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Just Kwit: Mobile Intervention for Tobacco Cessation

University of Pittsburgh logo

University of Pittsburgh

Status

Completed

Conditions

Smoking Cessation

Treatments

Other: Kwit smartphone app

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03538678
K07CA222338 (U.S. NIH Grant/Contract)
PRO18010454

Details and patient eligibility

About

The intervention will be use of a smartphone app to support tobacco cessation. The app's main features include sending motivational messages, displaying money saved, and allowing the user to log cravings.

Full description

The investigators will recruit hospitalized young adult smokers aged 18-30 interested in cessation over a six-month period. Patients will all receive a UPMC Tobacco Treatment Service counseling session focused on motivational interviewing prior to participation in the study. Upon consent, participants will then be randomized 1:1 to either standard patient-initiated follow-up or use of the Kwit app. Participants will be stratified by sex because males and females are known to have highly variable responses to existing tobacco control interventions. Investigators will systematically assess feasibility using established Likert-type items factors such as interaction, features, engagement, trust, and impact.

If a participant consents to the study, they will be given a brief survey to collect general information related to their smoking behavior. After 30 days, a follow-up survey will be conducted to assess their current smoking behavior. Participants randomized to the experimental arm will be asked additional questions about their use of the smartphone app.

Enrollment

40 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18-30 smokers interested in cessation (>5 cigarettes/day over the past 30 days)
  • Must own an Apple or Android based smartphone.

Exclusion criteria

  • Already receiving pharmacological and/or behavioral intervention or counseling for smoking cessation.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Kwit app
Experimental group
Description:
Use of Kwit smartphone app
Treatment:
Other: Kwit smartphone app
Standard of care
No Intervention group
Description:
Patient initiated follow-up post discharge

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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