- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02144883
Telephone Counseling for Pregnant Smokers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Smoking during pregnancy increases the risk of low birth weight, premature delivery, fetal and infant death, and children's developmental problems. It is also associated with significant economic costs. Telephone cessation quitlines have been suggested as one good way to reach pregnant smokers.
This randomized controlled trial was embedded into a free statewide telephone cessation quitline in California. The primary component of the intervention was telephone counseling using a structured protocol developed specifically for the pregnant population. The counseling consisted of nine counseling sessions.
A secondary component of the intervention was the mailed materials. Following enrollment in the study all subjects (control and intervention) received a self-help quit kit for pregnant smokers and fact sheets on second-hand smoke and additional tips for quitting while pregnant. Subjects in the counseling intervention group received five additional mailings. These mailings were designed to remind them of their commitment to quitting and of the presence of counseling support if they needed help.
Prior to 36 weeks gestation (in the third trimester), 2-months postpartum, and 6-months postpartum we conducted a brief telephone survey to assess smoking status. The information obtained allowed us to determine 30-day prolonged abstinence rates.
Prior to 36 weeks gestation (in the third trimester), the investigators sent a kit and requested saliva samples be mailed back to biochemically verify smoking status by testing for cotinine and nicotine byproducts.
Study Type
Enrollment (Actual)
Phase
- Phase 3
Contacts and Locations
Study Locations
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California
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San Diego, California, United States, 92111
- University of California San Diego California Smokers' Helpline
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Current smoker willing to quit within one month
- Recent quitters
- First time quitline caller
- Less than 27 weeks gestation
- English and/or Spanish speaking
- Valid phone number
- Valid address
- Gave consent to participate in study and evaluation
Exclusion Criteria:
- Active psychiatric disorder
- Substance or alcohol abuse
- Had been in recovery from alcohol or other substances for less than 6 months
- Planned to use pharmacotherapy
- Insufficient contact information
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Materials
Self-help materials mailed to subjects home.
|
All subjects received a self-help quit kit for pregnant smokers and fact sheets on second-hand smoke and additional tips for quitting while pregnant.
Subjects in the counseling intervention group received five additional mailings.
These mailings were designed to remind them of their commitment to quitting and of the presence of counseling support if they needed help.
Mailings included a pamphlet on pregnancy facts, a refrigerator magnet with the quitline number, and a social support planning worksheet that were sent at 4.5 months, 6 months, and 7.5 months gestation, respectively.
They also received a congratulatory card soon after the birth and a brochure with tips for parenting newborns that was sent at one month postpartum.
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Experimental: Telephone Counseling and Materials
Subjects received up to 9 telephone counseling calls plus self-help quit kit and 5 additional mailings
|
All subjects received a self-help quit kit for pregnant smokers and fact sheets on second-hand smoke and additional tips for quitting while pregnant.
Subjects in the counseling intervention group received five additional mailings.
These mailings were designed to remind them of their commitment to quitting and of the presence of counseling support if they needed help.
Mailings included a pamphlet on pregnancy facts, a refrigerator magnet with the quitline number, and a social support planning worksheet that were sent at 4.5 months, 6 months, and 7.5 months gestation, respectively.
They also received a congratulatory card soon after the birth and a brochure with tips for parenting newborns that was sent at one month postpartum.
Subjects randomized into the telephone counseling condition received one comprehensive pre-quit call lasting about 45 minutes; five follow-up calls during the pregnancy, scheduled according to the risk of relapse after the quit attempt (1, 3, 7, 14, and 30 days after the quit date) one 30-minute pre-birth call scheduled after 36 weeks gestation and two additional follow-up sessions scheduled for 14 and 28 days after the baby's birth.
The counseling used a proactive calling procedure in that counselors made all the calls based on agreed-upon dates with the clients.
This proactive approach aimed to foster a positive counseling relationship, provide accountability, and create opportunities to address wavering motivation, reduce attrition, and minimize relapse.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
30 days prolonged abstinence
Time Frame: 6-months postpartum
|
Conducted a brief telephone survey to assess smoking status.
The information obtained allowed us to determine 30-day prolonged abstinence rates.
|
6-months postpartum
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of smokers making a 24-hour quit attempt
Time Frame: <36 weeks gestation
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During evaluation call subjects were asked if they had made a quit attempt that lasted at least 24 hours.
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<36 weeks gestation
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Relapse curve based on quit attempt
Time Frame: Seven months post enrollment
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Kaplan-Meier analysis on the quit attempts over a 6 month period.
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Seven months post enrollment
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Percentage of smokers making a 24-hour quit attempt
Time Frame: 2-months postpartum
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During evaluation call subjects were asked if they had made a quit attempt that lasted at least 24 hours.
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2-months postpartum
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Percentage of smokers making a 24-hour quit attempt
Time Frame: 6-months postpartum
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During evaluation call subjects were asked if they had made a quit attempt that lasted at least 24 hours.
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6-months postpartum
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7-day cotinine verified abstinence
Time Frame: <36 weeks gestation
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Subjects were asked to submit a saliva sample.
This sample was sent to a laboratory to test the cotinine level.
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<36 weeks gestation
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30 days prolonged abstinence
Time Frame: <36 weeks gestation
|
Conducted a brief telephone survey to assess smoking status. The information obtained allowed us to determine 30-day prolonged abstinence rates. Safety Issue? (FDAAA) No |
<36 weeks gestation
|
|
30 days prolonged abstinence
Time Frame: 2-months postpartum
|
Conducted a brief telephone survey to assess smoking status. The information obtained allowed us to determine 30-day prolonged abstinence rates. Safety Issue? (FDAAA) No |
2-months postpartum
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Collaborators and Investigators
Collaborators
Publications and helpful links
General Publications
- Cummins, S.E., Tedeschi, G.J., Anderson, C.M., Quinlan-Downs, R., Harris, P., Zhu, S.-H. (2007). Telephone counseling for pregnant smokers: essential elements. Journal of Smoking Cessation, 2(2), 36-46.
- Cummins SE, Tedeschi GJ, Anderson CM, Zhu SH. Telephone Intervention for Pregnant Smokers: A Randomized Controlled Trial. Am J Prev Med. 2016 Sep;51(3):318-26. doi: 10.1016/j.amepre.2016.02.022. Epub 2016 Apr 4.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB #030310
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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