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Search Reporting Guidelines Under Development

Title year-registered date-updated
A CONSORT extension for reporting Pragmatic and Explanatory trials designed using the PRECIS tool (CONSORT-PRECIS) 2026  
A reporting guideline for artificial intelligence-enabled simulation-based eductianl interventions in health professions education (RAISE-HPE) 2026  
A reporting guideline for research into outcomes following release from correctional and forensic settings 2026  
A reporting guideline for the use of artificial intelligence in legal research: reporting standards for legal research in which generative artificial intelligence or large language models are used (RAILS) 2026  
A reporting tool for evidence-based guidelines on Chinese medicine for public health emergencies: an extension of the RIGHT statement 2023  
AD ASTRA – SPIRIT and CONSORT extensions for dog-assisted interventions 2024  
AD-DELTA2: Guideline on the reporting of sample size in trial grant applications and protocols for adaptive design: an extension of the DELTA2 guideline 2025  
AE-ACU – Reporting guidelines for Adverse Events in ACUpuncture clinical trials 2024  
AI4HM: A Protocol Template for Observational Studies Involving Artificial Intelligence and Machine Learning in Health and Medicine 2026  
APOSTEL-AS - Advised Protocol for Optical coherence tomography (OCT) Study Terminology and Elements - extension for studies involving Anterior Segment OCT 2023  
APT-SAP: Enhancing the design, conduct and analysis of Adaptive and Platform Trials through consensus-driven Statistical Analysis Plan guidance 2025  
ARRIVE for Acupuncture – An extension of the ARRIVE Statement for Animal Research on Acupuncture 2018  
Alberta Quality Assessment Tool for Human Evaluation Studies of Large Language Model (LLM)-Based Question-Answering (QA) Systems: Reporting Checklist 2025  
BEST-CHMF – BEtter reporting of Safety assessment in clinical Trials with Chinese Herbal Medicine Formulas 2024  
BRIDGE-AI reporting guideline for cross-design evaluation studies of artificial intelligence in digital health diagnosis, clinical decision support, and post-deployment monitoring. 2026  
Blinding in Acupuncture Clinical Trials: guidelines for assessment and reporting 2024 26 November 2024
CANGARU - ChatGPT and Artificial Intelligence Natural Large Language Models for Accountable Reporting and Use Guidelines 2023  
CARITS - Complete and Accurate Reporting of Interrupted Time Series studies 2023  
CAST-D - Reporting Guideline for Case Study in Public Health and Medicine related to Disasters 2024  
CGM-REPORT: A Reporting Guideline for Studies Using Continuous Glucose Monitoring in Individuals Without Diabetes 2026  
CHAT-GUIDE: Reporting the Use of ChatGPT and Generative Artificial Intelligence (Large Language Models) in Healthcare Research and Practice 2026  
CHEERS ClimatE - Consolidated Health economic evaluation reporting standards Climate Extended 2023  
CHEERS extension for the reporting of economic evaluations of infectious disease interventions utilising epidemiological and dynamic transmission modelling (CHEERS-ID) 2026  
CINEX - a reporting guideline for clinical information extraction studies 2024  
CLARITY: CheckList for Agentic Reasoning and InTelligence in Healthcare. A reporting guideline for studies that develop, evaluate or deploy agentic artificial intelligence (AI) systems in healthcare 2026  
COMET-Bib: Comprehensive Methodological Transparency for Bibliometric Studies 2026  
CONSENS - Recommendations for improving reporting of CONtextual analySis in implEmeNtation Science 2052  
CONSORT Extension for Herbal Harms Reporting 2024  
CONSORT Extension for Multicenter Clinical Trials 2020: Recommendations, Explanation, and Elaboration 2018 9 January 2024
CONSORT Extension for TCM Pattern-Guided Same Treatment for Different Diseases Randomized Controlled Trials: the CONSORT-TCM Pattern Statement 2026  
CONSORT Social Work – Reporting Guideline for Social Work intervention trials: CONSORT Extension 2024  
