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Re-Connect Application for Smoking Cessation

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Rowan University

Status

Enrolling

Conditions

Nicotine Dependence, Cigarettes
Acceptability of Health Care
Smoking Cessation

Treatments

Behavioral: Abstinent Contingent (AC) Re-Connect
Behavioral: Submission Contingent (SC) Re-Connect

Study type

Interventional

Funder types

Other

Identifiers

NCT05224154
PRO-2020-123

Details and patient eligibility

About

This series of studies will explore the acceptability, feasibility, and preliminary efficacy of making access to smartphone applications contingent on objective evidence of smoking abstinence.

Full description

Aim 1 will use small focus groups and feedback sessions (n = 4-6) to gain insight into the acceptability and usability of Re-Connect. Up to 3 single-case design studies (n = 4/round) will then be conducted to get more extended use of the app in a real world context to get additional information about usability and acceptability of the app. Aim 2 will involve a 2-group (AC vs SC), pilot randomized control trial to test the feasibility, acceptability, and preliminary efficacy of Re-Connect.

Enrollment

82 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • individuals who report smoking at least 10 cigarettes per day for at least 2 years, -18 years of age or older
  • do not have any health complications that might interfere with the study or require more intensive treatment (e.g., emphysema, chronic obstructive pulmonary disorder, asthma, lactose intolerance)
  • report a strong desire to quit smoking (8 or higher on a 10-point Likert scale)
  • has prior experience using a smartphone, speak English, and are literate, will be eligible for the study.

Exclusion criteria

  • Individuals with mental health complications that are either un-managed or that have been managed for less than 6-months

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

82 participants in 2 patient groups

Abstinent Contingent (AC) Re-Connect
Experimental group
Description:
Participants in this group will be able to unblock highly desired, but non-essential (e.g., social networking, shopping, games) applications contingent on meeting goals for smoking abstinence, as verified by meeting carbon monoxide goals (CO\<=6ppm).
Treatment:
Behavioral: Abstinent Contingent (AC) Re-Connect
Submission Contingent (SC) Re-Connect
Active Comparator group
Description:
Participants in this group will also be able to unblock their applications, but contingent on submitting CO samples and independent of meeting CO goals for smoking abstinence.
Treatment:
Behavioral: Submission Contingent (SC) Re-Connect

Trial contacts and locations

1

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Central trial contact

Bethany Raiff, PhD

Data sourced from clinicaltrials.gov

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