NCT05279404

Brief Summary

Acupuncture have been used in clinical treatment of diseases for at least 3,000 years, and the efficacy of acupuncture has been recognized by countries all over the world. However, most of the selected points for acupuncture treatment of diseases are based on ancient books or inheritance of experience. For example, the " Shizong Acupoint Ballad " of acupuncture records: "Neiguan (PC6) care about the chest and stomach", that is, acupuncture Neiguan can be used to treat chest, heart and stomach diseases. However, there is no scientific evidence to verify this argument so far that the Shizong Acupoint Ballad mentions "Neiguan care for the chest and stomach", and that means that Neiguan acupoint can treat the diseases of cardiovascular system and gastrointestinal system. The purpose is to verify the argument of "Neiguan care about the chest and stomach", and design a clinical trial of the Neiguan and Jianshi (PC5) on both sides of the electroacupuncture (EA) to simultaneously evaluate the heart and stomach functions. We designed a crossover test; total 72 subjects randomly equally divide the into a sham group (sham electroacupuncture) and an EA group \[2Hz EA (PC6 is cathode) and PC5 is anode\]. At least one week of washing time, then the EA group changed to a sham group and the sham group changed to an EA group. In this study, it is expected that the EA at PC6 and PC5 will affect the heart function and the function of the stomach at the same time, verifying the argument that "the PC6 care of the chest and stomach" recorded in the Shizong Acupoint Ballad.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2022

Shorter than P25 for not_applicable

Status
unknown

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

First Submitted

Initial submission to the registry

January 24, 2022

Completed
2 months until next milestone

First Posted

Study publicly available on registry

March 15, 2022

Completed
1 month until next milestone

Study Start

First participant enrolled

April 15, 2022

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2022

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2022

Completed
Last Updated

March 15, 2022

Status Verified

March 1, 2022

Enrollment Period

8 months

First QC Date

January 24, 2022

Last Update Submit

March 14, 2022

Conditions

Outcome Measures

Primary Outcomes (12)

  • Cardiac Function

    Evaluation of cardiac function with the "Osypka" non-invasive cardiac output monitor before electroacupuncture interventions . Cardiac function (OSCAR, non-invasive cardiac output meter) is first recorded for 30 minutes, and then intervention (electroacupuncture) is implemented, and cardiac function is recorded at the same time.

    thirty minutes.

  • Cardiac Function

    Evaluation of cardiac function with the "Osypka" non-invasive cardiac output monitor during electroacupuncture interventions. Cardiac function (OSCAR, non-invasive cardiac output meter) is first recorded for 30 minutes, and then intervention (electroacupuncture) is implemented, and cardiac function is recorded at the same time.

    thirty minutes.

  • Cardiac Function

    Evaluation of cardiac function with the "Osypka" non-invasive cardiac output monitor after electroacupuncture interventions. Cardiac function (OSCAR, non-invasive cardiac output meter) is first recorded for 30 minutes, and then intervention (electroacupuncture) is implemented, and cardiac function is recorded at the same time.

    thirty minutes.

  • Cardiac Function

    After at least one week (washing time), the two groups would be switched, and cardiac function is measured once in the same pattern. Evaluation of cardiac function with the "Osypka" non-invasive cardiac output monitor before sham electroacupuncture interventions. Cardiac function (OSCAR, non-invasive cardiac output meter) is first recorded for 30 minutes, and then intervention (sham electroacupuncture) is implemented, and cardiac function is recorded at the same time.

    thirty minutes.

  • Cardiac Function

    After at least one week (washing time), the two groups would be switched, and cardiac function is measured once in the same pattern. Evaluation of cardiac function with the "Osypka" non-invasive cardiac output monitor during sham electroacupuncture interventions. Cardiac function (OSCAR, non-invasive cardiac output meter) is first recorded for 30 minutes, and then intervention (sham electroacupuncture) is implemented, and cardiac function is recorded at the same time.

    thirty minutes.

  • Cardiac Function

    After at least one week (washing time), the two groups would be switched, and cardiac function is measured once in the same pattern. Evaluation of cardiac function with the "Osypka" non-invasive cardiac output monitor after sham electroacupuncture interventions. Cardiac function (OSCAR, non-invasive cardiac output meter) is first recorded for 30 minutes, and then intervention (sham electroacupuncture) is implemented, and cardiac function is recorded at the same time.

    thirty minutes.

