Table 1. STRICTA 2010 checklist of information to include when reporting interventions in a clinical trial of acupuncture.
Item | Detail |
1. Acupuncture rationale | 1a) Style of acupuncture (e.g. Traditional Chinese Medicine, Japanese, Korean, Western medical, Five Element, ear acupuncture, etc) |
1b) Reasoning for treatment provided, based on historical context, literature sources, and/or consensus methods, with references where appropriate | |
1c) Extent to which treatment was varied | |
2. Details of needling | 2a) Number of needle insertions per subject per session (mean and range where relevant) |
2b) Names (or location if no standard name) of points used (uni/bilateral) | |
2c) Depth of insertion, based on a specified unit of measurement, or on a particular tissue level | |
2d) Response sought (e.g. de qi or muscle twitch response) | |
2e) Needle stimulation (e.g. manual, electrical) | |
2f) Needle retention time | |
2g) Needle type (diameter, length, and manufacturer or material) | |
3. Treatment regimen | 3a) Number of treatment sessions |
3b) Frequency and duration of treatment sessions | |
4. Other components of treatment | 4a) Details of other interventions administered to the acupuncture group (e.g. moxibustion, cupping, herbs, exercises, lifestyle advice) |
4b) Setting and context of treatment, including instructions to practitioners, and information and explanations to patients | |
5. Practitioner background | 5) Description of participating acupuncturists (qualification or professional affiliation, years in acupuncture practice, other relevant experience) |
6. Control or comparator interventions | 6a) Rationale for the control or comparator in the context of the research question, with sources that justify this choice |
6b) Precise description of the control or comparator. If sham acupuncture or any other type of acupuncture-like control is used, provide details as for Items 1 to 3 above. |
Note: This checklist, which should be read in conjunction with the explanations of the STRICTA items provided in the main text, is designed to replace CONSORT 2010's item 5 when reporting an acupuncture trial.