Table 1. Details of Treatments Based on the Standards for Reporting Interventions in Clinical Trials of Acpuncture 2010 Checklist

Item Detail Description
1) Acupuncture rationale 1a) Style of Acupuncture Electroacupuncture
1b) Reasoning for treatment provided 1) Textbook of acupuncture and moxbusition medicine2) Consensus of DKMs
1c) Extent to which treatment was varied Standardized treatment
2) Details of Acupuncture 2a) Number of needle insertions per subject per session 6-10 needles
2b) Names (or location if no standard name) of points used 1) Fixed Acupoints : ST7, ST6, LI42) Depending on the symptoms presented by the patient, the attending doctor of Korean medicine may perform additional acupuncture procedures at up to 4 acupoints at their discretion.3) In the case of lymphedema and if the subject refuses, acupuncture at acupoints near the swelling site may be omitted.
2c) Depth of insertion 5-20㎜
2d) Response sought De-qi
2e) Needle stimulation Delivering electrical stimulation at 2Hz, with the intensity adjusted such that the subject perceives the stimulation without discomfort.
2f) Needle retention time 15 min
2g) Needle type Sterilized stainless steel needle measuring 0.30㎜ in width and 30㎜ inlength (Dongbang Medical co., Boryung, Korea)
3) Treatment regimen 3a) Number of treatment sessions 8 sessions
3b) Frequency and duration of treatment sessions twice a week for 8 weeks
4) Other components of treatment 4a) Details of other interventionsadministered to theacupuncture group - Brochures related to oral hygiene education guidelines are distributed to all participants and education is provided.- Concurrent therapies that are deemed likely to influence the clinical trial evaluation indicators other than the treatments provided in this clinical trial are prohibited.
4b) Setting and context of treatment The therapist restricts all unrelated conversations with the patient beyond those necessary for treatment.
5) Practitioner background Description of participating acupuncturists A doctor of Korean medicine with over one year of clinical experience.
6) Control and comparator interventions 6a) Rationale for the control or comparator in the context of the research question, with sources that justify this choice not applicable
6c) Precise description of the control or comparator not applicable