Actively Recruiting
Trauma-Informed Care for Smoking Cessation for Pregnancy
Led by University of California, San Francisco · Updated on 2026-04-23
20
Participants Needed
1
Research Sites
36 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
T
Tobacco Related Disease Research Program
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Trauma-Informed Care for Smoking Cessation for Pregnancy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinicians who are nurse practitioners, physician assistants, nurse-midwives, medical doctors, registered nurses, clinical pharmacists, behavioral health professionals, social workers, or other healthcare professionals caring for pregnant patients
- Age 18 years or older
- Pregnant women who currently smoke or have smoked during a previous pregnancy
- Pregnant women aged 18 years or older
- Identify as a cisgender woman or female at birth
- Have experienced trauma as defined by the DSM-5 traumatic exposure criteria
- Proficient in English or Spanish
- Current or former patients at participating clinical sites (for Aim 2 feedback participants)
- For Aim 3: Pregnant women actively smoking with a history of trauma, smoking at least 1 cigarette per day verified by carbon monoxide level of 6 ppm or higher
You will not qualify if you...
- Any condition, including active mental health crises or cognitive impairment, that would interfere with the ability to provide informed consent or safely complete the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Zuckerberg San Francisco General Hospital
San Francisco, California, United States, 94115
Actively Recruiting
Research Team
G
Gaby Luna-Victoria, MD, MAS
CONTACT
A
Anita Hargrave-Bouagnon
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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