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Evaluating the Feasibility and Efficacy of a Real-time Smoking Intervention Using Wearable Technology

NCT04172623 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2023-02-13

Study results available
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Summary

This study will use wearable technology to test the feasibility and efficacy of delivering a novel real-time smoking intervention to improve standard tobacco treatment.

Conditions

  • Tobacco Use Cessation

Interventions

BEHAVIORAL

Real-Time Smoking Intervention

Adult smokers will use wearable technology in order to receive real-time feedback as a smoking intervention in addition to standard treatment.

BEHAVIORAL

Standard Treatment

Adult smokers will receive standard outpatient tobacco treatment.

Sponsors & Collaborators

  • Patterson Trust Mentored Research Award: Clinical, Health Services and Policy Research

    collaborator OTHER

  • Yale University

    lead OTHER

Principal Investigators

  • Krysten Bold, Ph.D. · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-01
Primary Completion
2022-01-31
Completion
2022-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04172623 on ClinicalTrials.gov