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Journal of Patient-Reported Outcomes
Titel
Veröffentlichungsdatum
Sprache
Zitate
An emerging framework for fully incorporating public involvement (PI) into patient-reported outcome measures (PROMs)
2020/01/13
English
29
Selecting, implementing and evaluating patient-reported outcome measures for routine clinical use in cancer: the Cancer Care Ontario approach
2020/11/26
English
29
PRO-based follow-up as a means of self-management support – an interpretive description of the patient perspective
2018/09/05
English
28
Development and validation of the Ulcerative Colitis patient-reported outcomes signs and symptoms (UC-pro/SS) diary
2018/05/30
English
28
Good practices for the translation, cultural adaptation, and linguistic validation of clinician-reported outcome, observer-reported outcome, and performance outcome measures
2020/11/04
English
28
The responsiveness of the PROMIS instruments and the qDASH in an upper extremity population
2017/11/28
English
28
A comparison of three methods to generate a conceptual understanding of a disease based on the patients’ perspective
2017/12/01
English
27
The feasibility of implementing the ICHOM Standard Set for Hip and Knee Osteoarthritis: a mixed-methods evaluation in public and private hospital settings
2018/08/01
English
27
What is an estimand & how does it relate to quantifying the effect of treatment on patient-reported quality of life outcomes in clinical trials?
2020/08/24
English
26
EQ-5D: a plea for accurate nomenclature
2020/07/03
English
25
Patient-reported outcome measures in the interaction between patient and clinician – a multi-perspective qualitative study
2020/01/09
English
25
Japanese translation and linguistic validation of the US National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
2017/12/01
English
25
The development of PROmunication: a training-tool for clinicians using patient-reported outcomes to promote patient-centred communication in clinical cancer settings
2020/02/11
English
24
Core outcome sets in cancer and their approaches to identifying and selecting patient-reported outcome measures: a systematic review
2020/09/15
English
24
Selection of patient-reported outcome measures (PROMs) for use in health systems
2021/10/01
English
23
Patient experience after kidney transplant: a conceptual framework of treatment burden
2019/01/30
English
23
Exploring the quality of life issues in people with retinal diseases: a qualitative study
2017/09/21
English
23
Incorporating patient experience into drug development for ulcerative colitis: development of the Urgency Numeric Rating Scale, a patient-reported outcome measure to assess bowel urgency in adults
2022/04/01
English
23
Personalized symptom management: a quality improvement collaborative for implementation of patient reported outcomes (PROs) in ‘real-world’ oncology multisite practices
2020/06/17
English
22
A multicenter paper-based and web-based system for collecting patient-reported outcome measures in patients undergoing local treatment for prostate cancer: first experiences
2020/07/13
English
22
A systematic evaluation of compliance and reporting of patient-reported outcome endpoints in ovarian cancer randomised controlled trials: implications for generalisability and clinical practice
2017/10/04
English
22
The Japanese version of the National Cancer Institute’s patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE): psychometric validation and discordance between clinician and patient assessments of adverse events
2018/01/05
English
22
Collection and use of EQ-5D for follow-up, decision-making, and quality improvement in health care - the case of the Swedish National Quality Registries
2020/09/16
English
22
Mental health impact on healthcare workers due to the COVID-19 pandemic: a U.S. cross-sectional survey study
2022/06/13
English
21
Psychometric validation of the work productivity and activity impairment questionnaire in ulcerative colitis: results from a systematic literature review
2018/12/01
English
21
Development and content validation of two new patient-reported outcome measures for endometriosis: the Endometriosis Symptom Diary (ESD) and Endometriosis Impact Scale (EIS)
2020/02/18
English
20
Facilitators and barriers to implementing electronic patient-reported outcome and experience measures in a health care setting: a systematic review
2023/02/14
English
20
Psychometric evaluation of the PROMIS® Depression Item Bank: an illustration of classical test theory methods
2019/07/30
English
20
The impact of patient-reported outcome data from clinical trials: perspectives from international stakeholders
2020/07/02
English
20
Patient experiences with hypertrophic cardiomyopathy: a conceptual model of symptoms and impacts on quality of life
2020/12/01
English
19
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