Feasibility and Acceptability Trial to Reduce Tobacco and Cannabis Use During Pregnancy and Postpartum
This study is testing a behavioral intervention to help pregnant individuals stop using tobacco and cannabis, and to stay quit after giving birth. The intervention involves one-on-one sessions with a study interventionist, focusing on education and discussion about self-monitoring and problem-solving. You may be able to join if you are pregnant, under 26 weeks gestation, plan to remain pregnant, speak English, and use tobacco and/or cannabis. The study aims to see how well people attend and complete these sessions, and if they find the intervention helpful. The current status of this study is unclear, and it plans to enroll 25 participants.
- Study design
- This is an interventional study with an unclear status, planning to enroll 25 participants.
- What's involved
- You would meet one-on-one with a study interventionist for 6 sessions during pregnancy and 3 sessions after birth.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will track your attendance, completion of procedures, and how acceptable you find the intervention from enrollment until 3 months postpartum.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Feasibility and Acceptability Trial to Reduce Tobacco and Cannabis Use During Pregnancy and Postpartum
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Natacha De Genna · PRINCIPAL_INVESTIGATOR · University of Pittsburgh
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- AttendanceFrom enrollment to 3 months postpartum
Rate of attendance will be measured by proportion of sessions attended to total available sessions.
- Completion of Intervention-Related ProceduresFrom enrollment to 3 months postpartum
Participant will complete activities designed to help them self-monitor their smoking-related behaviors during and between scheduled treatment sessions. Completion of activities will be measured by the proportion of completed activities to the total number of assigned activities.
- Acceptability of the InterventionFrom enrollment to 3 months postpartum
Participants' acceptance of the intervention will be measured using the Acceptability of Intervention Measure (AIM) at the 3-month postpartum assessment. This is a 4-item questionnaire with a scale range of 4-20, with a higher score indicating greater acceptance.