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SPIRIT-Children and Adolescents

Transparent reporting of observational studies emulating a target trial: the TARGET Statement

Reporting guidelines for tear fluid research

Development of GROVE: A Guideline for RepOrting Vignette Experiments conducted in a healthcare context

Reporting of cluster randomised crossover trials: extension of the CONSORT 2010 statement with explanation and elaboration

Developing the TIDieR-Rehab checklist: a modified Delphi process to extend the Template for Intervention Description and Replication (TIDieR) for rehabilitation intervention reporting

Reporting guidelines for randomised controlled trial reports of implantable neurostimulation devices: the CONSORT-iNeurostim extension

Reporting guidelines for protocols of randomised controlled trials of implantable neurostimulation devices: the SPIRIT-iNeurostim extension

Reflexology specific guidance for using the template for the intervention description and replication (TIDieR): A delphi study

Moving Forward on Tumor Pathology Research Reporting: A Guide for Pathologists From the World Health Organization Classification of Tumors Living Evidence Gap Map by Tumour Type Group

Guideline for RSA and CT-RSA implant migration measurements: an update of standardizations and recommendations

Publication guidelines for human heart rate and heart rate variability studies in psychophysiology-Part 1: Physiological underpinnings and foundations of measurement

Standardized reporting on studies of psychiatric pharmacist interventions

Enhancing the quality of evidence, comparability, and reproducibility in ventriculoatrial shunt research for normal pressure hydrocephalus: A systematic review and VAS-NPH reporting guideline

The OHStat Guidelines for Reporting Observational Studies and Clinical Trials in Oral Health Research: Manuscript Checklist

Reporting of surrogate endpoints in randomised controlled trial reports (CONSORT-Surrogate): extension checklist with explanation and elaboration

Reporting of surrogate endpoints in randomised controlled trial protocols (SPIRIT-Surrogate): extension checklist with explanation and elaboration

Biofield therapies: Guidelines for reporting clinical trials

REPORT-SCS: minimum reporting standards for spinal cord stimulation studies in spinal cord injury

Trial Forge Guidance 4: a guideline for reporting the results of randomised Studies Within A Trial (SWATs)

We don’t know what you did last summer. On the importance of transparent reporting of reaction time data pre-processing

The SHARE: SHam Acupuncture REporting guidelines and a checklist in clinical trials

Development of the Reporting Infographics and Visual Abstracts of Comparative studies (RIVA-C) checklist and guide

Appropriate design and reporting of superiority, equivalence and non-inferiority clinical trials incorporating a benefit-risk assessment: the BRAINS study including expert workshop

Preferred Reporting Items for Resistance Exercise Studies (PRIRES): A Checklist Developed Using an Umbrella Review of Systematic Reviews

Reporting of Factorial Randomized Trials: Extension of the CONSORT 2010 Statement

Adjusting for Treatment Switching in Oncology Trials: A Systematic Review and Recommendations for Reporting

LEVEL (Logical Explanations & Visualizations of Estimates in Linear mixed models): recommendations for reporting multilevel data and analyses

Expert consensus document: Reporting checklist for quantification of pulmonary congestion by lung ultrasound in heart failure

Best practice guidelines for citizen science in mental health research: systematic review and evidence synthesis

Evaluating the quality of studies reporting on clinical applications of stromal vascular fraction: A systematic review and proposed reporting guidelines (CLINIC-STRA-SVF)

Enhancing reporting quality and impact of early phase dose-finding clinical trials: CONSORT Dose-finding Extension (CONSORT-DEFINE) guidance

Enhancing quality and impact of early phase dose-finding clinical trial protocols: SPIRIT Dose-finding Extension (SPIRIT-DEFINE) guidance

Generate Analysis-Ready Data for Real-world Evidence: Tutorial for Harnessing Electronic Health Records With Advanced Informatic Technologies

Data Processing Strategies to Determine Maximum Oxygen Uptake: A Systematic Scoping Review and Experimental Comparison with Guidelines for Reporting

Improving the Rigor of Mechanistic Behavioral Science: The Introduction of the Checklist for Investigating Mechanisms in Behavior-Change Research (CLIMBR)

Improving the Reporting of Primary Care Research: Consensus Reporting Items for Studies in Primary Care-the CRISP Statement

Checklist for studies of HIV drug resistance prevalence or incidence: rationale and recommended use

Minimal reporting guideline for research involving eye tracking (2023 edition)

Paediatric Ureteroscopy (P-URS) reporting checklist: a new tool to aid studies report the essential items on paediatric ureteroscopy for stone disease

Adult Ureteroscopy (A-URS) Checklist: A New Tool To Standardise Reporting in Endourology

Recommendations for the development, implementation, and reporting of control interventions in efficacy and mechanistic trials of physical, psychological, and self-management therapies: the CoPPS Statement

iCHECK-DH: Guidelines and Checklist for the Reporting on Digital Health Implementations

New reporting items and recommendations for randomized trials impacted by COVID-19 and force majeure events: a targeted approach

Development, explanation, and presentation of the Physical Literacy Interventions Reporting Template (PLIRT)

CORE-CERT Items as a Minimal Requirement for Replicability of Exercise Interventions: Results From Application to Exercise Studies for Breast Cancer Patients

ACURATE: A guide for reporting sham controls in trials using acupuncture

STandards for Reporting Interventions in Clinical Trials Of Tuina/Massage (STRICTOTM): Extending the CONSORT statement

The SUPER reporting guideline suggested for reporting of surgical technique

Guidelines for Reporting Outcomes in Trial Reports: The CONSORT-Outcomes 2022 Extension

Guidelines for Reporting Outcomes in Trial Protocols: The SPIRIT-Outcomes 2022 Extension

Development of the ASSESS tool: a comprehenSive tool to Support rEporting and critical appraiSal of qualitative, quantitative, and mixed methods implementation reSearch outcomes

Evidence-based statistical analysis and methods in biomedical research (SAMBR) checklists according to design features

Establishing reporting standards for participant characteristics in post-stroke aphasia research: An international e-Delphi exercise and consensus meeting

STARTER Checklist for Antimalarial Therapeutic Efficacy Reporting

Best Practice in the chemical characterisation of extracts used in pharmacological and toxicological research-The ConPhyMP-Guidelines

Advising on Preferred Reporting Items for patient-reported outcome instrument development: the PRIPROID

Recommendations for reporting the results of studies of instrument and scale development and testing

Methodical approaches to determine the rate of radial muscle displacement using tensiomyography: A scoping review and new reporting guideline

The DoCTRINE Guidelines: Defined Criteria To Report INnovations in Education

Development of guidelines to reduce, handle and report missing data in palliative care trials: A multi-stakeholder modified nominal group technique

The RIPI-f (Reporting Integrity of Psychological Interventions delivered face-to-face) checklist was developed to guide reporting of treatment integrity in face-to-face psychological interventions

The Intraoperative Complications Assessment and Reporting with Universal Standards (ICARUS) Global Surgical Collaboration Project: Development of Criteria for Reporting Adverse Events During Surgical Procedures and Evaluating Their Impact on the Postoperative Course

CODE-EHR best-practice framework for the use of structured electronic health-care records in clinical research

TIDieR-telehealth: precision in reporting of telehealth interventions used in clinical trials – unique considerations for the Template for the Intervention Description and Replication (TIDieR) checklist

Towards better reporting of the proportion of days covered method in cardiovascular medication adherence: A scoping review and new tool TEN-SPIDERS

Position Statement on Exercise Dosage in Rheumatic and Musculoskeletal Diseases: The Role of the IMPACT-RMD Toolkit

A checklist for assessing the methodological quality of concurrent tES-fMRI studies (ContES checklist): a consensus study and statement

The Chest Wall Injury Society Recommendations for Reporting Studies of Surgical Stabilization of Rib Fractures

International Consensus Based Review and Recommendations for Minimum Reporting Standards in Research on Transcutaneous Vagus Nerve Stimulation (Version 2020)

Refining the CRiSPHe (checklist for reporting research using a simulated patient methodology in Health): a Delphi study

Conceptual Ambiguity Surrounding Gamification and Serious Games in Health Care: Literature Review and Development of Game-Based Intervention Reporting Guidelines (GAMING)

Improving Reporting of Clinical Studies Using the POSEIDON Criteria: POSORT Guidelines

Six practical recommendations for improved implementation outcomes reporting

EVIDENCE Publication Checklist for Studies Evaluating Connected Sensor Technologies: Explanation and Elaboration

Using qualitative research to develop an elaboration of the TIDieR checklist for interventions to enhance vaccination communication: short report

Preliminary Minimum Reporting Requirements for In-Vivo Neural Interface Research: I. Implantable Neural Interfaces

