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Quantification of Shape Changes in the Facial Region by Auricular Stimulation and Their Psychosomatic Effects

Not Applicable
Recruiting
Conditions
Healthy adult female
Registration Number
JPRN-UMIN000052640
Lead Sponsor
iigata University of Health and Welfare
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

Those who receive acupuncture to the face on a regular basis. Those who are allergic to titanium, the material used to make acupuncture needles. Those who have craniofacial diseases or dental treatments that may cause geometrical changes in the facial area.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
3D image analysis device (VECTRA Handy H2: pre- and post-treatment measurements by Canfield Scientific): weekly intervention test for 4 weeks, weekly no stimulation test, total of 8 measurements.
Secondary Outcome Measures
NameTimeMethod
Subjective changes before and after treatment (pre- and post-treatment changes in facial area points, questionnaire; name, gender, age, height, weight, date and time, before and after treatment and progress, identification of adverse events) Autonomic nervous system variability measurement: measurement with HPO-200T3 (pulse rate, %SpO2) Stress Scale (PHRF-SCL(SF): Stress Checklist Short Form)
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