CClinicalTrials.gg
WithdrawnNCT06386432Updated Oct 8, 2025

EQQUAL-NM for the Promotion of Smoking Cessation in Sexual and Gender Minority Young Adults in New Mexico

An interventional study of Smartphone App-delivered Smoking Cessation Intervention and Smartphone App-delivered Smoking Cessation Intervention in Cigarette Smoking-Related Carcinoma, sponsored by Fred Hutchinson Cancer Center. Withdrawn at 1 site in United States. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-10-08.

Sponsored by Fred Hutchinson Cancer Center · Not applicable, Interventional, and Prevention

Why this study was withdrawn
Study never opened to accrual and will not proceed due to lack of funding.
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

This clinical trial assesses the acceptability and efficacy of Empowered, Queer, Quitting, and Living--New Mexico (EQQUAL-NM), a smoking cessation intervention for sexual and gender minority young adults in New Mexico. Smoking prevalence among sexual and gender minority (SGM) adults in New Mexico is more than twice as high as non-SGM adults. Helping young adult tobacco users to quit is critical, yet there have been few efforts to develop tailored treatments specifically for this population. EQQUAL-NM is a digital smoking cessation intervention designed specifically for SGM young adult smokers in New Mexico and may help them quit smoking.

Read the detailed description

OUTLINE:

Participants are randomized to 1 of 2 groups.

GROUP I: Participants receive access to a self-guided, smartphone app-delivered quit smoking program, called EQQUAL-NM (Program A) that helps explore personal values and teaches participants about smoking triggers and skills to help them manage cravings and accept thoughts and feelings related to smoking. Participants receive text message reminders and prompts on study. Some participants also undergo collection of a saliva sample during follow-up.

GROUP II: Participants receive access to a self-guided, smartphone app-delivered quit smoking program, called EQQUAL-NM (Program B) that is based on current clinical practice guidelines for tobacco cessation to help them quit smoking. This program helps with quit advice, tracking progress on quitting smoking, and managing cravings. Participants receive text message reminders and prompts on study. Some participants also undergo collection of a saliva sample during follow-up.

After completion of study intervention, patients are followed up at 3 months.

02

Conditions studied

  • Cigarette Smoking-Related Carcinoma
03

In context

Lead sponsor

Fred Hutchinson Cancer Center is the lead sponsor of 537 studies on the registry; 79 are open to participants now.

Of its 57 completed or terminated interventional studies of FDA-regulated products, 45 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Self-identify being between 18 and 30 years of age
  • Self-identify as a sexual and/or gender minority (i.e., a sexual orientation other than straight and/or gender that doesn't match sex assigned at birth)
  • Currently reside in New Mexico, with a New Mexico mailing address, and anticipate remaining in New Mexico for the duration of the study (3 months)
  • Self-report smoking at least 1 cigarette per week in the 30 days prior to screening
  • Own an Android phone or iPhone
  • Have at least weekly internet access for the next three months
  • Willing and able to stream audio and video for this study
  • Current use of a personal email account
  • Current use of text messaging
  • Interested in participating in the study for themselves (versus [vs] someone else)
  • Self-report that they have not participated in one of Fred Hutch's/NMSU's prior smoking cessation studies
  • Understand and agree to the conditions of compensation
  • Currently not incarcerated
  • Participants must be willing to use the assigned intervention program, complete the study assessments, and agree to the online consent form in English

Exclusion criteria

Exclusion Criteria:

  • Current use of other tobacco cessation treatments at the time of screening, including pharmacotherapy or behavioral support (but initiating these treatments during the study is allowed)
  • Member of the same household as another research participant
  • Previous use of the National Cancer Institute (NCI) QuitGuide app
  • Google voice number as sole phone number
  • Does not pass study fraud prevention protocol
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Arm I (EQQUAL-NM, Program A)

    Participants receive self-guided smartphone app-delivered EQQUAL-NM (Program A) intervention on study. Participants also receive motivational messages, reminders and smoking cessation information via text messages. Some participants also complete at-home saliva sample collection during follow-up.

    Behavioral: Smartphone App-delivered Smoking Cessation Intervention · Other: Health Promotion and Education · Other: Biospecimen Collection · Other: Questionnaire Administration

  • Active comparator
    Arm II (EQQUAL-NM, Program B)

    Participants receive self-guided smartphone app-delivered EQQUAL-NM (Program B) intervention on study. Participants also receive motivational messages, reminders and smoking cessation information via text messages. Some participants also complete at-home saliva sample collection during follow-up.

    Behavioral: Smartphone App-delivered Smoking Cessation Intervention · Other: Health Promotion and Education · Other: Biospecimen Collection · Other: Questionnaire Administration

Interventions

  • BehavioralSmartphone App-delivered Smoking Cessation Intervention

    Receive access to EQQUAL-NM (Program A) intervention

    Also known as: Smoking and Tobacco Use Cessation Intervention

  • BehavioralSmartphone App-delivered Smoking Cessation Intervention

    Receive access to EQQUAL-NM (Program B) intervention

    Also known as: Smoking and Tobacco Use Cessation Intervention

  • OtherHealth Promotion and Education

    Receive text message reminders, motivational messages and prompts via SMS text messages (Program A)

    Also known as: Text Message-Based Intervention

  • OtherHealth Promotion and Education

    Receive text message reminders, motivational messages and prompts via SMS text messages (Program B)

    Also known as: Text Message-Based Intervention

  • OtherBiospecimen Collection

    Complete at-home saliva sample collection

    Also known as: Saliva Sample Collection

  • OtherQuestionnaire Administration

    Ancillary studies

06

What researchers measure

Primary outcomes

  1. Participant satisfaction

    Self-report of satisfaction overall and with specific program components will be rated on a 5-point Likert-type scale. Higher scale scores indicate higher satisfaction with the app.

    Time frame: At 3-month follow-up

  2. Number of logins to the assigned application

    Server-recorded number of app openings over 3 months

    Time frame: Up to 3-month follow-up

Secondary outcomes

  1. Self-reported 7-day point prevalence abstinence (PPA) from all nicotine and tobacco products

    Self-report of no nicotine/tobacco product use over the previous 7 days, with the exception of FDA-approved medications

    Time frame: At 3 months

  2. Biochemically confirmed 7-day point prevalence abstinence (PPA) from all nicotine/tobacco products

    Self-report of no nicotine/tobacco product use over the previous 7 days, with the exception of FDA-approved medications, biochemically confirmed via saliva cotinine

    Time frame: At 3 months

  3. Self-reported 30-day PPA from all nicotine/tobacco products

    Self-report of no nicotine/tobacco product use over the previous 30 days, with the exception of FDA-approved medications

    Time frame: At 3 months

  4. Biochemically confirmed 30-day PPA from all nicotine/tobacco products

    Self-report of no nicotine/tobacco product use over the previous 30 days, with the exception of FDA-approved medications, biochemically confirmed via saliva cotinine

    Time frame: At 3 months

  5. Self-reported 7-day PPA from cigarette smoking

    Self-report of no cigarette smoking over the previous 7 days

    Time frame: At 3 months

  6. Self-reported 30-day PPA from cigarette smoking

    Self-report of no cigarette smoking over the previous 30 days

    Time frame: At 3 months

  7. Change in Contemplation Ladder scores

    Contemplation Ladder scores will be used to assess readiness to quit using cigarettes. Ladder scores are on a 0 to 10 scale, with higher change scores meaning greater increases readiness to quit.

    Time frame: At baseline and at 3-month follow-up

  8. Change in acceptance of tobacco-use triggers

    Change in acceptance of tobacco-use triggers will be measured using the Avoidance and Inflexibility Scale. Higher change scores indicate greater improvement in acceptance of tobacco use triggers.

    Time frame: At baseline and at 3-month follow-up

  9. Change in values-guided action

    Change in values-guided action measured using the Values Questionnaire. Higher change scores indicate greater improvement in values-guided action.

    Time frame: At baseline and at 3-month follow-up

07

Study locations

1 site
  • Fred Hutch/University of Washington Cancer Consortium
    Seattle, Washington 98109, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06386432
Lead sponsor
Fred Hutchinson Cancer Center
Collaborators
National Cancer Institute (NCI), National Cancer Institute Center to Reduce Cancer Health Disparities, New Mexico State University
Responsible party
Sponsor
First posted
Apr 26, 2024
Start date
Dec 1, 2025 (estimated)
Primary completion
Apr 1, 2026 (estimated)
Completion
Apr 1, 2026 (estimated)
Last update
Oct 8, 2025

Study contacts

Jaimee Heffner
principal investigator · Fred Hutch/University of Washington Cancer Consortium

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion