SZodixStudyAcademic Library
ShelvesOpen access
Study · an open academic library·Metadata from OpenAlex (CC0)·Shelves·OpenAlex metadata, de-duplicated
SPIRIT 2025 explanation and elaboration: updated guideline for protocols of randomised trials
16 references·8 citing·34 second hop
SPIRIT 2025 explanation and elaboration: updated guideline for protocols of randomised trials (2025)SPIRIT 2025 explanation and elaboration: …RoB 2: a revised tool for assessing risk of bias in randomised trials (2019)RoB 2: a revised tool for ass…CONSORT Statement for Randomized Trials of Nonpharmacologic Treatments: A 2017 Update and a CONSORT Extension for Nonpharmacologic Trial Abstracts (2017)CONSORT Statement for Randomi…A manifesto for reproducible science (2017)A manifesto for reproducible …CONSORT 2010 statement: extension to randomised pilot and feasibility trials (2016)CONSORT 2010 statement: exten…Preferred Reporting Items for a Systematic Review and Meta-analysis of Individual Participant Data (2015)Preferred Reporting Items for…Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide (2014)Better reporting of intervent…SPIRIT 2013 Statement: Defining Standard Protocol Items for Clinical Trials (2013)SPIRIT 2013 Statement: Defini…SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials (2013)SPIRIT 2013 explanation and e…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 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Explanation and …Avoidable waste in the production and reporting of research evidence (2009)Avoidable waste in the produc…Extending the CONSORT Statement to Randomized Trials of Nonpharmacologic Treatment: Explanation and Elaboration (2008)Extending the CONSORT Stateme…Empirical Evidence for Selective Reporting of Outcomes in Randomized Trials (2004)Empirical Evidence for Select…Assessing the quality of controlled clinical trials (2001)Assessing the quality of cont…Empirical Evidence of Bias (1995)Empirical Evidence of BiasTIPS (Trans-Tasman Internet-delivered Prevention of (youth) Suicide) study: protocol for a randomised controlled trial of mobile health interventions (four apps) to help young people reduce suicidal ideation (2026)TIPS (Trans-Tasman Internet-d…The Preliminary Efficacy and Feasibility of SMILE Serious Game for Adolescents and Young Adults: Protocol for Cluster Randomized Multisite Adaptive Trial Design (2026)The Preliminary Efficacy and …Efficacy of a video‐viewing intervention of smartphone‐based positive word stimulation on depressive symptoms in individuals with subthreshold depression: Protocol for a randomized controlled trial (2026)Efficacy of a video‐viewing i…SPIRIT 2025 statement: updated guideline for protocols of randomized trials (2025)SPIRIT 2025 statement: update…SPIRIT 2025 statement: Updated guideline for protocols of randomised trials (2025)SPIRIT 2025 statement: Update…SPIRIT 2025 statement: updated guideline for protocols of randomised trials (2025)SPIRIT 2025 statement: update…SPIRIT 2025 Statement (2025)SPIRIT 2025 StatementDigital positive affect intervention (PAI) versus self-monitoring placebo in the treatment of anxiety and depression: a two-arm randomized controlled trial (RCT) (2025)Digital positive affect inter…The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment effects in controlled trials (1995)Does quality of reports of randomised trials affect estimates of intervention efficacy reported in meta-analyses? (1998)The CONSORT Statement: Revised Recommendations for Improving the Quality of Reports of Parallel-Group Randomized Trials (2001)The development of QUADAS: a tool for the quality assessment of studies of diagnostic accuracy included in systematic reviews (2003)Methods for the thematic synthesis of qualitative research in systematic reviews (2008)The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration (2009)CONSORT 2010 Statement: Updated Guidelines for Reporting Parallel Group Randomized Trials (2010)Reporting of Patient-Reported Outcomes in Randomized Trials (2013)Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement (2015)The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration (2009)The PRISMA Statement for Reporting Systematic Reviews and Meta-Analyses of Studies That Evaluate Health Care Interventions: Explanation and Elaboration (2009)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. (2009)Transparent Reporting of a multivariable prediction model for Individual Prognosis Or Diagnosis (TRIPOD): Explanation and Elaboration (2015)Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation (2015)Bioconda: sustainable and comprehensive software distribution for the life sciences (2018)The preregistration revolution (2018)Sustainable data analysis with Snakemake (2021)The Measurement of Observer Agreement for Categorical Data (1977)QUADAS-2: A Revised Tool for the Quality Assessment of Diagnostic Accuracy Studies (2011)The Cochrane Collaboration's tool for assessing risk of bias in randomised trials (2011)ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions (2016)The PRISMA 2020 statement: an updated guideline for reporting systematic reviews (2021)The PRISMA 2020 statement: an updated guideline for reporting systematic reviews (2021)Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups (2007)Guidelines for reporting non-randomised pilot and feasibility studies (2019)Two new Later Stone Age sites from the Final Pleistocene in the Falémé Valley, eastern Senegal (2024)CONSORT 2025 statement: updated guideline for reporting randomised trials (2025)CONSORT 2025 statement: updated guideline for reporting randomised trials (2025)CONSORT 2010 statement: extension to randomised pilot and feasibility trials (2016)CARE guidelines for case reports: explanation and elaboration document (2017)Assessing the quality of reports of randomized clinical trials: Is blinding necessary? (1996)
this work references cited by second hop

