Assessment of Smoking, Vaping, and Alcohol Consumption Behavior

April 15, 2021 updated by: Corby K. Martin, Pennington Biomedical Research Center

Online Survey to Assess Smoking, Vaping, and Alcohol Consumption Behavior in the Population

To assess smoking, vaping, and alcohol consumption behaviors via online surveys in the population. Further, the objective is to administer additional surveys to assess which methods (e.g., pen-and-paper records, a smartphone app) for monitoring smoking, vaping, alcohol intake, and food intake are preferred by the study population.

Study Overview

Detailed Description

Many smokers believe that smoking helps them to control their weight, and concerns about weight gain can interfere with smoking cessation. In fact, nicotine has been shown to suppress appetite and increase resting metabolic rate, and smoking also serves as a behavioral alternative to eating or a distraction from hunger or food cravings. E-cigarettes are frequently marketed as the safer and healthier alternative to smoking, and some e-cigarettes are in fact actively advertised for weight management and/or suppression of food cravings, encouraging smokers to make the switch. In contrast, alcohol consumption has been shown to increase appetite and food intake and at the same time is associated with smoking and vaping.

Therefore, it is possible that participants who smoke or vape for weight control, particularly those who also regularly consume alcohol, would benefit from a lifestyle program that encompasses dietary counseling and exercise to prevent weight gain after smoking cessation. Additionally, methods to assess smoking, vaping, alcohol intake, and food intake (i.e., ingestive behaviors) historically relied on self-report, though the investigator's group has developed smartphone apps that allow people to capture images of their intake and/or self-report their intake in the app. App-based methods offer advantages, including the real-time transfer of data, and it is presumed that people will believe that apps are an easier and preferred method to capture ingestive behaviors, yet this assumption has not yet been thoroughly examined.

Study Type

Observational

Enrollment (Actual)

3245

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Louisiana
      • Baton Rouge, Louisiana, United States, 70806
        • Pennington Biomedical Research Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Individuals aged 18 to 85 years who regularly engage in one or more of the following behaviors:

  • cigarette smoking
  • e-cigarette consumption (vaping)
  • alcohol consumption

Description

Inclusion Criteria:

  • Individuals aged 18 to 85 years are eligible to complete the Demographics Questionnaire and the Food Intake Assessment Preference Questionnaire.
  • Individuals in the same age range who regularly smoke cigarettes can complete the Smoking Questionnaire and the Smoking Assessment Preference Questionnaire, in addition to the Demographics Questionnaire and the Food Intake Assessment Preference Questionnaire
  • Individuals in the same age range who regularly use e-cigarettes (vape) can complete the Vaping Questionnaire and the Vaping Assessment Preference Questionnaire, in addition to the Demographics Questionnaire and the Food Intake Assessment Preference Questionnaire
  • Individuals in the same age range who regularly drink alcohol can complete the Alcohol Consumption Questionnaire and the Alcohol Consumption Assessment Preference Questionnaire, in addition to the Demographics Questionnaire and the Food Intake Assessment Preference Questionnaire

Individuals who engage in several of these behaviors can complete all questionnaires that apply.

Exclusion Criteria:

• Individuals who are unwilling to participate in this survey

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Online Survey
Individuals who are willing to participate in this online survey

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Demographic data
Time Frame: Day of survey completion, up to 12 months
age, sex, race/ethnicity, marital status, education, employment status, household income, zip code, height and weight, the prevalence of cardiovascular risk factors and cancer, and food security status
Day of survey completion, up to 12 months
Smoking behavior
Time Frame: Day of survey completion, up to 12 months
smoking status, history, frequency, amount, cues, motivation to quit, and potential factors affecting the decision to quit including the effect of smoking on food cravings
Day of survey completion, up to 12 months
Vaping behavior
Time Frame: Day of survey completion, up to 12 months
vaping status, history, frequency, amount, cues, motivation to quit and potential factors affecting the decision to quit including the effect of vaping on food cravings
Day of survey completion, up to 12 months
Alcohol consumption
Time Frame: Day of survey completion, up to 12 months
alcohol consumption status, history, frequency, amount, cues, motivation to quit/reduce consumption, and the effect of alcohol consumption on food cravings
Day of survey completion, up to 12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Smoking Assessment Preference
Time Frame: Day of survey completion, up to 12 months
This questionnaire assesses the willingness to use different methods to monitor smoking behavior such as a pen-and-paper record or a smartphone app
Day of survey completion, up to 12 months
Vaping Assessment Preference
Time Frame: Day of survey completion, up to 12 months
This questionnaire assesses the willingness to use different methods to monitor vaping behavior such as a pen-and-paper record or diary, a 24-hour recall, or a smartphone app
Day of survey completion, up to 12 months
Alcohol Consumption Assessment Preference
Time Frame: Day of survey completion, up to 12 months
This questionnaire assesses the willingness to use different methods to monitor alcohol consumption such as a pen-and-paper record or diary, a 24-hour recall, or smartphone app-based methods (remote photography or in-app self-estimation of drink sizes)
Day of survey completion, up to 12 months
Food Intake Assessment Preference Questionnaire
Time Frame: Day of survey completion, up to 12 months
This questionnaire assesses the willingness to use different methods to monitor food intake such as a pen-and-paper record or diary, a 24-hour recall, or smartphone app-based methods (remote food photography or in-app self-estimation of portion sizes)
Day of survey completion, up to 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Corby K Martin, PhD, Pennington Biomedical Research Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2020

Primary Completion (Actual)

November 6, 2020

Study Completion (Actual)

November 6, 2020

Study Registration Dates

First Submitted

October 28, 2019

First Submitted That Met QC Criteria

November 1, 2019

First Posted (Actual)

November 4, 2019

Study Record Updates

Last Update Posted (Actual)

April 19, 2021

Last Update Submitted That Met QC Criteria

April 15, 2021

Last Verified

April 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2019-052-PBRC

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Access to individual de-identified data is possible via Pennington Biomedical Research Center's Data Sharing policy.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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