A Scoping Review of Four Decades of Outcomes in Nonsurgical Root Canal Treatment, Nonsurgical Retreatment, and Apexification Studies: Part 3-A Proposed Framework for Standardized Data Collection and Reporting of Endodontic Outcome Studies

Smartphone-Delivered Ecological Momentary Interventions Based on Ecological Momentary Assessments to Promote Health Behaviors: Systematic Review and Adapted Checklist for Reporting Ecological Momentary Assessment and Intervention Studies

Development of the CLARIFY (CheckList stAndardising the Reporting of Interventions For Yoga) guidelines: a Delphi study

Early phase clinical trials extension to guidelines for the content of statistical analysis plans

PRESENT 2020: Text Expanding on the Checklist for Proper Reporting of Evidence in Sport and Exercise Nutrition Trials

Checklist for Theoretical Report in Epidemiological Studies (CRT-EE): explanation and elaboration

Extending the CONSORT Statement to moxibustion

Guidelines for cellular and molecular pathology content in clinical trial protocols: the SPIRIT-Path extension

A Guideline for Reporting Mediation Analyses of Randomized Trials and Observational Studies: The AGReMA Statement

Social Innovation For Health Research (SIFHR): Development of the SIFHR Checklist

REPORT-PFP: a consensus from the International Patellofemoral Research Network to improve REPORTing of quantitative PatelloFemoral Pain studies

Journal article reporting standards for quantitative research in psychology: The APA Publications and Communications Board task force report

Guidelines for Reporting Trial Protocols and Completed Trials Modified Due to the COVID-19 Pandemic and Other Extenuating Circumstances: The CONSERVE 2021 Statement

Describing deprescribing trials better: an elaboration of the CONSORT statement

Comprehensive reporting of pelvic floor muscle training for urinary incontinence: CERT-PFMT

The APOSTEL 2.0 Recommendations for Reporting Quantitative Optical Coherence Tomography Studies

Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)

CONSORT extension for the reporting of randomised controlled trials conducted using cohorts and routinely collected data (CONSORT-ROUTINE): checklist with explanation and elaboration

EULAR recommendations for the reporting of ultrasound studies in rheumatic and musculoskeletal diseases (RMDs)

Strengthening tRansparent reporting of reseArch on uNfinished nursing CARE: The RANCARE guideline

Defining Group Care Programs: An Index of Reporting Standards

STrengthening the Reporting Of Pharmacogenetic Studies: Development of the STROPS guideline

TIDieR-Placebo: a guide and checklist for reporting placebo and sham controls

Guidelines for clinical trial protocols for interventions involving artificial intelligence: the SPIRIT-AI Extension

Reporting guidelines for clinical trial reports for interventions involving artificial intelligence: the CONSORT-AI Extension

The IDEAL Reporting Guidelines: A Delphi Consensus Statement Stage specific recommendations for reporting the evaluation of surgical innovation

The adaptive designs CONSORT extension (ACE) statement: a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design

Consensus on the reporting and experimental design of clinical and cognitive-behavioural neurofeedback studies (CRED-nf checklist)

PRIRATE 2020 guidelines for reporting randomized trials in Endodontics: a consensus-based development

Guidance for reporting intervention development studies in health research (GUIDED): an evidence-based consensus study

Standard Protocol Items for Clinical Trials with Traditional Chinese Medicine 2018: Recommendations, Explanation and Elaboration (SPIRIT-TCM Extension 2018)

SPIRIT extension and elaboration for n-of-1 trials: SPENT 2019 checklist

Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement

PaCIR: A tool to enhance pharmacist patient care intervention reporting

Criteria for describing and evaluating training interventions in healthcare professions – CRe-DEPTH

CONSORT extension for reporting N-of-1 trials for traditional Chinese medicine (CENT for TCM): Recommendations, explanation and elaboration

Consolidated criteria for strengthening reporting of health research involving indigenous peoples: the CONSIDER statement

Checklist for the preparation and review of pain clinical trial publications: a pain-specific supplement to CONSORT

CONSORT 2010 statement: extension to randomised crossover trials

Reporting of Multi-Arm Parallel-Group Randomized Trials: Extension of the CONSORT 2010 Statement

Microbiology Investigation Criteria for Reporting Objectively (MICRO): a framework for the reporting and interpretation of clinical microbiology data

Reporting of stepped wedge cluster randomised trials: extension of the CONSORT 2010 statement with explanation and elaboration

Systems Perspective of Amazon Mechanical Turk for Organizational Research: Review and Recommendations

