| 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
|
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