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Auriculotherapy effectiveness in reducing smoking

Auriculotherapy effectiveness in reducing smoking

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3xktv5
Enrollment
Unknown
Registered
2013-12-09
Start date
2013-01-07
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tobacco Use Cessation Smoking

Interventions

Experimental group: 25 smokers will be subjected to treatment with application of auricular points Shenmen, Kidney, sympathetic, 1 Anxiety, Anxiety 2, Hunger, Thirst and Addictions. Control group: 25
Behavioural
E02.190.204
E02.190.044.133

Sponsors

Universidade Federal de Alfenas
Lead Sponsor
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Possessing 18 years of age or older; Being a smoker (daily make use of any quantity of cigarettes, including a); Present level of carbon monoxide in exhaled air (COex) above 6 ppm (parts per million). Having the desire to quit smoking; Voluntarily participate in the study with available time to commit to sessions of auriculotherapy.

Exclusion criteria

Exclusion criteria: Infection, inflammation or injury to the ear; Make use of ear piercing (except earrings normal); Make some treatment for tobacco, medicinal or not. Pregnant.

Design outcomes

Primary

MeasureTime frame
Identify smoking reduction with assessing the degree of dependence measured by the Fagerstrom Test for Nicotine Dependence and evaluation of carbon monoxide in exhaled air (measured in ppm) thru the device monoxímetro.

Secondary

MeasureTime frame
Identify the profile of nicotine dependence and to investigate the association between it and the sociodemographic variables of the population investigated.

Countries

Brazil

Contacts

Public ContactErika Chaves

Universidade Federal de Alfenas

echaves@unifal-mg.edu.br+55 (35) 3299 1380

Outcome results

None listed

Source: REBEC (via WHO ICTRP)