CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 154 enrolled
Drug / intervention
Puff Topography Biofeedback Training +1 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05644002
NCT05644002N/ACompleted

A Puff Topography Biofeedback Paradigm to Reduce Stress-Precipitated Smoking Reinforcement

Rutgers, The State University of New Jersey·interventional·Posted Dec 9, 2022·Updated Feb 24, 2025

In Brief

A clinical study evaluating Puff Topography Biofeedback Training and Control for Cigarette Smoking. Completed, enrolled 154 participants across 1 site.

Detailed Summary

The purpose of the study is to examine the effects of a novel bio-behavioral paradigm, entitled, Puff Topography Biofeedback Training, compared to a control condition, in reducing stress-induced smoking reinforcement.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2023202420252026
First PostedDec 9, 2022
Enrollment StartMar 21, 2022
Primary CompletionSep 13, 2023
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 3.6 years ago

Interventions

Puff Topography Biofeedback Trainingbehavioral

Visit 1: Participants will be asked to smoke their usual brand cigarette using the CReSS smoking topography device. Participants will be instructed on how to follow visual and auditory puffing prompts provided to them by a computer program in order to control puffing behavior for a duration of five minutes. Visit 2: Participants will be instructed to smoke their cigarette using the CReSS device and instructions provided during Visit 1 after undergoing a brief laboratory stress induction.

Controlbehavioral

Visit 1: Participants will be instructed to smoke their usual brand cigarette using the CReSS smoking topography device while passively viewing time-matched control stimulus presented to them on a computer monitor for a duration of five minutes. Visit 2: Participants will be instructed to smoke their cigarette using the CReSS device and instructions provided during Visit 1 after undergoing a brief laboratory stress induction.