A Behavioral Activation Prenatal and Postpartum Intervention for Depressed Pregnant Smokers
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT05044546
- Status
- Active Not Recruiting
Conditions
- Depression
- Tobacco Use Disorder
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Behavioral Activation Therapy — BEHAVIORALParticipate in BA counseling
- Discussion — PROCEDUREParticipate in focus group
- Health Education — BEHAVIORALParticipate in health and wellness education counseling
- Questionnaire Administration — OTHERAncillary studies
- Tobacco Cessation Counseling — OTHERParticipate in smoking cessation counseling
Study Details
This study evaluates a mood management and health and wellness smoking cessation intervention for depressed pregnant smokers during and after birth. This study may help pregnant smokers who are experiencing depression quit smoking and stay smoke-free after their babies are born.
Key Dates
- Start date
- Oct 19, 2021
- Status verified
- Jan 2026
- Primary completion
- Nov 22, 2024
- Completion
- Jan 31, 2027
Study Design
- Enrollment
- 26 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- PREVENTION
Arms
- Experimental: Aim 1 and secondary aim 2 (focus group)Participants participate in focus group over 60-90 minutes. Participants who completed and dropped out of postpartum treatment also participate in a focus group.
- Experimental: Aim 3 Group I (BA)Participants participate in smoking cessation counseling over 15 minutes and BA counseling sessions over 45 minutes once a week for 10 weeks to pilot test delivery via smart phone videoconferencing and to conduct process evaluation of technical issues in use of smart phones.
- Experimental: Aim 3 Group II (HW)Participants participate in smoking cessation counseling over 15 minutes and health and wellness education counseling sessions over 45 minutes once a week for 10 weeks to pilot test delivery via smart phone videoconferencing and to conduct process evaluation of technical issues in use of smart phones.
- Experimental: Aim 4 Group III (BA)During the prenatal period, participants of 18-22 weeks gestational age will receive 10 individual sessions with 15 minutes of smoking cessation counseling ad 45 minutes of behavioral activation counseling sessions. These women will have 16 weeks to complete their 10 individual sessions.
- Experimental: Aim 4 Group IV (HW)During the prenatal period, participants of 18-22 weeks gestational age will receive 10 individual sessions with 15 minutes of smoking cessation counseling and 45 minutes of health and wellness education counseling sessions. These women will have 16 weeks to complete their 10 individual sessions.
Primary Outcome Measure
Abstinence [ Time Frame: Last treatment visit at 10 weeks or earlier if participant was lost to follow up ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| M D Anderson Cancer Center | Houston | Texas | 77030 | - |
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