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Text-Messaging Intervention for Quitting E-Cigarettes

N/A
Recruiting
Research Sponsored by Seok Hyun Gwon
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up throughout 12 months
Awards & highlights

Study Summary

This trial tests if text messages can help young adults in rural areas quit smoking e-cigarettes.

Who is the study for?
This trial is for English-speaking young adults aged 18-24 who use e-cigarettes every day, own a mobile phone with texting and internet, know how to text, plan to quit vaping soon, and live in rural areas of Wisconsin, Minnesota, North Dakota or South Dakota.Check my eligibility
What is being tested?
The study is testing a new text-messaging program designed to help people stop using e-cigarettes. Participants will either receive standard care resources or the special text-message intervention. The trial aims to see if this method is workable and liked by users.See study design
What are the potential side effects?
Since this trial involves a text-messaging intervention for quitting e-cigarettes rather than medication or medical procedures, there are no direct physical side effects expected from participating.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~throughout 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and throughout 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Concentration of cotinine in saliva
Level of acceptability of the intervention
Nicotine dependence (Penn State Electronic Cigarette Dependence Index)
+5 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention (E-cigarette cessation text-messaging intervention)Experimental Treatment1 Intervention
Group II: Standard care (Standard care control using standard national resources)Active Control1 Intervention
This standard care group will receive standard care resources from smokefree.gov.

Find a Location

Who is running the clinical trial?

Seok Hyun GwonLead Sponsor

Media Library

E-cigarette cessation text-messaging intervention Clinical Trial Eligibility Overview. Trial Name: NCT05906082 — N/A
E-Cigarette Use Research Study Groups: Standard care (Standard care control using standard national resources), Intervention (E-cigarette cessation text-messaging intervention)
E-Cigarette Use Clinical Trial 2023: E-cigarette cessation text-messaging intervention Highlights & Side Effects. Trial Name: NCT05906082 — N/A
E-cigarette cessation text-messaging intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT05906082 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any restrictions on who may enroll in this clinical research?

"This medical trial is seeking out 50 volunteers that are between 18 and 24 years old that have a history of e-cigarette use."

Answered by AI

Is there an age constraint for enrollment in this research endeavor?

"This medical trial is restricted to those aged between 18 and 24 years old. However, there are 4 other trials open for individuals either below the age of consent or above 65."

Answered by AI

What is the aggregate number of participants included in this clinical experiment?

"Affirmative. The information hosted on clinicaltrials.gov conveys that this experimental trial is now recruiting participants. This study was originally posted on May 25th 2023 and subsequently amended on June 6th 2023 with the need for 50 individuals at 1 facility."

Answered by AI

Are there still opportunities for prospective participants in this clinical trial?

"Affirmative. According to clinicaltrials.gov, this investigation was first made available on May 25th 2023 and is still actively seeking enrollees as of June 6th 2023. The necessary number of participants needed amounts to 50 individuals from a single medical centre."

Answered by AI
~21 spots leftby Dec 2024