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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05906082
Other study ID # 23.179
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 25, 2023
Est. completion date December 31, 2024

Study information

Verified date February 2024
Source University of Wisconsin, Milwaukee
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a small pilot randomized controlled trial to evaluate the feasibility, acceptability, and preliminary efficacy of the e-cigarette cessation text-messaging intervention with young adults in rural areas.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 24 Years
Eligibility Inclusion Criteria: - English speaking - 18-24 years - everyday e-cigarette use in the past month - ownership of a mobile phone or smartphone with texting and internet access abilities - knowledge of how to use text messages - plan on quitting e-cigarette use within one month - home address in a rural county of Wisconsin, Minnesota, North Dakota, and South Dakota Exclusion Criteria: - Individuals who reported use of other tobacco products (e.g., cigarettes, smokeless tobacco) than e-cigarettes in the past month

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
E-cigarette cessation text-messaging intervention
This is the intervention for e-cigarette cessation using text messages targeting young adults in rural areas.
Standard care control using standard national resources
This is the standard care with national resources from smokefree.gov.

Locations

Country Name City State
United States University of Wisconsin-Milwaukee Milwaukee Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
Seok Hyun Gwon

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants recruited and randomized Number of participants recruited and randomized Throughout 12 months
Primary Self-reported proportion of text messages read Proportion of text messages read during the intervention or standard care at 1 month At 1 month
Primary Retention rates (proportion of participants remained until 1 month post-intervention from enrollment) Proportion of participants from enrollment to 1 month post-intervention or standard-care At 1 month
Primary Level of acceptability of the intervention When you had received our text messages from our VapeFreeTXT program 1 month ago, how many of our text messages did you read on a typical day? Not at all (1) Read about 25% messages (2) Read about half messages (3) Read about 75% messages (4) Read the entire messages (5)
How useful was our VapeFreeTXT program in helping you quit vaping? Not at all useful (1) Slightly useful (2) Moderately useful (3) Very useful (4) Extremely useful (5)
Did our VapeFreeTXT program make you think about quitting vaping? Not at all (1) Probably not (2) Neither yes nor no (3) Probably yes (4) Definitely yes (5)
Do you think our VapeFreeTXT program will change your vaping? Not at all (1) Probably not (2) Neither yes nor no (3) Probably yes (4) Definitely yes (5)
Would you recommend this program to a friend or others? Not at all (1) Probably not (2) Neither yes nor no (3) Probably yes (4) Definitely yes (5)
At 1 month
Primary Proportion of salivary cotinine samples returned Proportion of salivary cotinine samples returned to the office lab for cotinine analysis At 1 month
Primary Self-reported 7-days point prevalence abstinence from ENDS and other tobacco Self-reported 7-days point prevalence abstinence from ENDS and other tobacco At 1 month
Primary Concentration of cotinine in saliva Biochemically verified abstinence evaluated by salivary cotinine samples At 1 month
Primary Nicotine dependence (Penn State Electronic Cigarette Dependence Index) Nicotine dependence (minimum 0 to maximum 20, higher scores mean a worse outcome.) At 1 month
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