References

  • 2019RoB 2: a revised tool for assessing risk of bias in randomised trials33,067 cited
  • 2014Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide10,521 cited
  • 2010CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials9,314 cited
  • 2010CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials8,873 cited
  • 2013SPIRIT 2013 Statement: Defining Standard Protocol Items for Clinical Trials7,356 cited
  • 2013SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials6,239 cited
  • 1995Empirical Evidence of Bias5,632 cited
  • 2016CONSORT 2010 statement: extension to randomised pilot and feasibility trials3,394 cited
  • 2017A manifesto for reproducible science3,368 cited
  • 2001Assessing the quality of controlled clinical trials3,309 cited
  • 2008Extending the CONSORT Statement to Randomized Trials of Nonpharmacologic Treatment: Explanation and Elaboration2,290 cited
  • 2009Avoidable waste in the production and reporting of research evidence2,204 cited
  • 2015Preferred Reporting Items for a Systematic Review and Meta-analysis of Individual Participant Data2,123 cited
  • 2004Empirical Evidence for Selective Reporting of Outcomes in Randomized Trials

Only edges whose both ends are imported exist here. Widen the year window, or show the whole map. Back to the work

1,845 cited
  • 2017CONSORT Statement for Randomized Trials of Nonpharmacologic Treatments: A 2017 Update and a CONSORT Extension for Nonpharmacologic Trial Abstracts1,531 cited
  • 2010Guidance for Developers of Health Research Reporting Guidelines1,432 cited
  • Cited by

    • 2025SPIRIT 2025 statement: updated guideline for protocols of randomized trials134 cited
    • 2025SPIRIT 2025 statement: updated guideline for protocols of randomised trials107 cited
    • 2025SPIRIT 2025 Statement100 cited
    • 2025SPIRIT 2025 statement: Updated guideline for protocols of randomised trials68 cited
    • 2026TIPS (Trans-Tasman Internet-delivered Prevention of (youth) Suicide) study: protocol for a randomised controlled trial of mobile health interventions (four apps) to help young people reduce suicidal ideation1 cited
    • 2026Efficacy of a video‐viewing intervention of smartphone‐based positive word stimulation on depressive symptoms in individuals with subthreshold depression: Protocol for a randomized controlled trial1 cited
    • 2026The Preliminary Efficacy and Feasibility of SMILE Serious Game for Adolescents and Young Adults: Protocol for Cluster Randomized Multisite Adaptive Trial Design1 cited
    • 2025Digital positive affect intervention (PAI) versus self-monitoring placebo in the treatment of anxiety and depression: a two-arm randomized controlled trial (RCT)1 cited