ESPACOMP Medication Adherence Reporting Guideline (EMERGE)

Reporting randomised trials of social and psychological interventions: the CONSORT-SPI 2018 Extension

Reporting guidelines for implementation research on nurturing care interventions designed to promote early childhood development

TIDieR-PHP: a reporting guideline for population health and policy interventions

Guidelines for Inclusion of Patient-Reported Outcomes in Clinical Trial Protocols: The SPIRIT-PRO Extension

Improving the Development, Monitoring and Reporting of Stroke Rehabilitation Research: Consensus-Based Core Recommendations from the Stroke Recovery and Rehabilitation Roundtable

Variability in the Reporting of Serum Urate and Flares in Gout Clinical Trials: Need for Minimum Reporting Requirements

Methodology of assessment and reporting of safety in anti-malarial treatment efficacy studies of uncomplicated falciparum malaria in pregnancy: a systematic literature review

Standards for UNiversal reporting of patient Decision Aid Evaluation studies: the development of SUNDAE Checklist

Guidelines for the Content of Statistical Analysis Plans in Clinical Trials

RECORDS: Improved reporting of Monte Carlo Radiation transport studies: Report of the AAPM Research Committee Task Group 268

CONSORT-Equity 2017 extension and elaboration for better reporting of health equity in randomised trials

Characteristics of funding of clinical trials: cross-sectional survey and proposed guidance

GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research

Improving the reporting of clinical trials of infertility treatments (IMPRINT): modifying the CONSORT statement

Improving the reporting of therapeutic exercise interventions in rehabilitation research

A literature review of applied adaptive design methodology within the field of oncology in randomised controlled trials and a proposed extension to the CONSORT guidelines

Minimum Information for Studies Evaluating Biologics in Orthopaedics (MIBO): Platelet-Rich Plasma and Mesenchymal Stem Cells

CONSORT 2010 statement: extension checklist for reporting within person randomised trials

CONSORT Extension for Chinese Herbal Medicine Formulas 2017: Recommendations, Explanation, and Elaboration

CONSORT 2025 Statement: updated guideline for reporting randomised trials

STARD 2015: An Updated List of Essential Items for Reporting Diagnostic Accuracy Studies

SPIRIT 2025 Statement: Defining standard protocol items for clinical trials

Best Practices in Data Analysis and Sharing in Neuroimaging using MRI

Clarity in Reporting Terminology and Definitions of Set End Points in Resistance Training

An introduction to using Bayesian linear regression with clinical data

Guideline for Reporting Interventions on Spinal Manipulative Therapy: Consensus on Interventions Reporting Criteria List for Spinal Manipulative Therapy (CIRCLe SMT)

STARD-BLCM: Standards for the Reporting of Diagnostic accuracy studies that use Bayesian Latent Class Models

Standards for Reporting Implementation Studies (StaRI) Statement

Consensus on Exercise Reporting Template (CERT): Modified Delphi Study

CONSORT 2010 statement: extension to randomised pilot and feasibility trials

Core Outcome Set-STAndards for Reporting: The COS-STAR Statement

Improving the reporting quality of nonrandomized evaluations of behavioral and public health interventions: the TREND statement

Evaluation of response after pre-operative radiotherapy in soft tissue sarcomas; the European Organisation for Research and Treatment of Cancer-Soft Tissue and Bone Sarcoma Group (EORTC-STBSG) and Imaging Group recommendations for radiological examination and reporting with an emphasis on magnetic resonance imaging

Standardization of pathologic evaluation and reporting of postneoadjuvant specimens in clinical trials of breast cancer: recommendations from an international working group

Recommendations for improving the quality of reporting clinical electrochemotherapy studies based on qualitative systematic review

METastasis Reporting and Data System for Prostate Cancer: Practical Guidelines for Acquisition, Interpretation, and Reporting of Whole-body Magnetic Resonance Imaging-based Evaluations of Multiorgan Involvement in Advanced Prostate Cancer

Eliciting the child’s voice in adverse event reporting in oncology trials: Cognitive interview findings from the Pediatric Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events initiative

Recommendations to improve adverse event reporting in clinical trial publications: a joint pharmaceutical industry/journal editor perspective

Development and validation of the guideline for reporting evidence-based practice educational interventions and teaching (GREET)

Using theory of change to design and evaluate public health interventions: a systematic review

Reporting Guidelines for Health Care Simulation Research: Extensions to the CONSORT and STROBE Statements

Medical abortion reporting of efficacy: the MARE guidelines.

The Single-Case Reporting Guideline In BEhavioural Interventions (SCRIBE) 2016 Statement

Consensus on Recording Deep Endometriosis Surgery: the CORDES statement

Developing the Clarity and Openness in Reporting: E3-based (CORE) reference user manual for creation of clinical study reports in the era of clinical trial transparency

Definition and classification of intraoperative complications (CLASSIC): Delphi study and pilot evaluation

Standardized outcomes reporting in metabolic and bariatric surgery

Consensus guidelines on plasma cell myeloma minimal residual disease analysis and reporting

DELTA2 guidance on choosing the target difference and undertaking and reporting the sample size calculation for a randomised controlled trial

Guidelines for reporting of health interventions using mobile phones: mobile health (mHealth) evidence reporting and assessment (mERA) checklist

Quality of pain intensity assessment reporting: ACTTION systematic review and recommendations

An extension of STARD statements for reporting diagnostic accuracy studies on liver fibrosis tests: the Liver-FibroSTARD standards

Reporting guidelines for population pharmacokinetic analyses

Recommendations for the improved effectiveness and reporting of telemedicine programs in developing countries: results of a systematic literature review

Guidelines for the reporting of treatment trials for alcohol use disorders

A review of 40 years of enteric antimicrobial resistance research in Eastern Africa: what can be done better?

Ensuring consistent reporting of clinical pharmacy services to enhance reproducibility in practice: an improved version of DEPICT

Utstein-style guidelines on uniform reporting of in-hospital cardiopulmonary resuscitation in dogs and cats

Guidelines for reporting embedded recruitment trials

A checklist to improve reporting of group-based behaviour-change interventions

The CONSORT Statement: Application within and adaptations for orthodontic trials

Standards of reporting for MRI-targeted biopsy studies (START) of the prostate: recommendations from an International Working Group

Translating trial-based molecular monitoring into clinical practice: importance of international standards and practical considerations for community practitioners

CONSORT extension for reporting N-of-1 trials (CENT) 2015 Statement

Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews

Developing a guideline to standardize the citation of bioresources in journal articles (CoBRA)

Reporting Guidelines for Clinical Pharmacokinetic Studies: The ClinPK Statement

Using the spinal cord injury common data elements

Instrumental variable methods in comparative safety and effectiveness research

Head, neck, and brain tumor embolization guidelines

Reporting outcomes of back pain trials: a modified Delphi study

A common language in neoadjuvant breast cancer clinical trials: proposals for standard definitions and endpoints

Viscerotropic disease: case definition and guidelines for collection, analysis, and presentation of immunization safety data

Definitions, methodological and statistical issues for phase 3 clinical trials in chronic myeloid leukemia: a proposal by the European LeukemiaNet

A new standardized format for reporting hearing outcome in clinical trials

A proposed taxonomy of terms to guide the clinical trial recruitment process

Reporting standards for angiographic evaluation and endovascular treatment of cerebral arteriovenous malformations

How to report low-level laser therapy (LLLT)/photomedicine dose and beam parameters in clinical and laboratory studies

Completeness of reporting of radiation therapy planning, dose, and delivery in veterinary radiation oncology manuscripts from 2005 to 2010

Criteria for Reporting the Development and Evaluation of Complex Interventions in healthcare: revised guideline (CReDECI 2)

Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide

CONSORT Harms 2022 statement, explanation, and elaboration: updated guideline for the reporting of harms in randomized trials

Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration

Proposed best practice for statisticians in the reporting and publication of pharmaceutical industry-sponsored clinical trials

Electrodermal activity at acupoints: literature review and recommendations for reporting clinical trials

ASAS recommendations for collecting, analysing and reporting NSAID intake in clinical trials/epidemiological studies in axial spondyloarthritis

American Society of Transplantation recommendations for screening, monitoring and reporting of infectious complications in immunosuppression trials in recipients of organ transplantation

Guidelines for the reporting of renal artery revascularization in clinical trials

Reporting standards for carotid artery angioplasty and stent placement

Standardized definitions and clinical endpoints in carotid artery and supra-aortic trunk revascularization trials

Reporting standards for endovascular treatment of pulmonary embolism

Reporting Standards for Endovascular Repair of Saccular Intracranial Cerebral Aneurysms

Trial design and reporting standards for intra-arterial cerebral thrombolysis for acute ischemic stroke

