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Effectiveness of Auricular Acupressure on the Methadone Patient

N

National Taipei University of Nursing and Health Sciences

Status

Completed

Conditions

Conditions:Effectiveness of Auricular Acupressure on the Methadone Patient

Treatments

Other: Auricular pressure

Study type

Interventional

Funder types

Other

Identifiers

NCT05913830
TCHIRB-11012011

Details and patient eligibility

About

This study aims to investigate the effect of auricular point sticking on constipation in patients with methadone

Full description

This study is a randomized controlled trial, taking 72 methadone constipation patients from a hospital in the north as objects, and divided them into an auricular point group and a control group. The experimental group was given auricular point sticking, while the control group only used sticking cloth. The two groups were measured for constipation, TCM constitution, anxiety, depression and quality of life before the intervention and 2 weeks, 4 weeks, and 6 weeks after the start.

Enrollment

72 patients

Sex

All

Ages

20 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. Methadone patients over 20 years old.
  2. Those who have clear consciousness and can communicate in Chinese and Taiwanese.
  3. The frequency of defecation is less than three times a week.
  4. Willing to sign a written subject consent form.

Exclusions:

  1. Those with wounds, broken skin, and blisters on the skin of both ears.
  2. People with blood coagulation problems and related diseases, such as: purpura, hemophilia, etc.
  3. Age <20 years old.
  4. Subjects who use drugs to improve constipation.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

72 participants in 2 patient groups

Experimental group:
Experimental group
Description:
Experimental Group A total of 36 methadone patients will receive auricular pressure
Treatment:
Other: Auricular pressure
Control group:
No Intervention group
Description:
Control group 36 bits No interventions implemented

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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