CONSORT and SPIRIT Extension for Decentralized Clinical Trials (CONSORT-DCT & SPIRIT-DCT) 2026  
CONSORT and SPIRIT extensions for non-inferiority and equivalence trials 2025  
CONSORT-A 2026: Consolidated Standards of Reporting Trials for Acupuncture 2026 2025  
CONSORT-CHI: An extension of the CONSORT reporting guideline for Controlled Human Infection studies 2025  
CONSORT-Herbal 2026: CONSORT Herbal 2026 Statement: updated guideline for reporting randomised trials of medicinal plant extracts and natural products as active ingredients and finished products. 2025  
CORE: Community Engaged Research Reporting Guidelines 2025  
COREMILK: COnsensus Guidelines for REsearch on Human MILK 2025  
COREQ-LLM: Consolidated Criteria for Reporting Qualitative Research + Large Language Model Extension 2025  
CORES - CO-creation REporting Standards for research 2023  
CORMMIX - Consolidated Checklist for Reporting Mixed-Methods Research 2023  
CORTRE: COmplete Reporting for Transparency Reproducibility Efforts 2025  
CRCA&M - Consensus-Based Recommendations for Case Report in Acupuncture and Moxibustion 2022  
CRIMP - Case Reports in Mental Health and Psychiatry Reporting Guidelines 2024  
CheRIHoSS - Checklist of Reporting Items for Horizon Scanning Studies 2025  
Checklist for Reporting Valuation Studies of Multi-Attribute Utility-Based Instruments – Collaborative Involvement 2026  
Checklist for Reporting of Sample Size Determination in Randomized Controlled Trials (CROSS-RCT) 2026  
Checklist for the conduct and reporting of micro-costing studies in health care 2014 2019 and 2021
Chinese Medicine Formulas - STrengthening the Reporting of Observational Real-World Studies about Chinese Medicine Formulas: STROBE extension 2023  
Chinese Medicine Formulas Protocols - Standard Protocol Items for Observational Real-World Studies about Chinese Medicine Formulas 2023  
Community of Practice Reporting Guide for Practice and Research 2026  
Congressionally Mandated Reporting Guidelines: Enhancing Transparency and Clarity for Policy Reporting and Dissemination (CMR guidelines) 2026  
Consensus for APP Review Reporting Items (CAPPRRI) 2023 25 April 2024; 7 February 2025
Consolidated Guidelines for Reporting and Evaluation of studies using Transcranial Electrical Stimulation 2025  
Consolidated Health Economic Evaluation Reporting Standards for Screening Studies (CHEERS-SCREEN) 2025  
Consolidated reporting items for REal World Study (CREWS) 2019  
Construction of Individualized Clinical Decision Model for Single Disease with Benefit-Risk-Cost Analysis and Priority Reporting List (BEST-CDM) 2026  
DICE Checklist: a reporting guideline for strengthening diversity, inclusion, culture, and equity considerations within musculoskeletal research 2026  
DOSSIER (Documentation Of Synthetic health data: Standard Items for Evaluation and Reporting), a reporting guideline for studies that generate, use or evaluate synthetic health data 2026  
DeNote - A data note reporting guideline for qualitative health and social care research datasets 2024  
ECoHealth - Reporting Guideline for Assessments of the Environmental Consequences of Healthcare 2023  
ENLIGHT – ICU reporting checklist 2026  
ENLIGHT-Field: Field research extension of the ENLIGHT Checklist and Guidelines for daylight, electric and mixed field research 2024  
EPIC - Enhanced Prevalence and Incidence Criteria 2023  
Endoscopic Endonasal Pituitary Neuroendocrine Tumor (PitNET) Reporting Guideline: a reporting guideline for clinical and surgical outcomes of endoscopic endonasal surgery for PitNET 2026  
Evidence-Based Practice Policy Analysis and Program Evaluation Reporting Guidelines 2026  
FAIR – Fidelity to Acupuncture Intervention Reporting 2024  
FAIR Omics Reporting for Meta-Analysis 2026  
GLOBAL - Guidance List for the repOrting of Bibliometric AnaLyses 2022  
GRACE - Guidelines for the Reporting of A Clinical Electroencephalogram (EEG) in the medical literature 2023  
GRAMMS 2.0: Updating the good reporting of mixed methods study reporting guidelines 2025  
GRRAS-COSMIN: Guidelines for Reporting Reliability and Agreement Studies-Consensus-based Standards for the selection of health Measurement Instruments 2025  
GUIDE-AI - Reporting Checklist on the use of Artificial Inteligence in the Health Guideline Enterprise 2024  
GUIDE-Rehab - GUideline for Intervention DEscription in Rehabilitation 2024  
Guidance for Reporting Involvement of Patients and the Public 2 – Youth Extension (GRIPP2-Y) 2026  
Guideline for Reporting Environmental Epidemiology aNalyses (GREEN) 2016 2 November 2021
Guidelines On Assessments in LMIC Settings (GOALS) 2018  
Guidelines foR Evaluating the ENvironmental impacts of CARE pathways in healthcare (GREEN CARE) reporting guideline 2026  
Guidelines for Reporting Clinical Trials on Integrated Chinese and Western Medicine 2023 9 January 2024
Guidelines for Reporting Single Group Trial for traditional Chinese medicine with Objective Performance Criteria or Performance Goal 2022  
Guidelines for cellular and molecular pathology content in clinical trial protocols: the SPIRIT-Path extension update and remapping 2026 2026  
Guidelines for ethical review of acupuncture and moxibustion clinical research 2026  
HOTTER: Heat therapy: Optimising Transparency Through Essential Reporting 2026  
IMPACT Framework - Reporting the impact of patient and caregiver involvement in health research 2025  
INCREASE - Increasing transparency and Reproducibility of data Extraction for evidence Synthesis research 2023  
INVIRTUE - Reporting Guidelines for Virtual Reality Intervention Studies 2024  
Inclusivity Checklist for Clinical Research 2025  
Informed Methodology for Publishing Advocacy Change and Transformation 2026  
LEVERAGE - GuideLines for rEporting the deVelopment, dEliveRy and evAluation of health interventions/policies Guided by commonly used systEms approaches 2025  
LIGHTS–LAMPES: a two-level reporting guideline for clinical, laboratory and pre-clinical studies of therapeutic light-based and laser interventions in photomedicine 2026  
MARMAR-Guidelines for the measurement, analysis, and reporting of medication adherence in the run-in phase of clinical trials 2025  
MEASURE Statement - Medical Education Assessment Studies Uniform REporting statement - A reporting guideline for validity investigation studies 2020  
META-TTE - Transparent reporting of meta-analyses of time-to-event outcomes based on aggregate data from randomised trials of interventions 2023  
Medical Media Quality Reporting Guide 2026  
Minimum standards for content and format of meta-data and data reporting in systematic reviews 2020  
MuRMuR-AI - MultiReader Multicase Reporting (MuRMuR) Guidelines, including AI-Assisted Image Interpretation 2025  
NUR-Case - Nursing Case Reporting Framework 2025  
OPTIMISE-AR (incOrporating PaTIent-reported outcoMes In doSE-finding oncology trials – Analysis Recommendations) 2025  
ORIOCE - Guidelines for transparent reporting of Outbreak Reports and Intervention Of Community Epidemics 2023  
Orthopaedic CAse REport Reporting Guideline 2026  
PHENOMOVE: Phenotyping standards for reporting signs and symptoms in movement disorders 2026  
PLOT (Protocol Lab for Online Trials) 2019  
POCUS-REPORT: Reporting Guideline for Clinical and Research Studies Using Point-of-Care Ultrasound 2025  
POCUS-REPORT: The REporting a Time-to-onset Anaysis using Individual Case Safety reports in PharmacoVigilance 2025  
PRECISE - The Preferred Components for Co-design in Research 2023  
PREHOSPITAL-CARE: A consensus-based guideline for publishing pre-hospital case reports 2018  
PRINMA-A — Preferred Reporting Items for Network Meta-Analysis of Acupuncture Statement 2023  
PRISMA Extension for Systematic Reviews Using GRADE 2023  
PRISMA for NMA update - Updating PRISMA for Network meta-analysis 2024  
PRISMA-AI - Preferred Reporting Items for Systematic Reviews and Meta-Analyses - Artificial Intelligence Extension 2022  
PRISMA-EE - PRISMA guideline extension for systematic reviews of health economic evaluations 2024  
PRISMA-EGMs - PRISMA-Evidence and Gap Maps 2023  
