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Advising on Preferred Reporting Items for patient-reported outcome instrument development: the PRIPROID
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Advising on Preferred Reporting Items for patient-reported outcome instrument development: the PRIPROID (2012)Advising on Preferred Reporting Items for…Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement (2010)Preferred reporting items for…Guidance for Developers of Health Research Reporting Guidelines (2010)Guidance for Developers of He…CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Statement: updat…CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Statement: updat…Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement (2009)Preferred reporting items for…The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies (2008)The Strengthening the Reporti…Methods and Processes of the CONSORT Group: Example of an Extension for Trials Assessing Nonpharmacologic Treatments (2008)Methods and Processes of the …CONSORT for Reporting Randomized Controlled Trials in Journal and Conference Abstracts: Explanation and Elaboration (2008)CONSORT for Reporting Randomi…The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)The Strengthening the Reporti…The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies (2007)The Strengthening the Reporti…The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)The Strengthening the Reporti…Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance (2006)Guidance for industry: patien…Assessing Quality Of Life In Clinical Trials (2005)Assessing Quality Of Life In …Assessing health status and quality-of-life instruments: Attributes and review criteria (2002)Assessing health status and q…Research guidelines for the Delphi survey technique (2000)Research guidelines for the D…Recommendations on health-related quality of life research to support labeling and promotional claims in the United States (2000)Recommendations on health-rel…Cochrane Handbook for Systematic Reviews of Interventions (2008)The PRISMA Statement for Reporting Systematic Reviews and Meta-Analyses of Studies That Evaluate Health Care Interventions: Explanation and Elaboration (2009)The PRISMA 2020 statement: an updated guideline for reporting systematic reviews (2021)The PRISMA 2020 statement: an updated guideline for reporting systematic reviews (2021)The PRISMA 2020 statement: An updated guideline for reporting systematic reviews (2021)Improving the quality of reports of meta-analyses of randomised controlled trials: the QUOROM statement (1999)The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials (2001)Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration (2007)CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (2010)Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide (2014)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. 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(2020)Prevalence of mental health problems during the COVID-19 pandemic: A systematic review and meta-analysis (2020)SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials (2013)Transparent Reporting of a multivariable prediction model for Individual Prognosis Or Diagnosis (TRIPOD): Explanation and Elaboration (2015)Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups (2007)Development and Validation of Patient-Reported Outcome Measures for Sleep Disturbance and Sleep-Related Impairments (2010)The COSMIN checklist for assessing the methodological quality of studies on measurement properties of health status measurement instruments: an international Delphi study (2010)Measuring financial toxicity as a clinically relevant patient‐reported outcome: The validation of the COmprehensive Score for financial Toxicity (COST) (2016)Transparent reporting of a multivariable prediction model for individual prognosis or diagnosis (TRIPOD): the TRIPOD statement (2015)Assessing the quality of studies in meta-analyses: Advantages and limitations of the Newcastle Ottawa Scale (2017)Physical, psychological and occupational consequences of job burnout: A systematic review of prospective studies (2017)
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References

  • 2009Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement83,813 cited
  • 2007The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies22,917 cited
  • 2007The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies21,132 cited
  • 2007The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies17,756 cited
  • 2008The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies17,743 cited
  • 2010CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials13,365 cited
  • 2010Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement12,147 cited
  • 2010CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials9,314 cited
  • 2000Research guidelines for the Delphi survey technique5,943 cited
  • 2006Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance2,855 cited
  • 2002Assessing health status and quality-of-life instruments: Attributes and review criteria2,267 cited
  • 2010Guidance for Developers of Health Research Reporting Guidelines1,432 cited
  • 2008

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CONSORT for Reporting Randomized Controlled Trials in Journal and Conference Abstracts: Explanation and Elaboration
670 cited
  • 2000Recommendations on health-related quality of life research to support labeling and promotional claims in the United States577 cited
  • 2008Methods and Processes of the CONSORT Group: Example of an Extension for Trials Assessing Nonpharmacologic Treatments522 cited
  • 2005Assessing Quality Of Life In Clinical Trials261 cited
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