Behavioral Interventions to Target Self-Control

Tobacco Smoking Clinical Trial

Official title:

Behavioral Interventions to Target Self-Control in Abstinent Nicotine Dependent Smokers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02281942
• Other study ID #: 1R21DA035877-01A1
• Status: Completed
• Phase: N/A
• First received: October 29, 2014
• Last updated: September 22, 2017
• Start date: May 2014
• Est. completion date: May 2017

Study information

• Verified date: September 2017
• Source: Oregon Health and Science University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Low self-control has been associated with a number of unhealthy behaviors with low treatment success. Alternative non-pharmacological approaches have the potential for enhancing self-control. This pilot study will investigate if the practice of yoga and/or health and wellness education improve self-control in the context of nicotine addiction, and will set the stage for larger clinical trials using behavioral interventions to supplement or replace existing treatments and increase the rates of recovery from disorders in which low self-control is a susceptibility factor.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 39
• Est. completion date: May 2017
• Est. primary completion date: May 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• should smoke a minimum of 10 cigarettes/day

• be fluent speaking and reading English

• in good physical health

• intend to quit smoking

• capable of abstaining from smoking for 12-14 hours

• should have easy daily access to a computer and/or other internet-enabled device

Exclusion Criteria:

• current alcohol or substance use disorder (except nicotine)

• pregnancy

• history of psychosis or bipolar disorder

• current use of a behavioral or pharmacologic tobacco treatment

• any untreated medical or psychiatric condition that might compromise their safety during participation in the study (e.g. high blood pressure, diabetes, BMI >35)

Related Conditions & MeSH terms

• Tobacco Smoking

Intervention

Behavioral:
• Yoga

• Education

Locations

Country	Name	City	State
United States	Oregon Health & Science University	Portland	Oregon

Sponsors (1)

Lead Sponsor	Collaborator
Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time (minutes) to first smoke after 12-hour abstinence		Assessed 1 week after visit 1 during a 2-hour abstinence reinforcement session