PRISMA-P Update - Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols 2024  
PRISMA-PF - Preferred Reporting Items for Systematic Reviews and Meta-Analysis of Prognostic Factor Studies 2024  
PRISMA-QES - PRISMA Extension for Qualitative Evidence Syntheses 2022  
PRISMA-RR: an extension to PRISMA for rapid reviews 2015 June 2024
PRISMA-ScR update - Updating the PRISMA reporting guideline for scoping reviews: study protocol 2024  
PRISMA-prev - Extension of PRISMA 2020 for systematic reviews of prevalence 2023  
PRISMA-probiotics: Extension for probiotics 2025  
PRISTINE: Preferred Reporting Items for Syntheses Through Interactive, Navigable Evidence-portals 2025  
PRITEM - Preferred Reporting Items for Evidence Mapping 2022  
PRITERS - Preferred Reporting Items for Replication of Systematic Reviews 2025  
PROM-GRIP - Patient-Reported Outcome Measures - Guideline for Reporting In clinical Practice 2024  
PRe-EquiP-LMICs - Guidelines for conducting and reporting global, participatory research in Pulmonary Rehabilitation to promote Equitable Participation from Low- and Middle-Income Countries 2025  
PhyCaRe - Reporting guideline for physiotherapy case reports 2022  
Preferred Reporting Items for Measuring Exercise-induced hypoalgesia (EIH-PRIME) 2026  
Preferred Reporting Items for Systematic Reviews and Meta-Analyses - Artificial Intelligence as Method (PRISMA-AIM): a reporting guideline for AI use in systematic reviews 2026  
Preferred Reporting Items for Systematic reviews and Meta-Analyses - PRISMA Extension of Preclinical In Vivo Animal Experiments 2020  
Preferred Reporting Items for Systematic reviews and Meta-Analysis - Protocols for Children (PRISMA-PC) 2014 14 June 2022; 20 November 2024
Psychological self-Report Instruments in Databases: the PRIDE Reporting Guideline 2026  
QRDC-RG - Qualitative Remote Data Collection Reporting Guideline 2025  
QUality standards for reporting In Tobacco-intervention studies (QUIT) 2026  
RCTRaCk – Randomized Controlled Trials in Rehabilitation Checklist 2019  
RECONSIDER – Reporting extension of CONSORT and SPIRIT for Inclusion, Diversity, Ethnicity and Race 2022  
REFORH: REporting guideline For ORganoids in Human clinical studies 2026  
REFORM - REporting guideline For Organoids pRe-clinical experiMents 2025  
REporting of studies Conducted using Observational Routinely collected health Data (RECORD): updated reporting guideline for observational studies using routinely collected health data 2026  
RGAR-TCM - Reporting Guideline for Animal Research in the Field of Traditional Chinese Medicine 2023  
RIGHT 2.0: Reporting Items for practice Guidelines in HealThcare 2026  
RIGHT-MuSE: Reporting guidance for interest-holder engagement in practice guidelines 2025  
ReFiND – checklist and recommendations for evaluating and Reporting Fidelity of Non-Drug interventions 2023  
ReRT-REPORT: A cross-design reporting guideline for reirradiation studies 2026  
RepOrting standards for Systematic Evidence Syntheses (ROSES): an update to reporting standards for systematic reviews, meta-analyses, and systematic maps in environmental sciences 2026  
Reporting Elements for Foundation Models in Gastrointestinal Endoscopy (REFORM-GIE) 2026  
Reporting Guideline for Clinical Practice Guidelines for Medical Nutrition Therapy: An Extension of the RIGHT Statement 2024  
Reporting Guideline for Environmental Outcomes in Clinical Trials: CONSORT Extension 2024  
Reporting Guideline for Environmental Outcomes in Clinical Trials: SPIRIT Extension 2024  
Reporting Guideline for Mesenchymal Stromal Cells (MSC) Therapy 2021  
Reporting Guideline for the Participatory Development & Evaluation of Digital Health Interventions 2025  
Reporting Guidelines for Artificial Intelligence Research in Mental Health 2024  
Reporting Guidelines for Case Series Studies 2026  
Reporting Guidelines for Organoid-Based Clinical Trials: An Extension of the CONSORT Statement 2025  
Reporting Guidelines for Pathology in Randomised Controlled Trials (CONSORT-Path) 2020  
Reporting Guidelines for Peer-Review Publication of Community-Engaged Research (CEnR) 2026  
