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Clinical Trials in China / NCT07794995
Recruiting Not applicable

Effectiveness of an Acupressure Band for Primary Dysmenorrhea in College Students

NCT07794995 · tracked via the Priya Life Science China tracker
Sponsor
China Medical University Hospital
Phase
Not applicable
Started
2026-09-01
Last updated
2026-08-31

Condition(s) studied

Primary Dysmenorrhea (PD)

Investigational drug(s) / intervention(s)

Compression band with vaccaria seedsCompression band only

Compression band with vaccaria seeds: The intervention utilizes an adjustable band with three Vaccaria seeds forming a 5 mm circular stimulation area, designed to cover the Sanyinjiao (SP6) acupoint region. The seeds are fixed on the inner side of the band. In the first session, a medical student research assistant trained in acupuncture will teach the participant how to locate the SP6 acupoint (3 cun or 4 finger-widths above the tip of the medial malleolus, at the posterior border of the tibia). For subsequent home-based intervention, participants will locate and apply the band by themselves. The band consists of 60% non-elastic and 40% elastic materials with a 3 cm velcro buffer.

Compression band only: The control group utilizes the same adjustable band design but without any Vaccaria seeds on the inner side. In the first session, a medical student research assistant will guide the participant to locate the Sanyinjiao (SP6) region on the calf for standardization. Participants will wear and apply the band by themselves at home following the same instructions. The band consists of 60% non-elastic and 40% elastic materials, with a 3-cm Velcro buffer.

Study summary

This study aims to investigate the effectiveness of an acupressure band in improving primary dysmenorrhea among college students. Primary dysmenorrhea is characterized by cramping lower abdominal pain during menstruation and is often accompanied by symptoms such as nausea, fatigue, and headache. It is also one of the leading causes of academic and work absenteeism among women of reproductive age. Previous studies have shown that acupressure applied to the Sanyinjiao (SP6) acupoint can alleviate menstrual pain. In addition, current clinical research has mainly focused on auricular acupressure using Vaccaria seeds, while relatively few studies have explored their application on body acupoints. Therefore, this study focuses on the application of Vaccaria seeds on the Sanyinjiao (SP6) acupoint to evaluate their effects on primary dysmenorrhea.

To provide continuous and stable acupoint stimulation, this study utilizes an intervention device combining Vaccaria seeds with a compression band, together with acupressure stimulation.

This study adopts a single-blind randomized controlled trial design. A total of 30 participants will be randomly assigned to either the experimental group or the control group (compression band only group). The study consists of four menstrual cycles, including one baseline menstrual cycle followed by three consecutive menstrual cycles of home-based intervention.

Outcome measures include the Visual Analog Scale (VAS) for pain intensity, the Menstrual Distress Questionnaire (MEDI-Q) for menstrual-related symptoms and distress, and heart rate variability (HRV), monitored using the ANS Watch as an indicator of autonomic nervous system activity. Statistical analyses will be conducted to compare differences between the experimental and control groups, as well as between pre- and post-intervention measurements, in order to evaluate the clinical potential of the acupressure band for primary dysmenorrhea management.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
24 Years
Healthy volunteers
No
Inclusion Criteria: * Female university students aged 20 to 24 years. * Diagnosed with primary dysmenorrhea and having a Visual Analog Scale (VAS) pain score of 3 or higher. * Regular menstrual cycles ranging from 21 to 35 days. * Menstrual duration ranging from 4 to 10 days. Exclusion Criteria: * Known history of secondary dysmenorrhea, including endometriosis or uterine fibroids. * Chronic medical disease or psychiatric disease. * Current smoking. * Pregnancy. * Long-term use of oral contraceptives or presence of an intrauterine device. * Significant lower-extremity pitting edema, abnormal lower-extremity circulation, marked swelling, skin damage, infection, sensory abnormalities, or other conditions considered unsuitable for wearing the acupressure band by the research staff.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
China Medical University Hospital Taichung Taichung City Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07794995 on ClinicalTrials.gov ↗ ← All trials in China