Skip to main content
OpenTrials
Completed

NCT Number: NCT03038542

Quit4hlth: Enhancing Tobacco and Cancer Control Through Framed Text Messages

This study evaluates a text messaging intervention through a smokers' quitline. Smokers will either receive 30 weeks of tailored, gain-framed text messages or 30 weeks of tailored, standard care text messages, both combined with standard quitline treatment. We hypothesize that the gain-framed text message intervention will increase cessation rates at 30 weeks as compared to standard care text messages.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1) call the Quitline requesting assistance with quitting smoking, 2) be 18+ years old, 3) speak English, 4) have a verified New York address, and 5) opt into the standard Quitline texting protocol.

Exclusion criteria

-

Treatment and study plan

Gain-framed text messages

Behavioral

Standard care text messages

Behavioral

Primary outcomes

  1. survey of smoking status

    Time frame: Week 30

    smoking or abstinent

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Collaborators

  • Roswell Park Cancer Institute

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jan 31, 2017
Registry last updated
Jul 17, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.