Trauma-Informed Care for Smoking Cessation for Pregnancy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of California, San Francisco

About this trial

Trauma-informed approaches have been shown to support recovery from other substance use disorders and involve four key elements: (1) Realizing the prevalence of trauma and pathways to recovery, (2) Recognizing symptoms of trauma, (3) Responding by embedding knowledge of trauma into practices and policies and (4) Resisting re-traumatization (the 4Rs). In close partnership with Breathe California and a public safety-net clinic in San Francisco that serves primarily racial and ethnic minoritized (REM) pregnant women, the 4Rs along with the Ask, Advise, Assess, Assist and Arrange (the 5As) evidence-based intervention for tobacco cessation that is delivered by health care professionals and is a US Public Health Services clinical practice guideline for treating tobacco will be used to create and implement a smoking cessation intervention for pregnant women with experiences of trauma.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Nurse practitioner, physician assistant, nurse-midwife, medical doctor, registered nurse, clinical pharmacist, behavioral health professional, social worker, or any other healthcare professional caring for pregnant patient-participants.

Age ≥ 18 years old.

Currently smoking or report having smoked during a previous pregnancy

Age ≥18 years old.

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Expired carbon monoxide (CO)

    Other intervention

    Expired CO will be measured using a non-investigational device

  • Interviews

    Other intervention

    Participants will be interviewed via video conference or in person

  • Questionnaires

    Other intervention

    Participants will receive questionnaires to complete through the course of the study

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Aim 1: Development, Pilot GroupExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Number of themes (Aim 1)

Themes related to how to improve smoking cessation for pregnant people will be identified through in-depth interviews.

Time frame
Up to 6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of California, San Francisco

Lead sponsor

Tobacco Related Disease Research Program

Collaborator