phase 3 Study
|
Orbai, Ana-Maria |
|
|
|
6 |
p. 657-668 |
artikel |
59 |
Methods for Conducting Stated Preference Research with Children and Adolescents in Health: A Scoping Review of the Application of Discrete Choice Experiments
|
Michaels-Igbokwe, Christine |
|
|
|
6 |
p. 741-758 |
artikel |
60 |
Methods to Summarize Discrete-Choice Experiments in a Systematic Review: A Scoping Review
|
Choudhary, Daksh |
|
|
|
6 |
p. 629-639 |
artikel |
61 |
Oh, the Places We’ll Go: Patient-Reported Outcomes and Electronic Health Records
|
Gensheimer, Sarah G. |
|
2018 |
|
6 |
p. 591-598 |
artikel |
62 |
Operationalizing the Chronic Care Model with Goal-Oriented Care
|
Grudniewicz, Agnes |
|
|
|
6 |
p. 569-578 |
artikel |
63 |
Opportunities to Improve Long COVID Care: Implications from Semi-structured Interviews with Black Patients
|
Bergmans, Rachel S. |
|
|
|
6 |
p. 715-728 |
artikel |
64 |
Patient and Family Caregiver Considerations When Selecting Early Breast Cancer Treatment: Implications for Clinical Pathway Development
|
Schulman-Green, Dena |
|
|
|
6 |
p. 683-697 |
artikel |
65 |
Patient and Physician Perspectives on MSdialog, an Electronic PRO Diary in Multiple Sclerosis
|
Greiner, Peter |
|
2015 |
|
6 |
p. 541-550 |
artikel |
66 |
Patient and Public Preferences for Treatment Attributes in Parkinson’s Disease
|
Weernink, Marieke G. M. |
|
2017 |
|
6 |
p. 763-772 |
artikel |
67 |
Patient-Centered Core Impact Sets: What They are and Why We Need Them
|
Perfetto, Eleanor M. |
|
|
|
6 |
p. 619-627 |
artikel |
68 |
Patient-Consent Disconnects in Clinical Research
|
Dickert, Neal W. |
|
2018 |
|
6 |
p. 577-579 |
artikel |
69 |
Patient Engagement Partnerships in Clinical Trials: Development of Patient Partner and Investigator Decision Aids
|
Parry, Monica |
|
|
|
6 |
p. 745-756 |
artikel |
70 |
Patient Medication Preferences for Managing Dry Eye Disease: The Importance of Medication Side Effects
|
Ozdemir, Semra |
|
|
|
6 |
p. 679-690 |
artikel |
71 |
Patient-Oriented Research from the ISDM 2019 Conference: A Legacy Now More Relevant Than Ever
|
Archambault, Patrick M. |
|
|
|
6 |
p. 649-652 |
artikel |
72 |
Patient-Powered Research Networks of the Autoimmune Research Collaborative: Rationale, Capacity, and Future Directions
|
Nowell, W. Benjamin |
|
|
|
6 |
p. 699-710 |
artikel |
73 |
Patient Preferences for Breast Cancer Treatment Interventions: A Systematic Review of Discrete Choice Experiments
|
Guerra, Renata Leborato |
|
|
|
6 |
p. 559-569 |
artikel |
74 |
Patient Preferences in Diagnostic Imaging: A Scoping Review
|
Baird, Trey A. |
|
|
|
6 |
p. 579-591 |
artikel |
75 |
Patient-Reported Experience and Outcome Measures in People Living with Diabetes: A Scoping Review of Instruments
|
Martin-Delgado, Jimmy |
|
|
|
6 |
p. 759-773 |
artikel |
76 |
Patient-Reported Outcomes Through 1 Year of an HIV-1 Clinical Trial Evaluating Long-Acting Cabotegravir and Rilpivirine Administered Every 4 or 8 Weeks (ATLAS-2M)
|
Chounta, Vasiliki |
|
|
|
6 |
p. 849-862 |
artikel |
77 |
Patients’ Awareness, Usage and Impact of Hospital Report Cards in the US
|
Emmert, Martin |
|
2017 |
|
6 |
p. 729-738 |
artikel |
78 |
Patients’ Early Post-Operative Experiences with Lung Transplantation: A Longitudinal Qualitative Study
|
Seiler, Annina |
|
2016 |
|
6 |
p. 547-557 |
artikel |
79 |
Patients’ Lived Experiences of Nocturia: A Qualitative Study of the Evening, the Night, and the Next Day
|
Trigg, Andrew |
|
2017 |
|
6 |
p. 711-718 |
artikel |
80 |
Patients’ Preferences for Genomic Diagnostic Testing in Chronic Lymphocytic Leukaemia: A Discrete Choice Experiment
|
Buchanan, James |
|
2016 |
|
6 |
p. 525-536 |
artikel |
81 |
Preferences for Use and Design of Electronic Patient-Reported Outcomes in Patients with Chronic Obstructive Pulmonary Disease
|
Dumais, Kelly M. |
|
|
|
6 |
p. 621-629 |
artikel |
82 |
Putting Patients at the Centre of Healthcare: Progress and Challenges for Health Technology Assessments
|
Facey, Karen M. |
|
2018 |
|
6 |
p. 581-589 |
artikel |
83 |
Regulating Between the Notes: The US FDA and the Evolution of the Patient Voice Through Twenty-First Century Regulatory Science
|
Pitts, Peter J. |
|
|
|
6 |
p. 611-613 |
artikel |
84 |
Shared Decision Making in a Youth Mental Health Service Design and Research Project: Insights From the Pan-Canadian ACCESS Open Minds Network
|
Guinaudie, Chloé |
|
|
|
6 |
p. 653-666 |
artikel |
85 |
Shared Decision Making in Surgery: A Meta-Analysis of Existing Literature
|
Niburski, Kacper |
|
|
|
6 |
p. 667-681 |
artikel |
86 |
Spillover Effects of Maternal Chronic Disease on Children’s Quality of Life and Behaviors Among Low-Income Families
|
Guo, Vivian Y. W. |
|
2018 |
|
6 |
p. 625-635 |
artikel |
87 |
Systematic Review of Patients’ and Parents’ Preferences for ADHD Treatment Options and Processes of Care
|
Schatz, Nicole K. |
|
2015 |
|
6 |
p. 483-497 |
artikel |
88 |
Talking About Breast Cancer: Which Symptoms and Treatment Side Effects are Important to Patients with Advanced Disease?
|
Niklasson, Anna |
|
2017 |
|
6 |
p. 719-727 |
artikel |
89 |
The Health-Related Quality of Life of Chinese Patients on Hemodialysis and Peritoneal Dialysis
|
Chen, Julie Yun |
|
2017 |
|
6 |
p. 799-808 |
artikel |
90 |
The Impact of Chronic Urticaria from the Patient’s Perspective: A Survey in Five European Countries
|
Balp, Maria-Magdalena |
|
2015 |
|
6 |
p. 551-558 |
artikel |
91 |
The Impact of Patient Support Programs in Europe: A Systematic Literature Review
|
Sacristán, José Antonio |
|
|
|
6 |
p. 641-654 |
artikel |
92 |
The Impact of the Risk Functional Form Assumptions on Maximum Acceptable Risk Measures
|
Gonzalez, Juan Marcos |
|
|
|
6 |
p. 827-836 |
artikel |
93 |
The Perspectives of Patients with Chronic Diseases and Their Caregivers on Self-Management Interventions: A Scoping Review of Reviews
|
Niño de Guzmán Quispe, Ena |
|
|
|
6 |
p. 719-740 |
artikel |
94 |
The Predictive Value of Discrete Choice Experiments in Public Health: An Exploratory Application
|
Salampessy, Benjamin H. |
|
2015 |
|
6 |
p. 521-529 |
artikel |
95 |
13th Meeting of the International Academy of Health Preference Research
|
|
|
|
|
6 |
p. 729-738 |
artikel |
96 |
12th Meeting of the International Academy of Health Preference Research
|
|
|
|
|
6 |
p. 863-868 |
artikel |
97 |
Translating Evidence to Facilitate Shared Decision Making: Development and Usability of a Consult Decision Aid Prototype
|
Stacey, Dawn |
|
2016 |
|
6 |
p. 571-582 |
artikel |
98 |
Treatment Burden and Chronic Illness: Who is at Most Risk?
|
Sav, Adem |
|
2016 |
|
6 |
p. 559-569 |
artikel |
99 |
Unlocking the Value of Literature in Health Co-Design: Transforming Patient Experience Publications into a Creative and Accessible Card Tool
|
Villalba, Clare |
|
2018 |
|
6 |
p. 637-648 |
artikel |
100 |
Using Mind Mapping in Family Meetings to Support Shared Decision Making with Pediatric and Geriatric Patients
|
Russell, Matthew L. |
|
|
|
6 |
p. 709-717 |
artikel |
101 |
Using PROMs in Healthcare: Who Should Be in the Driving Seat—Policy Makers, Health Professionals, Methodologists or Patients?
|
Haywood, Kirstie L. |
|
2016 |
|
6 |
p. 495-498 |
artikel |
102 |
Validity of a New Patient Engagement Measure: The Altarum Consumer Engagement (ACE) Measure™
|
Duke, Christopher C. |
|
2015 |
|
6 |
p. 559-568 |
artikel |
103 |
Valuing End-of-Life Care for Older People with Advanced Cancer: Is Dying at Home Important?
|
Kenny, Patricia |
|
|
|
6 |
p. 803-813 |
artikel |
104 |
Views of the UK General Public on Important Aspects of Health Not Captured by EQ-5D
|
Shah, Koonal Kirit |
|
2017 |
|
6 |
p. 701-709 |
artikel |
105 |
What Do Users of Generic Medicines Think of Them? A Systematic Review of Consumers’ and Patients’ Perceptions of, and Experiences with, Generic Medicines
|
Dunne, Suzanne S. |
|
2016 |
|
6 |
p. 499-510 |
artikel |
106 |
What Matters for Evaluating the Quality of Mental Healthcare? Identifying Important Aspects in Qualitative Focus Groups with Service Users and Frontline Mental Health Professionals
|
Powell, Philip A. |
|
|
|
6 |
p. 669-678 |
artikel |
107 |
What Matters Most for Treatment Decisions in Hepatitis C: Effectiveness, Costs, and Altruism
|
Mattingly, T. Joseph |
|
|
|
6 |
p. 631-638 |
artikel |
108 |
What Matters Most for Treatment Decisions in Hepatitis C: Effectiveness, Costs, and Altruism
|
Mattingly, T. Joseph |
|
|
|
6 |
p. 631-638 |
artikel |
109 |
Women’s Preferences for Birthing Hospital in Denmark: A Discrete Choice Experiment
|
Tayyari Dehbarez, Nasrin |
|
2018 |
|
6 |
p. 613-624 |
artikel |