Reporting Guidelines for drug utilization and pharmacoepidemiological studies using the WHO ATC/DDD methodoloogy: the EMMA checklist 2026  
Reporting Items for Evidence Summary 2025  
Reporting checklist for systematic review of clinical practice guidelines: a RIGHT extension statement 2025  
Reporting guidelines for artificial intelligence (AI) and extended reality (XR) interventions in nursing research – twin reporting checklists (one for AI, one for XR) with a shared explanation-and-elaboration document (DEFINE) 2026  
Research reporting guidelines for health RESearch involving People who arE inCarceraTed: The RESPECT Guidelines 2025  
SAPI - Statistical Analysis Plan for Observational Studies with Initial Data Analysis 2024  
SAPs for CRTs – Guidelines for the Content of Statistical Analysis Plans for Cluster Randomised Trials 2023  
SEB - Standards for EEG Biomarkers 2023  
SESAME - Standard Elements in Studies of Adverse events and Medical Error 2023  
SHIME - Standards for Healthcare Impact Evaluation 2025  
SIM-TRAIN REPORT: Reporting Guideline for Simulation-Based Training, Education and Research in Medical and Health Care 2026  
SPARK - Scale Up Research Reporting Checklist 2024  
SPIRIT extension for reporting Pragmatic and Explanatory trial protocols designed using the PRECIS tool (SPIRIT-PRECIS) 2026  
SPIRIT-A 2026: (Standard Protocol Items: Recommendations for Interventional Trials) for Acupuncture 2026 2025  
SPIRIT-MCT - SPIRIT Extension for Multicenter Clinical Trials 2022 9 January 2024
SPIRIT-ROUTINE - for protocols of trials using cohorts and routinely collected data 2021  
SPRINT: Standards for Presenting and Reporting clinical InterveNtions Televisually 2023  
SPoRTIER: Social Prescribing Reporting Template to Improve Evaluation and Replication 2018  
SSG-REPORT: Reporting guideline for acute and longitudinal small-sided games studies in team sports research 2026  
STAR-MBMA - Standards for Transparent and Accurate Reporting of Model-Based Meta-Analyses - General Guideline 2024  
STARD-NBS - Standardized Reporting of Newborn Screening Outcomes 2023  
START-EDI - STAndards for ReporTing Equality, Diversity and Inclusion 2024  
STEMGEN Checklist Design for Stem Cell Differentiation and Genetic Engineering Studies 2026  
STLER: Standards for Legal Epidemiology Reporting 2025  
STRICTA Ⅲ – The Standards for Reporting Interventions in Clinical Trials of Acupuncture 2025  
STRIMAM - STandards for Reporting Interventions in Moxibustion using Animal Models 2023  
STROBE for TCM - Reporting Guideline for observational studies on Traditional Chinese Medicine (formerly Chinese Herbal Medicine Formulas) 2019  
STROBE-D: Strengthening the Reporting og Observational Studies in Epidemiology for Drowning (STROBE-D): An extension of the STROBE statement for drowning research 2025  
STROBE-MetEpi - Guidelines for Strengthening the Reporting of Metabolomic Epidemiology Studies 2021  
STROBE-Vision - an extension of the STROBE statement 2021  
STROBE-pregnancy outcomes 2020  
STROBE-prev - Strengthening the Reporting of Studies of Prevalence 2023  
SUMO-cross - Reporting cross-sectional SUrveys conducted in Multiple cOntexts (SUMO-cross) 2024  
SWAP-AI: A Reporting Guideline for Scientific Web Applications and Platforms Built with Artificial Intelligence 2026  
Sex and Gender Reporting Guidelines in Traditional Chinese Medicine Research (SGR-TCM) 2026  
StaRLiF: Standards for reporting the development and validation of literature search filters 2025  
Standardised Reporting of the Carbon Footprint of Clinical Pathways 2024  
Standardised frameworks to design and report anaesthesia interventions in clinical trials 2023  
Standardized Protocol Items: Recommendations for Observational Studies (SPIROS) 2017  
Standardizing surgical Interventions & Co-interventions; establishing quality assurance for surgical interventions in randomised controlled trials (STItCh-IT) 2016 November 2021
Standards for Reporting Interventions in Clinical Trials of Bloodletting (STRICTOB): extending the CONSORT statement 2026  