  • Gastric Function

    Evaluation of gastric electrical rhythm with electrogastrography before electroacupuncture interventions. Gastric function (electrogastrography) is first recorded for 30 minutes, and then intervention (electroacupuncture) is implemented, and gastric function is recorded at the same time.

    thirty minutes.

  • Gastric Function

    Evaluation of gastric electrical rhythm with electrogastrography during electroacupuncture interventions. Gastric function (electrogastrography) is first recorded for 30 minutes, and then intervention (electroacupuncture) is implemented, and gastric function is recorded at the same time.

    thirty minutes.

  • Gastric Function

    Evaluation of gastric electrical rhythm with electrogastrography after electroacupuncture interventions. Gastric function (electrogastrography) is first recorded for 30 minutes, and then intervention (electroacupuncture) is implemented, and gastric function is recorded at the same time.

    thirty minutes.

  • Gastric Function

    After at least one week (washing time), the two groups would be switched, and cardiac function is measured once in the same pattern. Evaluation of gastric electrical rhythm with electrogastrography before electroacupuncture and sham electroacupuncture interventions. Gastric function (sham electroacupuncture) is first recorded for 30 minutes, and then intervention (sham electroacupuncture) is implemented, and gastric function is recorded at the same time.

    thirty minutes.

  • Gastric Function

    After at least one week (washing time), the two groups would be switched, and cardiac function is measured once in the same pattern. Evaluation of gastric electrical rhythm with electrogastrography during electroacupuncture and sham electroacupuncture interventions. Gastric function (sham electroacupuncture) is first recorded for 30 minutes, and then intervention (sham electroacupuncture) is implemented, and gastric function is recorded at the same time.

    thirty minutes.

  • Gastric Function

    After at least one week (washing time), the two groups would be switched, and cardiac function is measured once in the same pattern. Evaluation of gastric electrical rhythm with electrogastrography after electroacupuncture and sham electroacupuncture interventions. Gastric function (sham electroacupuncture) is first recorded for 30 minutes, and then intervention (sham electroacupuncture) is implemented, and gastric function is recorded at the same time.

    thirty minutes.

Study Arms (2)

Group A - electroacupuncture

EXPERIMENTAL

electroacupuncture group Insert stainless steel acupuncture needles into Neiguan (cathode) and Jianshi (anode) on both sides and twist the needles. After that, the electroacupuncture machine was connected and 2 Hz electrical stimulation was administered for 30 minutes. The stimulation intensity was mainly based on slight muscle contractions and no pain in the subjects. At this time, cardiac function and electrogastrogram were recorded at the same time.

Other: electroacupuncture

Group B - Sham electroacupuncture

SHAM COMPARATOR

Sham electroacupuncture group The method was the same as that of the electroacupuncture group, but the needles were only acupuncture under the skin of Neiguan and Jianshi without twisting the needles. The electroacupuncture machine was connected but no electrical stimulation was administered.

Other: electroacupuncture

Interventions

Electroacupuncture at Neiguan and Jianshi acupoint

Also known as: acupuncture
Group A - electroacupunctureGroup B - Sham electroacupuncture

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • (1) Normal and healthy participants
  • (2) Male or female
  • (3) The age range is 20 to 40 years old.
  • (4) Those who participates and signs informed consent after explaining the research purpose and process in detail.

You may not qualify if:

  • (1) Those with serious diseases, such as heart failure, chronic failure or cancer patients, etc.
  • (2) Those who are allergic to stainless steel needles for acupuncture.
  • (3) Pregnant or breastfeeding
  • (4) Those who are taking medicines or food such as coffee, etc. that will affect heart function such as heart rate, or gastric peristalsis.
  • (5) Unable to cooperate with researchers such as mental instability.
  • (6) Those who do not sign the consent form.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

ElectroacupunctureAcupuncture Therapy

Intervention Hierarchy (Ancestors)

Combined Modality TherapyTherapeuticsComplementary TherapiesElectric Stimulation TherapyPhysical Therapy ModalitiesRehabilitationTranscutaneous Electric Nerve StimulationAnalgesiaAnesthesia and AnalgesiaAnesthesia

Central Study Contacts

Ching-Liang Hsieh

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 24, 2022

First Posted

March 15, 2022

Study Start

April 15, 2022

Primary Completion

December 1, 2022

Study Completion

December 31, 2022

Last Updated

March 15, 2022

Record last verified: 2022-03

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) would be protected.