Standardized reporting of bleeding complications for clinical investigations in acute coronary syndromes: a proposal from the academic bleeding consensus (ABC) multidisciplinary working group

A reporting guideline for clinical platelet transfusion studies from the BEST Collaborative

Clinical trials focusing on cancer pain educational interventions: core components to include during planning and reporting

Reporting disease activity in clinical trials of patients with rheumatoid arthritis: EULAR/ACR collaborative recommendations

Exercise therapy and low back pain: insights and proposals to improve the design, conduct, and reporting of clinical trials

Eligibility and outcomes reporting guidelines for clinical trials for patients in the state of a rising prostate-specific antigen: recommendations from the Prostate-Specific Antigen Working Group

Consensus guidelines for the conduct and reporting of clinical trials in systemic light-chain amyloidosis

Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet

Revised recommendations of the International Working Group for Diagnosis, Standardization of Response Criteria, Treatment Outcomes, and Reporting Standards for Therapeutic Trials in Acute Myeloid Leukemia

Financial Conflicts of Interest Checklist 2010 for clinical research studies

Suggestions for improving the reporting of clinical research: the role of narrative

Figures in clinical trial reports: current practice & scope for improvement

Assessing and reporting heterogeneity in treatment effects in clinical trials: a proposal

Statistics in medicine–reporting of subgroup analyses in clinical trials

Establishing a knowledge trail from molecular experiments to clinical trials

Preparing raw clinical data for publication: guidance for journal editors, authors, and peer reviewers

Guidelines for conducting and reporting mixed research in the field of counseling and beyond

Reporting experiments in homeopathic basic research (REHBaR) – a detailed guideline for authors

Guidelines for the design, conduct and reporting of human intervention studies to evaluate the health benefits of foods

Good research practices for comparative effectiveness research: Defining, reporting and interpreting nonrandomized studies of treatment effects using secondary data sources

Guidelines for reporting non-randomised studies

Setting the bar in phase II trials: the use of historical data for determining “go/no go” decision for definitive phase III testing

GNOSIS: Guidelines for Neuro-Oncology: Standards for Investigational Studies – reporting of surgically based therapeutic clinical trials

The standard of reporting of health-related quality of life in clinical cancer trials

A systematic review of the reporting of Data Monitoring Committees’ roles, interim analysis and early termination in pediatric clinical trials

CONSORT-EHEALTH: improving and standardizing evaluation reports of Web-based and mobile health interventions

Reporting of patient-reported outcomes in randomized trials: the CONSORT PRO extension

Inadequate planning and reporting of adjudication committees in clinical trials: recommendation proposal

Relevance of CONSORT reporting criteria for research on eHealth interventions

Reporting guidelines for music-based interventions

Reporting whole-body vibration intervention studies: recommendations of the International Society of Musculoskeletal and Neuronal Interactions

Reporting standards for studies of tailored interventions

Reporting data on homeopathic treatments (RedHot): A supplement to CONSORT

Evaluating the quality of reporting occupational therapy randomized controlled trials by expanding the CONSORT criteria

WIDER recommendations for reporting of behaviour change interventions

Evidence-based behavioral medicine: what is it and how do we achieve it?

The CONSORT statement checklist in allergen-specific immunotherapy: a GA2LEN paper

Improving the reporting of pragmatic trials: an extension of the CONSORT statement

CONSORT for reporting randomised trials in journal and conference abstracts

CONSORT Statement for Randomized Trials of Nonpharmacologic Treatments: A 2017 Update and a CONSORT Extension for Nonpharmacologic Trial Abstracts

Reporting randomized, controlled trials of herbal interventions: an elaborated CONSORT Statement

Consort 2010 statement: extension to cluster randomised trials

Reporting of noninferiority and equivalence randomized trials: extension of the CONSORT 2010 statement

Revised STandards for Reporting Interventions in Clinical Trials of Acupuncture (STRICTA): extending the CONSORT statement

The ORION statement: guidelines for transparent reporting of Outbreak Reports and Intervention studies Of Nosocomial infection

Consensus recommendations for the uniform reporting of clinical trials: report of the International Myeloma Workshop Consensus Panel 1

Economic evaluation alongside randomised controlled trials: design, conduct, analysis, and reporting

Guidelines for reporting results of quality of life assessments in clinical trials

GNOSIS: guidelines for neuro-oncology: standards for investigational studies-reporting of phase 1 and phase 2 clinical trials