Standards for Reporting of Digital Health Education Intervention Trials (STEDI) 2017  
Standards for Transparent And complete reporting of Games in medical Education (STAGE) 2026  
Standards for Transparent reporting of Oral Health-Related Quality of life studies (STORQ) 2026  
Standards for reporting disaster health research and field operations (STARDIS) 2026  
Standards for transparent reporting of aligner treatment studies (STRAND) 2026  
Standards for transparent reporting of dental implant studies (STRIDE): 2026  
Standards of Reporting the Network Pharmacology of Chinese Medicine 2026  
Standards of reporting for studies on medical grade footwear for adults 2025  
Survey Aware Machine Learning (SaML) Statement: Reporting Items for Machine Learning Studies Using Complex Sample Survey Data 2026  
TAE-ACU - The Terminology criteria of Adverse Events for ACUpuncture 2024  
TARGET-TCM: a reporting guideline extension of the TARGET Statement for traditional Chinese medicine 2026  
THESES-M: Transparent and Holistic Evaluation Standards for Educational Studies in Medicine: A reporting guideline for medical theses 2025  
TIDIER-A 2026: TIDieR extension for acupuncture: Template for Acupuncture Intervention Description and Replication 2025  
TIDieR‑aqua: Template for the Intervention Description and Replication (TIDieR) for reporting of aquatic interventions 2025  
TRAFFIC: Reporting and conduct guideline for randomised clinical trials of fermented food interventions 2026  
TREATS-RG - Transparent Reporting for Essential oil & Aroma Therapeutic Studies—Reporting Guideline 2024  
TRIPOD-Code - a reporting guideline for code repositories associated with diagnostic and prognostic prediction model studies 2025  
TRIPOD-P: a reporting guideline for protocols of clinical prediction models/predictive AI tools 2026  
TRIPOD-PF - Reporting recommendations for diagnostic and prognostic factor studies 2021 5 February 2026
TRoCA - Transparent Reporting of Cluster Analyses 2024  
The CLAIRE statement: a comprehensive reporting and assessing guideline for artificial intelligence in diagnostic imaging 2026  
The CSS-EIC Statement: Consensus on Research Ethics and Integrity in Sports Science (Chinese Expert Consensus) 2026  
The RAPPORT Statement: Reporting Guideline for Rigor and Reproducibility in Community-engaged research 2026  
The Readability Checklist: A reporting guideline for studies assessing the readability of written health information 2026  
The Systematic Engine: A Diagnostic Reporting Guideline for Critical Appraisal Processes in Evidence Synthesis 2026  
The reporting for Chinese herbal medicine placebo guidelines in randomized controlled trials 2026  
Transparent Reporting of Adaptations, Context, and Effects 2026  
Transparent Reporting of Educational Interventions and Curriculum Research in Health Professions Education 2026  
Transparent Reporting of Educational Interventions and Curriculum Research in Health Professions Education (TEACH) 2026  
Transparent Reporting of studies developing, validating, updating or evaluating AI- and ML-based systems in the Care of Older Adults: a reporting guideline (TRAICO) 2026  
UNITE: Reporting guidelines for youth and family specific engagement in research 2025  
United Through Health (UTH) — a reporting guideline for published national calculations of the monetary cost of the between-group gap in access to health (health-economic estimates of what unequal access costs) 2026  
Universal Engagement Reporting Tool (UER) 2026  
Updating the Reporting Guidelines for Music-based Interventions 2023  
VANRA (Verification of Assertions in Narrative Review Articles): a reporting checklist for narrative review articles 2026  
VHC-TEST: a reporting guideline for bench and in vitro testing of spacers and valved holding chambers used with inhalers 2026  
WATER - Guideline for Wastewater Analysis and Tracking in Epidemiological Reporting 2025  
WHO Trial Registration Data Set (TRDS) extension for organoid studies 2026  
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