Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement
Abstract Background The standards for reporting interventions in clinical trials of cupping (STRICTOC), in the form of a checklist and explanations for users, were designed to improve reporting of cupping trials, particularly the interventions, and thereby facilitating their interpretation and repli...
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doaj-71b56ce7986f4c12a5de01006bf0bf722021-01-31T16:17:38ZengBMCChinese Medicine1749-85462020-01-0115111510.1186/s13020-020-0293-2Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statementXuan Zhang0Ran Tian1Wai Ching Lam2Yuting Duan3Fan Liu4Chen Zhao5Taixiang Wu6Hongcai Shang7Xudong Tang8Aiping Lyu9Zhaoxiang Bian10Chinese Clinical Trial Registry (Hong Kong), Hong Kong Chinese Medicine Clinical Study Centre, School of Chinese Medicine, Hong Kong Baptist UniversityChinese Clinical Trial Registry (Hong Kong), Hong Kong Chinese Medicine Clinical Study Centre, School of Chinese Medicine, Hong Kong Baptist UniversityChinese Clinical Trial Registry (Hong Kong), Hong Kong Chinese Medicine Clinical Study Centre, School of Chinese Medicine, Hong Kong Baptist UniversityChinese Clinical Trial Registry (Hong Kong), Hong Kong Chinese Medicine Clinical Study Centre, School of Chinese Medicine, Hong Kong Baptist UniversityChinese Clinical Trial Registry (Hong Kong), Hong Kong Chinese Medicine Clinical Study Centre, School of Chinese Medicine, Hong Kong Baptist UniversityInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical SciencesChinese Cochrane Centre, West China Hospital, Sichuan University, China Trial Registration CenterKey Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing Dongzhimen Hospital, Beijing University of Chinese MedicineXiyuan Hospital, China Academy of Chinese Medical SciencesChinese Clinical Trial Registry (Hong Kong), Hong Kong Chinese Medicine Clinical Study Centre, School of Chinese Medicine, Hong Kong Baptist UniversityChinese Clinical Trial Registry (Hong Kong), Hong Kong Chinese Medicine Clinical Study Centre, School of Chinese Medicine, Hong Kong Baptist UniversityAbstract Background The standards for reporting interventions in clinical trials of cupping (STRICTOC), in the form of a checklist and explanations for users, were designed to improve reporting of cupping trials, particularly the interventions, and thereby facilitating their interpretation and replication. Methods A group of clinical experts, methodologists, epidemiologists, and editors has developed this STRICTOC checklist through a comprehensive process, including registration of this guideline, literature review, solicitation of comments, consensus meeting, revision, and finalization. Results The STRICTOC checklist includes 6 items and 16 sub-items, namely cupping rationale, details of cupping, treatment regimen, other components of treatment, treatment provider background, and control or comparator interventions. Illustrative examples of each item are also provided. Conclusions It is intended that the STRICTOC, in conjunction with both the main Consolidated Standards of Reporting Trials (CONSORT) Statement and extension for nonpharmacologic treatment, will raise the reporting quality of clinical trials of cupping. Trial registration We have registered this study on the Enhancing the Quality and Transparency of Health Research (EQUATOR) Network: http://www.equator-network.org/library/reporting-guidelines-under-development/reporting-guidelines-under-development-for-clinical-trials/#STRICTOC.https://doi.org/10.1186/s13020-020-0293-2CuppingCONSORT extensionRandomized controlled trialReporting guideline |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xuan Zhang Ran Tian Wai Ching Lam Yuting Duan Fan Liu Chen Zhao Taixiang Wu Hongcai Shang Xudong Tang Aiping Lyu Zhaoxiang Bian |
spellingShingle |
Xuan Zhang Ran Tian Wai Ching Lam Yuting Duan Fan Liu Chen Zhao Taixiang Wu Hongcai Shang Xudong Tang Aiping Lyu Zhaoxiang Bian Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement Chinese Medicine Cupping CONSORT extension Randomized controlled trial Reporting guideline |
author_facet |
Xuan Zhang Ran Tian Wai Ching Lam Yuting Duan Fan Liu Chen Zhao Taixiang Wu Hongcai Shang Xudong Tang Aiping Lyu Zhaoxiang Bian |
author_sort |
Xuan Zhang |
title |
Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement |
title_short |
Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement |
title_full |
Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement |
title_fullStr |
Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement |
title_full_unstemmed |
Standards for reporting interventions in clinical trials of cupping (STRICTOC): extending the CONSORT statement |
title_sort |
standards for reporting interventions in clinical trials of cupping (strictoc): extending the consort statement |
publisher |
BMC |
series |
Chinese Medicine |
issn |
1749-8546 |
publishDate |
2020-01-01 |
description |
Abstract Background The standards for reporting interventions in clinical trials of cupping (STRICTOC), in the form of a checklist and explanations for users, were designed to improve reporting of cupping trials, particularly the interventions, and thereby facilitating their interpretation and replication. Methods A group of clinical experts, methodologists, epidemiologists, and editors has developed this STRICTOC checklist through a comprehensive process, including registration of this guideline, literature review, solicitation of comments, consensus meeting, revision, and finalization. Results The STRICTOC checklist includes 6 items and 16 sub-items, namely cupping rationale, details of cupping, treatment regimen, other components of treatment, treatment provider background, and control or comparator interventions. Illustrative examples of each item are also provided. Conclusions It is intended that the STRICTOC, in conjunction with both the main Consolidated Standards of Reporting Trials (CONSORT) Statement and extension for nonpharmacologic treatment, will raise the reporting quality of clinical trials of cupping. Trial registration We have registered this study on the Enhancing the Quality and Transparency of Health Research (EQUATOR) Network: http://www.equator-network.org/library/reporting-guidelines-under-development/reporting-guidelines-under-development-for-clinical-trials/#STRICTOC. |
topic |
Cupping CONSORT extension Randomized controlled trial Reporting guideline |
url |
https://doi.org/10.1186/s13020-020-0293-2 |
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