NCT05578040

Brief Summary

Auricular acupressure is one of the acupuncture techniques on the ear, which is a method of impacting on acupoints with force and without using needles to help diagnose and treat physical and psychosomatic dysfunctions. Some studies prove that the acupoints on the pinna have a corresponding relationship with the areas of the body, and when acting on the acupoints can change the temperature of the corresponding area. Chronic neck pain is closely related to the decline in subcutaneous microcirculation, where heat transfer from deep within the body to the surface of the skin is carried out by the dermal vascular system. When blood flow through the venous network is high, heat is carried from the deep to the skin and vice versa. Therefore, to understand the role of cervical vertebra acupoints in neck pain, the study wants to demonstrate the correlation when auricular acupressure at cervical vertebra acupoints and the skin surface temperature of the neck area.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P50-P75 for not_applicable healthy-volunteers

Timeline
Completed

Started Oct 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2022

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

October 10, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 13, 2022

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2023

Completed
Last Updated

October 23, 2023

Status Verified

October 1, 2023

Enrollment Period

9 months

First QC Date

October 10, 2022

Last Update Submit

October 18, 2023

Conditions

Keywords

Auricular Acupressure

Outcome Measures

Primary Outcomes (2)

  • Survey the change in temperature in the neck area respectively when auricular acupressure is applied to the left and right cervical vertebra acupoints compared with the sham auricular acupressure group

    During procedure

  • Change the temperature of skin surface in the neck area when using auricular acupressure at cervical vertebra acupoints on each side of the ear

    During procedure

Study Arms (2)

Group A: Left AH13 acupoint (left cervical vertebra)

EXPERIMENTAL

Participants received sham auricular acupressure by adhesive patches without Vaccaria seed at the left auricular cervical vertebra acupoint and auricular acupressure Vaccaria seed at the left auricular cervical vertebra acupoint after 1 week. At each time, the skin surface temperature of the neck area will be recorded.

Procedure: Auricular acupressure

Group B: RIght AH13 acupoint (right cervical vertebra)

EXPERIMENTAL

Participants received sham auricular acupressure by adhesive patches without Vaccaria seed at the right auricular cervical vertebra acupoint - and auricular acupressure Vaccaria seed at the right auricular cervical vertebra acupoint after 1 week. At each time, the skin surface temperature in the neck area will be recorded.

Procedure: Auricular acupressure

Interventions

To conduct this intervention, we used adhesive patches without Vaccaria seed to sham auricular acupressure at the cervical vertebra acupoint in the first trial phase and auricular acupressure at the cervical vertebra acupoint in the other two trial phases in 2 groups of auricular acupressure acupoints of the left and right cervical vertebra.

Group A: Left AH13 acupoint (left cervical vertebra)Group B: RIght AH13 acupoint (right cervical vertebra)

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy volunteers, regardless of gender or profession
  • Age between enough 18 and 30 years old.
  • No psychological problems (anxiety, depression, stress): assessed according to DASS 21 score, with stress score \< 15 points.
  • Vital signs within normal limits:
  • Heart rates from 60 to 100 beats/minute
  • Systolic blood pressure between 90 and 139 mmHg
  • Diastolic blood pressure between 60 and 89 mmHg
  • Body temperature: 36.59 ± 0.43 0C
  • Breathing rate: 16 ± 3 times/minute
  • Voluntarily agree to participate in the research and sign the consent form to participate in the research after being advised by the researcher and clearly explaining the rights and obligations when participating in the research.
  • Not currently participating in other intervention studies.
  • No knowledge and experience of auricular acupressure method.

You may not qualify if:

  • Having an inflammatory injury in the site of the skin to be investigated.
  • Using heat therapy, for example, massage, cupping therapy, and acupuncture in the site of the skin to be investigated within 24h.
  • Applying chemical or pharmaceutical products to the site of the skin to be surveyed before conducting the study.
  • Other diseases that could affect or interfere with outcomes, including the common cold or flu.
  • Having neck pain, dermatitis, skin infection, and wound in the survey area.
  • Having diseases that change the body temperature, like hyperthyroidism, and hypothyroidism.
  • Taking stimulants (alcohol, beer, coffee, tobacco) within 24h.
  • Staying up at night or having insomnia before the day of the study.
  • Playing sport within 2h.
  • Pregnant woman or woman in the period.
  • Are taking some sleeping pills, sedatives, or drugs that cause vasodilation, lower blood pressure
  • Anxiety, depression, and stress before conducting the study with DASS 21 score \> 15 points.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Traditional medicine - University of Medicine and Pharmacy of Ho Chi Minh City

Ho Chi Minh City, Vietnam

Location

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: A randomized controlled and single blinded trial
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Medical Doctor

Study Record Dates

First Submitted

October 10, 2022

First Posted

October 13, 2022

Study Start

October 1, 2022

Primary Completion

June 30, 2023

Study Completion

June 30, 2023

Last Updated

October 23, 2023

Record last verified: 2023-10

Data Sharing

IPD Sharing
Will share

Demographic characteristic and outcome data will be shared

Shared Documents
STUDY PROTOCOL, ICF, CSR

Locations