Item | Detail |
---|---|
1.Acupuncture rationale | 1a) Style of acupuncture |
- electro-acupuncture | |
1b) Reasoning for treatment provided, based on historical context, literature sources, and/or consensus methods, with references where appropriate | |
- electro-acupuncture treatment based on the theory of TCM, literature sources, and clinical experience in acupuncture and CINV, such as references [16] and [17]. | |
1c) Extent to which treatment was varied | |
- The treatment was not varied. | |
2. Details of needling | 2a) Number of needle insertions per subject per session (mean and range where relevant) |
- From 2 to 3. | |
2b) Names (or location if no standard name) of points used (uni/bilateral) | |
- Four points used: ST36 (bilateral); PC6 (bilateral) ;CV12(unilateral); CV13 (unilateral). | |
2c) Depth of insertion, based on a specified unit of measurement, or on a particular tissue level | |
- PC6: 0.5 body-inches; ST36: 1-1.5 body-inches; CV12 and CV13: 1-1.5 body-inches. | |
2d) Response sought (e.g., de qi or muscle twitch response) | |
- ‘De qi’ sensation will be achieved by lifting and thrusting combined with twirling and rotating the needles. | |
2e) Needle stimulation (e.g., manual, electrical) | |
- Electrical stimulation: the frequency is 2/10 Hz, and the intensity of stimulation is adjusted according to the patient’s tolerance (maximum of 10 mA). | |
2f) Needle retention time | |
- Thirty minutes | |
2g) Needle type (diameter, length, and manufacturer or material) | |
- A disposable stainless steel acupuncture needle, 0.25mm × 40 mm (Huatuo, Suzhou Medical Co. Ltd., Jiangsu, China). | |
3.Treatment regimen | 3a) Number of treatment sessions |
- Four treatment sessions in acupuncture groups. | |
3b) Frequency and duration of treatment sessions | |
- Once daily for 4 days, 30 minutes for each session. | |
4. Other components of treatment | 4a) Details of other interventions administered to the acupuncture group (e.g., moxibustion, cupping, herbs, exercises, lifestyle advice) |
- No other interventions. | |
4b) Setting and context of treatment, including instructions to practitioners, and information and explanations to patients | |
- University hospitals. - Participants will be informed about acupuncture treatment in the study as follows: “In this study, eletroacupuncture for CINV will be used based on traditional Chinese medicine.” | |
5.Practitioner background | 5) Description of participating acupuncturists (qualification or professional affiliation, years in acupuncture practice, other relevant experience) |
- The participating acupuncturists have all majored in acupuncture, have an acupuncture degree, and are qualified doctors of Tradition Chinese Medicine. All have at least 3 years of experience, and will have been trained in the standard operating procedure of electro-acupuncture on CINV. Thus, they are able to provide identical acupuncture treatment in accordance with a pre-defined protocol. | |
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 |
- The control group is supplied with standard antiemetic alone, so as to provide patients with conventional treatment for CINV. | |
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. | |
- Participants in the control group will not receive acupuncture treatment. |