Skip to content

App for Pregnancy Smoking Cessation With Peer Support

A Smartphone Intervention for Pregnancy Smoking Cessation With Peer Support

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05337722
Acronym
SFT
Enrollment
790
Registered
2022-04-20
Start date
2023-01-11
Completion date
2026-08-31
Last updated
2026-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking Cessation, Tobacco Smoking

Brief summary

The objectives of this project are to develop, implement, and test the feasibility and effectiveness of an artificial intelligence adaptive mobile pregnancy tobacco cessation app-based intervention using deep tailoring and a self-nominated support person, and to build mHealth research capacity in Romania. The central hypothesis is that the intervention will show evidence of feasibility and effectiveness in increasing positive support, pregnancy cessation, and postnatal abstinence. The intervention is grounded in Self-Determination Theory (SDT) and Motivational Interviewing (MI), a counselling style that is effective in assisting people to quit smoking. The app will be novel in its use of the unique functionality of smartphones, use of reinforcement learning (RL) and deep tailoring to continuously adapt the intervention, the emphasis on increasing positive support, and the use of the app by both smoker and support person. The long-term goal of the research program is to use mHealth for smoking cessation leveraging the unique functionality of smartphones and to continue building mHealth research capacity and developing research networks in Central and Eastern Europe (CEE) and other LMICs. Aim 1 (R21 phase). Develop and test the feasibility and acceptability of the SFT2.0 app-based mobile smoking cessation intervention with a support person during pregnancy and postpartum in Romania. Through a user-centered and iterative design the investigators will enhance the SFT1.0 app, deepen the tailoring, incorporate RL, expand the app for use by any support person, and test the intervention including the app and MI video counseling in a series of usability studies and a 12-week open trial (n=20). Aim 2 (R33 phase). Test the SFT2.0 app-based smoking cessation intervention in a hybrid effectiveness and implementation randomized controlled trial. The investigators will randomize 375 pregnant smokers and their support persons to i) a fixed arm, including the SFT2.0 app for both, and fixed pre- and postnatal MI counseling; ii) an RL-adaptive arm, with the app continuously optimizing as-needed MI counseling; or iii) control group. Aim 3 (R21 and R33 phases). Develop mHealth research capacity by enhancing individual and institutional research capabilities in Romania and expanding the existing international research network.

Interventions

BEHAVIORALSFT 2.0

The SFT 2.0 intervention will include the use of the SFT 2.0 smoking cessation app, Motivational Interviewing (MI) counseling, and the support of a peer person

BEHAVIORALActive control

Low dose prenatal and postnatal MI video counseling, defined as one prenatal session and one postnatal session

Sponsors

Michigan State University
Lead SponsorOTHER
Babes-Bolyai University
CollaboratorOTHER
Wake Forest University Health Sciences
CollaboratorOTHER
University of Michigan
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* age\>=18 * pregnant * user of regular cigarettes * availability of Android phone with broadband data

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Change in smoking cessation3 and 6 months after birth7-day point biochemically verified prevalence of tobacco use
Change in postpartum abstinence3 and 6 months after birthFewer than 5 cigarettes smoked since birth
Reach1 month after birthProportion and representativeness (e.g., age, ethnicity) of dyads who enroll in each trial arm compared to each other and the general population of pregnant women in Romania
Adoption1 month after birthProportion of participants who enroll in SFT2.0 by recruitment strategy
Implementation1 month after birthParticipants frequency of overall SFT2.0 use and of the different app components
User engagement1 month after birthquality of the user experience when interacting with SFT2.0 measured using the four constructs of the User Engagement Scale short form: focused attention (e.g., The time I spent using SFT just slipped away), perceived usability (e.g., I was frustrated while using SFT), aesthetic appeal (e.g., SFT was attractive), and rewarding (e.g., Using SFT was worthwhile). Each construct includes 3 items (score 3-15) and can be treated as subscales or as a summary score of user engagement (4-60). An overall engagement score can be calculated by adding all of the items together and dividing by twelve. Higher scores mean a better outcome.

Countries

Romania

Contacts

CONTACTCristian I Meghea, PhD
meghea@msu.edu2487161043
CONTACTOana M Blaga
oana.blaga@ubbcluj.ro+40 749240017

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026