SZodixStudyAcademic Library
ShelvesOpen access
Study · an open academic library·Metadata from OpenAlex (CC0)·Shelves·OpenAlex metadata, de-duplicated
Descriptions of non-pharmacological interventions in clinical trials
7 references·4 citing·40 second hop
Descriptions of non-pharmacological interventions in clinical trials (2013)Descriptions of non-pharmacological inter…SPIRIT 2013 Statement: Defining Standard Protocol Items for Clinical Trials (2013)SPIRIT 2013 Statement: Defini…Poor description of non-pharmacological interventions: analysis of consecutive sample of randomised trials (2013)Poor description of non-pharm…The quality of reports of randomised trials in 2000 and 2006: comparative study of articles indexed in PubMed (2010)The quality of reports of ran…Avoidable waste in the production and reporting of research evidence (2009)Avoidable waste in the produc…What is missing from descriptions of treatment in trials and reviews? (2008)What is missing from descript…Extending the CONSORT Statement to Randomized Trials of Nonpharmacologic Treatment: Explanation and Elaboration (2008)Extending the CONSORT Stateme…The CONSORT statement: revised recommendations for improving the quality of reports of parallel group randomized trials (2001)The CONSORT statement: revise…Avoidable waste related to inadequate methods and incomplete reporting of interventions: a systematic review of randomized trials performed in Sub-Saharan Africa (2017)Avoidable waste related to in…Has the quality of reporting in periodontology changed in 14 years? A systematic review (2016)Has the quality of reporting …How well do randomised controlled trials of physical interventions for people with spinal cord injury adhere to the CONSORT guidelines? An analysis of trials published over a 10-year period (2014)How well do randomised contro…Providing adequate and practical descriptions in surgical trials (2013)Providing adequate and practi…Health Measurement Scales: A Practical Guide to Their Development and Use (1989)Assessing the quality of reports of randomized clinical trials: Is blinding necessary? (1996)Meta-analysis of Observational Studies in Epidemiology A Proposal for Reporting (2000)Core outcome domains for chronic pain clinical trials: IMMPACT recommendations (2003)Improving the Reporting Quality of Nonrandomized Evaluations of Behavioral and Public Health Interventions: The TREND Statement (2004)Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration (2007)Improving the quality of reporting of randomized controlled trials. The CONSORT statement (1996)Assessing the quality of controlled clinical trials (2001)The Revised CONSORT Statement for Reporting Randomized Trials: Explanation and Elaboration (2001)CONSORT 2010 Statement (2010)CONSORT 2010 Statement: updated guidelines for reporting parallel group randomized trials. (2010)Effect of Preventive Interventions in Mentally Ill Parents on the Mental Health of the Offspring: Systematic Review and Meta-Analysis (2011)Improving the quality of reports of meta-analyses of randomised controlled trials: the QUOROM statement (1999)Empirical Evidence for Selective Reporting of Outcomes in Randomized Trials (2004)Avoidable Waste in the Production and Reporting of Research Evidence (2009)A refined taxonomy of behaviour change techniques to help people change their physical activity and healthy eating behaviours: The CALO-RE taxonomy (2011)Behaviour change techniques: the development and evaluation of a taxonomic method for reporting and describing behaviour change interventions (a suite of five studies involving consensus methods, randomised controlled trials and analysis of qualitative data) (2015)SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials (2013)Consensus on Exercise Reporting Template (CERT): Modified Delphi Study (2016)Enhancing the usability of systematic reviews by improving the consideration and description of interventions (2017)CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials (2025)Empirical Evidence of Bias (1995)Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration (2007)The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)The Behavior Change Technique Taxonomy (v1) of 93 Hierarchically Clustered Techniques: Building an International Consensus for the Reporting of Behavior Change Interventions (2013)CONSORT 2010 statement: extension to randomised pilot and feasibility trials (2016)CONSORT 2010 statement: extension to randomised pilot and feasibility trials (2016)CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)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 Measurement of Observer Agreement for Categorical Data (1977)Quality assessment of randomized controlled trial abstracts on drug therapy of periodontal disease from the abstracts published in dental Science Citation Indexed journals in the last ten years (2020)Study design and primary outcome in randomized controlled trials in periodontology. A systematic review (2021)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement (2009)Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement (2009)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. (2009)Reducing waste from incomplete or unusable reports of biomedical research (2014)CONSORT Statement for Randomized Trials of Nonpharmacologic Treatments: A 2017 Update and a CONSORT Extension for Nonpharmacologic Trial Abstracts (2017)The COMET Handbook: version 1.0 (2017)
this work references cited by second hop

References

  • 2013SPIRIT 2013 Statement: Defining Standard Protocol Items for Clinical Trials7,356 cited
  • 2001The CONSORT statement: revised recommendations for improving the quality of reports of parallel group randomized trials2,754 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
  • 2008What is missing from descriptions of treatment in trials and reviews?613 cited
  • 2010The quality of reports of randomised trials in 2000 and 2006: comparative study of articles indexed in PubMed503 cited
  • 2013Poor description of non-pharmacological interventions: analysis of consecutive sample of randomised trials374 cited

Cited by

  • 2017Avoidable waste related to inadequate methods and incomplete reporting of interventions: a systematic review of randomized trials performed in Sub-Saharan Africa13 cited
  • 2016Has the quality of reporting in periodontology changed in 14 years? A systematic review12 cited
  • 2013Providing adequate and practical descriptions in surgical trials11 cited
  • 2014How well do randomised controlled trials of physical interventions for people with spinal cord injury adhere to the CONSORT guidelines? An analysis of trials published over a 10-year period9 cited

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