NCT07210567

Brief Summary

The purpose of the study is to develop a new quit-smoking treatment among individuals with a cancer diagnosis using a smartphone app.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
33mo left

Started Jan 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress9%
Jan 2026Dec 2028

First Submitted

Initial submission to the registry

September 17, 2025

Completed
20 days until next milestone

First Posted

Study publicly available on registry

October 7, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

January 6, 2026

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2028

Last Updated

January 7, 2026

Status Verified

January 1, 2026

Enrollment Period

2 years

First QC Date

September 17, 2025

Last Update Submit

January 6, 2026

Conditions

Keywords

quit smokingcancer survivors

Outcome Measures

Primary Outcomes (3)

  • System Usablity Scale

    Perceived usability and learnability of the app will be measured on a 5-point scale (1=strongly disagree; 5=strongly agree).

    End of Treatment at 4 Weeks

  • Client Satisfaction Questionnaire

    Perceived satisfaction with the treatment will be assessed on a 4-point scale (1=very dissatisfied; 4=very satisfied).

    End of Treatment at 4 Weeks

  • Percentage of Participants That Completed Questionnaires

    Completion of follow-up assessment will be calculated.

    3-month follow-up

Study Arms (2)

Mindfulness

EXPERIMENTAL

Participants will receive brief counseling, nicotine replacement therapy, and intervention content delivered via the app.

Behavioral: Mindfulness

Quitline

ACTIVE COMPARATOR

Participants will be referred to Quitline to receive standard care for smoking cessation.

Behavioral: Quitline

Interventions

MindfulnessBEHAVIORAL

Participants will complete 4 counseling sessions (30 minutes), download and use a smartphone app for 4 weeks, complete 4 online surveys (baseline, quit date, end of treatment, and 3-month follow-up), and a brief phone call at the end of treatment to provide feedback. Participants will use the app every day to complete daily diaries and ecological momentary assessments (EMAs), receive brief mindful skills, and practice formal mindfulness meditations (5-30 minutes). Participants will also be provided with nicotine patches.

Mindfulness
QuitlineBEHAVIORAL

Participants will be referred to Quitline to receive standard care smoking cessation treatment, including counseling and nicotine patches. Participants will complete 4 online surveys (baseline, quit date, end of treatment, and 3-month follow-up) and a brief phone call at the end of treatment to provide feedback. Participants will use the app every day to complete daily diaries.

Quitline

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • ≥18 years old
  • smoked ≥1 cigarette per day (even one or two puffs) within the past 30 days
  • having been diagnosed with cancer
  • being motivated to quit in the next 30 days
  • having a valid home address and functioning phone number
  • being able to read, write, and speak English
  • having a smartphone that allows installation of the app
  • willingness to download the app

You may not qualify if:

  • being enrolled in a smoking cessation program
  • current use of smoking cessation medications
  • evidence of current psychosis
  • current/planning pregnancy or lactation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Institute for Nicotine & Tobacco Studies

New Brunswick, New Jersey, 08901, United States

RECRUITING

MeSH Terms

Conditions

Smoking Cessation

Interventions

Mindfulness

Condition Hierarchy (Ancestors)

Health BehaviorBehavior

Intervention Hierarchy (Ancestors)

Cognitive Behavioral TherapyBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Min-Jeong Yang, PhD

    Rutgers, The State University of New Jersey

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Rutgers IRB/Human Research Protection Program

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

September 17, 2025

First Posted

October 7, 2025

Study Start

January 6, 2026

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2028

Last Updated

January 7, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations