Helping low-income pregnant women in Northeast Texas quit smoking
Official title: Increasing Access to Smoking Cessation and Smoke Free Home Services for Low-Income Pregnant Women in Northeast Texas
Run by M.D. Anderson Cancer Center · NCT05051345 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing a program to help low-income pregnant women in Northeast Texas quit smoking by providing them with counseling, a wellness app, and resources for creating smoke-free homes.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 54158 (estimated) |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT05051345 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are low-income pregnant women residing in Texas who are current smokers or have recently quit smoking.
✕Probably not a fit
Patients who are not currently pregnant or do not reside in Texas may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This trial aims to enhance access to smoking cessation services for low-income pregnant women in Northeast Texas. It focuses on proactive referrals to evidence-based counseling, app-based smoking cessation support, and smoke-free home interventions. Participants will engage in telephone counseling sessions during pregnancy and postpartum, utilize a wellness app for resources, and receive materials to promote smoke-free environments. The overall goal is to support healthier choices for mothers and their infants.
Why it matters
Potential benefit: If successful, this initiative could significantly reduce smoking rates among pregnant women, leading to healthier pregnancies and improved infant outcomes.
How similar studies have gone: Other studies have shown success in similar smoking cessation interventions for pregnant women, indicating a promising approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * PRE-TEST SURVEY FOR PREGNANT WOMEN: Currently pregnant * PRE-TEST SURVEY FOR PREGNANT WOMEN: Currently receiving services at one of the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) or Federally Qualified Health Centers (FQHC) clinics listed in the protocol * PRE-TEST SURVEY FOR PREGNANT WOMEN: Self-report being a current smoker, having quit for the pregnancy or allowing smoking in the home * PRE-TEST SURVEY FOR PREGNANT WOMEN: Reside in Texas * PRE-TEST SURVEY FOR PREGNANT WOMEN: Consent to take surveys * PRE-TEST SURVEY FOR PREGNANT WOMEN: English or Spanish speaking * SERVICES OFFERED TO PREGNANT WOMEN: Currently pregnant or within the first 4 months of postpartum period * SERVICES OFFERED TO PREGNANT WOMEN: Self-report that they are currently receiving services at one of the WIC or FQHC clinics listed in the protocol * SERVICES OFFERED TO PREGNANT WOMEN: Self-report being a current smoker, having quit for the pregnancy or allowing smoking in the home * SERVICES OFFERED TO PREGNANT WOMEN: Reside in Texas * SERVICES OFFERED TO PREGNANT WOMEN: Willing to provide address, telephone contact or download app onto their smartphones * SERVICES OFFERED TO PREGNANT WOMEN: English or Spanish speaking * HOUSEHOLD MEMBERS OF PREGNANT WOMEN: Self-report that he/she currently smokes and lives in the household with the pregnant woman who is receiving services * HOUSEHOLD MEMBERS OF PREGNANT WOMEN: Reside in Texas * HOUSEHOLD MEMBERS OF PREGNANT WOMEN: English or Spanish speaking * SERVICES OFFERED TO NON-PREGNANT INDIVIDUALS: Currently receiving services at one of the WIC or FQHC clinics listed in the protocol * SERVICES OFFERED TO NON-PREGNANT INDIVIDUALS: Self-report being a current smoker or allowing smoking in the home * SERVICES OFFERED TO NON-PREGNANT INDIVIDUALS: Reside in Texas * SERVICES OFFERED TO NON-PREGNANT INDIVIDUALS: English or Spanish speaking
Where it's running
-
M D Anderson Cancer Center
Houston, Texas, United States Recruiting
Study contacts
- Principal investigator: Jan Blalock — M.D. Anderson Cancer Center
- Study coordinator: Jan Blalock
- Email: jablaloc@mdanderson.org
- Phone: 713-745-1728
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.