Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

Personalized Intervention Program: Tobacco Treatment for Patients at Risk for Lung Cancer (PIP)

NCT02658032 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to test the efficacy of two separate, sequential interventions to promote tobacco cessation/reduction in patients who are screened for lung cancer or are eligible for lung cancer screening. Each intervention will be compared to standard of care. The first intervention will be a personalized message intervention, the second intervention will consist of a biofeedback-based intervention.

Interventions

  • OTHER standard care
  • BEHAVIORAL personalized cessation care
  • BEHAVIORAL bio feedback

Study Locations (2)

Connecticut

  • Yale University — New Haven

South Carolina

  • Medical University of South Carolina: Hollings Cancer Center — Charleston

Trial Details

FieldValue
Enrollment Target 276 participants
Start Date 2016-01
Est. Completion 2020-10
Phase NA

Sponsor

Yale University

1,283 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02658032

The ClinicalTrials.gov registry entry for NCT02658032 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 276 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,283 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 Smoking Cessation appearing as the primary indexed condition, and to 3 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: NCT02658032 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Connecticut, South Carolina. 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 NCT02658032 about?

NCT02658032 is a clinical study titled "Personalized Intervention Program: Tobacco Treatment for Patients at Risk for Lung Cancer (PIP)". The purpose of this study is to test the efficacy of two separate, sequential interventions to promote tobacco cessation/reduction in patients who are screened for lung cancer or are eligible for lung cancer screening. Each intervention will be compared to standard of care. The first intervention wi...

What is the current status of trial NCT02658032?

This trial is currently completed. It is a NA study. The enrollment target is 276 participants. The study started on 2016-01. Estimated completion is 2020-10.

What conditions does trial NCT02658032 study?

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

What interventions are being tested in trial NCT02658032?

The interventions under investigation include: standard care (OTHER), personalized cessation care (BEHAVIORAL), bio feedback (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02658032?

This trial is sponsored by Yale University, which has 1,283 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02658032 being conducted?

This trial has 2 study locations across Connecticut, South Carolina. 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