Patient involvement in the development of patient‐reported outcome measures
A scoping review
Bibliographic Data
| ID | 19509080 |
|---|---|
| Authors | Bianca Wiering (0000-0001-6708-5705, Tranzo (Scientific Centre for Transformation in Care and Welfare) Tilburg University Tilburg The Netherlands, corresponding author), Dolf de Boer (0000-0002-3812-5402, Nivel (Netherlands Institute for Health Services Research) Utrecht The Netherlands), Diana Delnoij (0000-0002-2066-9604, Tranzo (Scientific Centre for Transformation in Care and Welfare) Tilburg University Tilburg The Netherlands) |
| Year | 2017 |
| Volume | 20 |
| Issue | 1 |
| Pages | 11-23 |
| Publication date | 2017-02-01 |
| Peer Reviewed | Yes |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Health Expectations (JOURNAL) |
| Journal identifiers | ISSN: 1369-6513 • E-ISSN: 1369-7625 |
| Publisher | Wiley (PUBLISHER • GB) |
| DOI | 10.1111/hex.12442 |
| PMID | 26889874 |
| OpenAlex | W2280696905 |
| Language | EN |
| Citations received | 31 |
| References cited | 46 |
Family medicine · Health care · MEDLINE · Patient-reported outcome · Prom · Cancer survivorship and care · Medicine · Mental Health and Patient Involvement · Nursing · Patient-Provider Communication in Healthcare
Purpose, Functionality and Reconceptualisation of Patient-Reported Outcome
What are the Key Characteristics of a ‘Good’ Psychotherapy? Calling for Ethical Patient Involvement
Validity and Reliability of the Transcultural Arabic Adaptation of the Food-Mood Questionnaire Among College Students
Further Development and Validation of a Measure of Compassionate Healthcare in Action
Value redefined for inflammatory bowel disease patients
A philosophical perspective on the development and application of patient-reported outcomes measures (PROMs)
Exploration des challenges éthiques en pratique médicale quotidienne
A randomised online experimental study to compare responses to brief and extended surveys of health-related quality of life and psychosocial outcomes among women with breast cancer
Adaptation and content validation of measure yourself medical outcomes profile (Mymop) for 7–11 year-old children
Patient-centered outcomes on quality of life and anthroposophic healthcare
Patients’ and parents’ perspective on the implementation of Patient Reported Outcome Measures in pediatric clinical practice using the KLIK PROM portal
The importance of content and face validity in instrument development
Health-related quality of life in elderly, multimorbid individuals with and without depression and/or mild cognitive impairment using a telemonitoring application
Quality in Psychiatric Care in the Community Mental Health Setting from the Perspective of Patients and Staff
Cross-State Validation of a Tool Supporting Implementation of Rural Kinship Navigator Programs
A Systematic Review Evaluating Psychometric Properties of Parent or Caregiver Report Instruments on Child Maltreatment
What matters to people with memory problems, healthy volunteers and health and social care professionals in the context of developing treatment to prevent Alzheimer's dementia? A qualitative study
Evaluating the Involvement of People With Cancer and Informal Caregivers in the Development Process of a New Set of Quality of Life Questionnaires
Asking what matters
Patient involvement in research – participants or collaborators
A codevelopment process to advance methods for the use of patient‐reported outcome measures and patient‐reported experience measures with people who are homeless and experience chronic illness
‘If we would change things outside we wouldn’t even need to go in…’ supporting recovery via community‐based actions
Implementation of a patient‐reported experience measure in a Dutch disability care organization
Development of an inflammatory bowel disease (IBD) Patient‐Reported Experience Measure (PREM)
Patient involvement vs. patient participation in qualitative research in the development of PROM s
Reconciling validity and challenges of patient comfort and understanding
Stakeholder engagement from problem analysis to implementation strategies for a patient‐reported experience measure in disability care
Public involvement in chronic respiratory diseases research
Involvement of people who use alcohol and other drug services in the development of patient‐reported measures of experience
The involvement of people living with HIV in the development of HIV-specific or inclusive health instruments
Questions regarding 'epistemic injustice' in knowledge-intensive policymaking
Health Measurement Scales
Content Validity—Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation
Content Validity—Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation
Evaluating patient-based outcome measures for use in clinical trials.
The PRISMA Statement for Reporting Systematic Reviews and Meta-Analyses of Studies That Evaluate Health Care Interventions
Patient reported outcome measures could help transform healthcare
Seeking the Patient's Perspective
The Cosmin checklist for assessing the methodological quality of studies on measurement properties of health status measurement instruments
Generic and Disease-Specific Measures in Assessing Health Status and Quality of Life
Scoping studies
| Unique citing works | 31 |
|---|---|
| Citations per year | 3,1 |
| Citation span | 2016 - 2026 (11) |
| Citation velocity | current |
| Highly cited | No |
| Citation types | Neutral: 27 |