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COMPLETED NA

Phone-Based Postpartum Continuing Care for Smoking Cessation

NCT01684592 · View on ClinicalTrials.gov ↗

Study Summary

Smoking is a leading cause of death and other negative health outcomes. While a high percentage of women quit smoking during pregnancy, the majority relapse in the first 6 months postpartum. We propose developing and pilot testing a phone-based postpartum continuing care (PPCC) protocol based on existing evidence-based approaches to increase smoking cessation, reduce relapse, increase early re-intervention, and reduce infant exposure to environmental tobacco smoke in the postpartum period.

Interventions

  • BEHAVIORAL Standard care
  • BEHAVIORAL Phone-based postpartum continuing care

Study Locations (2)

Illinois

  • Chestnut Global Partners — Bloomington

Maryland

  • Maryland Women's Center — Baltimore

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2012-10
Est. Completion 2015-03
Phase NA

Sponsor

Battelle Memorial Institute

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01684592

The ClinicalTrials.gov registry entry for NCT01684592 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Battelle Memorial Institute, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 2 interventions — of which Standard care is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01684592 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Illinois, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01684592 about?

NCT01684592 is a clinical study titled "Phone-Based Postpartum Continuing Care for Smoking Cessation". Smoking is a leading cause of death and other negative health outcomes. While a high percentage of women quit smoking during pregnancy, the majority relapse in the first 6 months postpartum. We propose developing and pilot testing a phone-based postpartum continuing care (PPCC) protocol based on exi...

What is the current status of trial NCT01684592?

This trial is currently completed. It is a NA study. The enrollment target is 130 participants. The study started on 2012-10. Estimated completion is 2015-03.

What conditions does trial NCT01684592 study?

This clinical trial studies the following conditions: Pregnancy, Smoking Cessation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01684592?

The interventions under investigation include: Standard care (BEHAVIORAL), Phone-based postpartum continuing care (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01684592?

This trial is sponsored by Battelle Memorial Institute, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01684592 being conducted?

This trial has 2 study locations across Illinois, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial