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

NCT01625767 · ClinicalTrials.gov registry record · Phase 2

Tobacco Approach Avoidance Training for Adolescent Smokers-1

A Phase 2 study of Tobacco Use Disorder, sponsored by Yale University.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target
1
Study location

NCT01625767: Completed Phase 2 study of Tobacco Use Disorder, sponsored by Yale University.

NCT01625767 is a Phase 2 study of Tobacco Use Disorder that has completed, run by Yale University. The registered enrollment target is 40 participants, below the 239-participant average among 70 other Tobacco Use Disorder trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01625767, a Phase 2 study of Tobacco Use Disorder, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

This is a two part study. Study 1 will compare Approach Avoidance Training (AAT) responses in smokers and nonsmokers in order to confirm that adolescent smokers experience cognitive bias towards tobacco-related stimuli.

Primary Outcome

For all AAT comparisons, the investigators will compare median scores (to minimize influence of outliers) for cigarette approach and cigarette avoid RTs. The difference between these values gives the smoking AAT-scores, which the investigators expect to not differ from zero in the non-smokers (or to show mild avoidance), while it is expect that smokers will be faster to approach than to avoid cigarettes. ANOVA models will be used to compare scores in smokers vs. nonsmokers. Regression analyses w

Conditions Studied

Interventions

  • BEHAVIORAL AAT experiment

Study Locations (1)

Connecticut

  • Yale University, School of Medicine, Dpeartment of Psychiatry - New Haven

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2011-09
Est. Completion 2012-03
Phase Phase 2
Yale University

1,492 total trials

What the finished NCT01625767 record still lists

NCT01625767 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 239-participant average among 70 other Tobacco Use Disorder trials with a reported enrollment target (83% lower).

The record links to 1 condition, with Tobacco Use Disorder appearing as the primary indexed condition, and to 1 intervention - of which AAT experiment is the first listed.

NCT01625767 reports a single indexed study location in Connecticut.

Frequently Asked Questions

What is clinical trial NCT01625767 about?

NCT01625767 is a clinical study titled "Tobacco Approach Avoidance Training for Adolescent Smokers-1". This is a two part study. Study 1 will compare Approach Avoidance Training (AAT) responses in smokers and nonsmokers in order to confirm that adolescent smokers experience cognitive bias towards tobacco-related stimuli.

What is the current status of trial NCT01625767?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2011-09. Estimated completion is 2012-03.

What conditions does trial NCT01625767 study?

This clinical trial studies the following conditions: Tobacco Use Disorder.

What interventions are being tested in trial NCT01625767?

The interventions under investigation include: AAT experiment (BEHAVIORAL).

Who is sponsoring clinical trial NCT01625767?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01625767 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Tobacco Use Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01625767's enrollment target sits among peer trials

40 59th of 70 higher than 12 of 70 other Tobacco Use Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Tobacco Use Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01625767, the US trial registry maintained by the National Library of Medicine. NCT01625767 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.