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Importance of peer review – request for reviewers
The Editors of Journal of Patient Reported Outcomes would like to encourage readers to sign up to become reviewers for the journal.
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2023 ISOQOL Annual Conference
30 Years of ISOQOL: Quality of Life - making it relevant
18-21 October 2023 - Calgary, Alberta, Canada
Over the past 30 years, ISOQOL has made an important impact internationally on the use of PROs in both commercial and academic research. In addition to expanding on this legacy, this year’s conference will focus on identifying the many barriers that limit the use of PROs in day to day patient care and formulate practical solutions to overcome those barriers.
Important Dates
- 23 January 2023: Workshop and Symposium Abstract Submissions Due
- 3 April 2023: Oral, Brief & Poster Presentation Abstract Submissions Due
- 1 May 2023: Scholarship Applications Due
2023 ISOQOL MWM Symposium
Measuring What Matters in Oncology: Translating research into clinical practice using clinical quality registries
Cancers are a leading cause of morbidity and mortality globally. Clinical quality registries (CQRs) are recognized as important tools for monitoring and evaluating quality of care in such diseases by measuring variation from what is considered evidence-based, optimal practice (defined a priori by a consensus process involving clinical experts and consumers). The complementary use of clinical and patient-reported data provide comprehensive assessment of the impact of compliance and through insights into variations between institutions (through benchmarking performance) CQRs provide invaluable opportunities for implementation research.
For more information about the symposium visit: https://www.pathlms.com/isoqol/webinars/32102
Peer review
Journal of Patient-Reported Outcomes operates a double-blind peer-review system and further details are available in our peer review policy. If you are new to peer review, you can read an overview of the peer review process and its benefits. Also, please see resources for reviewers, including training and tutorials, and information about receiving recognition for your involvement.
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Measuring symptom burden in patients with cancer during a pandemic: the MD Anderson symptom inventory for COVID-19 (MDASI-COVID)
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Structural equation model of coping and life satisfaction of community-dwelling older people during the COVID-19 pandemic
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Psychometric evaluation of the Symptoms of Infection with Coronavirus-19 (SIC): results from a cross-sectional study and a phase 3 clinical trial
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Feasibility of PROMIS using computerized adaptive testing during inpatient rehabilitation
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Towards the use of mixed methods inquiry as best practice in health outcomes research
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What is an estimand & how does it relate to quantifying the effect of treatment on patient-reported quality of life outcomes in clinical trials?
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Describing the emotional exhaustion, depersonalization, and low personal accomplishment symptoms associated with Maslach Burnout Inventory subscale scores in US physicians: an item response theory analysis
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How do patient reported outcome measures (PROMs) support clinician-patient communication and patient care? A realist synthesis
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Measurement of alienation among adolescents: construct validity of three scales on powerlessness, meaninglessness and social isolation
Editors-in-Chief
Chih-Hung Chang , Editor-in-Chief
Washington University in St. Louis, USA
Rasa Ruseckaite , Editor-in-Chief
Monash University in Melbourne, Australia
Indexing
We are pleased to announce that all articles published in Journal of Patient-Reported Outcomes are included in the Emerging Sources Citation Index, Web of Science, Scopus, PubMed, PubMed Central and DOAJ.
Aims and scope
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.
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Promoting your article
Once your paper is accepted and published in Journal of Patient-Reported Outcomes, increase your reach by tweeting the link to your published paper and tagging @ISOQOL and/or @JPRO_ISOQOL
About the Society
The International Society for Quality of Life Research (ISOQOL) is a global community of researchers, clinicians, health care professionals, industry professionals, consultants, and patient research partners advancing health related quality of life research (HRQL).
Together, we are creating a future in which patient perspective is integral to health research, care and policy.
- ISSN: 2509-8020 (electronic)
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Annual Journal Metrics
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Citation Impact
1.145 - Source Normalized Impact per Paper (SNIP)
0.803 - SCImago Journal Rank (SJR)
2.000 - CiteScoreSpeed
49 days to first decision for all manuscripts (Median)
55 days to first decision for reviewed manuscripts only (Median)Usage
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