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Journal of Patient-Reported Outcomes : Impact Factor & More

eISSN: 2509-8020pISSN: 2509-8020
JournalOpen Access

Aims and Scope of Journal of Patient-Reported Outcomes

The Journal of Patient-Reported Outcomes (JPRO) is an international, open access, multi-disciplinary journal publishing original manuscripts in the field of patient-reported outcomes (PRO). JPRO will consider original research and review articles, brief communications, commentaries, editorials, and reviews of recent books and software advances relevant to the following topics: PROs in clinical trials. PROs in clinical practice. Patient, family, community, and public engagement. Qualitative studies on the development and application of PROs. Studies of the social and behavioural determinants of health using PRO measures. Patient-Reported Experience Measures. Less

Key Metrics

CiteScore
3
SJR
Q3Health Informatics
SNIP
1
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Topics Covered on Journal of Patient-Reported Outcomes

Journal of Patient-Reported Outcomes Journal Specifications

Indexed in the following public directories

  • Web of Science Web of Science
  • Scopus Scopus
  • DOAJ DOAJ
  • SJR SJR
Overview
Publisher Springer Nature
Language English
Frequency Continuous publication
Article Processing ChargesGBP 960 | USD 1790
Publication Time20
Editorial Review ProcessDouble blind peer review
General Details
LanguageEnglish
Society/Institute/SponsorInternational Society for Quality of Life Research
FrequencyContinuous publication
Publisher URLVisit website
Website URLVisit website
Publication Details
PlagiarismVisit website
Publication Time 20
Waiver PolicyVisit website
Editorial Review Detail
Editorial TeamVisit website
Review ProcessDouble blind peer review
Review UrlVisit website
Information for authors
Author instructionsVisit website
Copyright DetailsVisit website
Deposit PolicySherpa/Romeo
License typeCC BY
OA statementVisit website
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Recently Published Papers in Journal of Patient-Reported Outcomes

Translation, adaptation and validation of Parkinson’s disease quality of life − 39 questionnaire to Yoruba language
  • 25 Jul 2026
  • Journal of Patient-Reported Outcomes
Higher severity of infant RSV infections is associated with lower parental quality of life \u2013 a European observational study
  • 24 Jul 2026
  • Journal of Patient-Reported Outcomes
Impact of translation availability on the patient voice in clinical trials: commentary.
  • 21 Jul 2026
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Using electronic patient reported outcomes (ePROs) to improve supportive care in ambulatory oncology care: a CFIR-guided pre-implementation formative evaluation.
  • 21 Jul 2026
  • Journal of patient-reported outcomes
Measuring fatigue four years after stroke: a bi-factor analysis of the Norwegian Chalder Fatigue Questionnaire.
  • 21 Jul 2026
  • Journal of patient-reported outcomes
Identifying patient profiles to personalize care and improve quality of life in EGPA patients: a national cross-sectional survey.
  • 20 Jul 2026
  • Journal of patient-reported outcomes
Translation, adaptation and validation of Parkinson’s disease quality of life − 39 questionnaire to Yoruba language
  • 25 Jul 2026
  • Journal of Patient-Reported Outcomes
Higher severity of infant RSV infections is associated with lower parental quality of life \u2013 a European observational study
  • 24 Jul 2026
  • Journal of Patient-Reported Outcomes
Impact of translation availability on the patient voice in clinical trials: commentary.
  • 21 Jul 2026
  • Journal of patient-reported outcomes
Using electronic patient reported outcomes (ePROs) to improve supportive care in ambulatory oncology care: a CFIR-guided pre-implementation formative evaluation.
  • 21 Jul 2026
  • Journal of patient-reported outcomes
Measuring fatigue four years after stroke: a bi-factor analysis of the Norwegian Chalder Fatigue Questionnaire.
  • 21 Jul 2026
  • Journal of patient-reported outcomes
Identifying patient profiles to personalize care and improve quality of life in EGPA patients: a national cross-sectional survey.
  • 20 Jul 2026
  • Journal of patient-reported outcomes

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