Text Messaging-Based Smoking Cessation Program for Homeless Youth

NCT ID: NCT03874585

Last Updated: 2020-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1/PHASE2

Total Enrollment

77 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-30

Study Completion Date

2020-05-21

Brief Summary

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Unaccompanied homeless youth smoke at much higher rates than non-homeless adolescents and young adults. Many homeless youth smokers are motivated to quit; yet, strategies specifically developed for this vulnerable population are lacking. This study will develop and pilot test a text messaging intervention (also known as a TMI) to help homeless youth quit smoking. Text messaging can provide ongoing support for homeless youth during a quit attempt, which is important given that these youth tend to be highly mobile and lack regular access to health services. Participants in this study will be homeless youth who currently smoke and are motivated to quit smoking. All participants will receive a 30-minute group-based smoking cessation counseling session and a nicotine replacement product. Half of these smokers will also receive the TMI, for 6 weeks following the group counseling session, which will provide ongoing support for quitting. The main goal of this study is to investigate whether receiving the TMI results in greater reductions in cigarette smoking over a 3-month period compared to receiving the group counseling session alone.

Detailed Description

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Conditions

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Cigarette Smoking

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Standard Condition

Participants in the standard condition will receive a 30-minute group-based smoking cessation counseling session based on the 5 A's approach (Ask; Advise; Assess; Assist; Arrange) and free nicotine replacement.

Group Type ACTIVE_COMPARATOR

Group counseling and nicotine replacement

Intervention Type BEHAVIORAL

Participants will receive a 30-minute group smoking cessation counseling session and a supply of nicotine replacement.

Enhanced Condition

Participants in the standard condition will receive a 30-minute group-based smoking cessation counseling session based on the 5 A's approach (Ask; Advise; Assess; Assist; Arrange), free nicotine replacement, and the 6-week text messaging intervention.

Group Type EXPERIMENTAL

Group counseling, nicotine replacement, and text messaging support

Intervention Type BEHAVIORAL

Participants will receive a 30-minute group smoking cessation counseling session, a supply of nicotine replacement, and the 6-week text messaging intervention to provide ongoing support for quitting

Interventions

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Group counseling and nicotine replacement

Participants will receive a 30-minute group smoking cessation counseling session and a supply of nicotine replacement.

Intervention Type BEHAVIORAL

Group counseling, nicotine replacement, and text messaging support

Participants will receive a 30-minute group smoking cessation counseling session, a supply of nicotine replacement, and the 6-week text messaging intervention to provide ongoing support for quitting

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* between ages of 18-25
* seeking services at one of the participating drop-in centers for homeless youth
* smoked at least 5 cigarettes per day on at least 20 days in the past month
* motivated to quit in next 30 days
* has a cell phone to receive text messages and willing to receive text messages

Exclusion Criteria

* currently pregnant or breastfeeding, or planning to become pregnant or breastfeed in the next 6 months
* has a medical condition (based on self-report) which would prevent using the nicotine replacement product
* used pharmacotherapy to reduce or stop smoking in the past 30 days
* currently receiving other smoking cessation services
Minimum Eligible Age

18 Years

Maximum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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RAND

OTHER

Sponsor Role lead

Responsible Party

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Joan Tucker

Senior Behavioral Scientist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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My Friend's Place

Los Angeles, California, United States

Site Status

Los Angeles LGBT Center Youth Center

Los Angeles, California, United States

Site Status

Safe Place for Youth

Venice, California, United States

Site Status

Countries

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United States

References

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Pedersen ER, Linnemayr S, Shadel WG, Zutshi R, DeYoreo M, Cabreros I, Tucker JS. Substance Use and Mental Health Outcomes from a Text Messaging-Based Intervention for Smoking Cessation Among Young People Experiencing Homelessness. Nicotine Tob Res. 2022 Jan 1;24(1):130-134. doi: 10.1093/ntr/ntab160.

Reference Type DERIVED
PMID: 34375409 (View on PubMed)

Tucker JS, Linnemayr S, Pedersen ER, Shadel WG, Zutshi R, DeYoreo M, Cabreros I. Pilot Randomized Clinical Trial of a Text Messaging-Based Intervention for Smoking Cessation Among Young People Experiencing Homelessness. Nicotine Tob Res. 2021 Aug 29;23(10):1691-1698. doi: 10.1093/ntr/ntab055.

Reference Type DERIVED
PMID: 33852730 (View on PubMed)

Linnemayr S, Zutshi R, Shadel W, Pedersen E, DeYoreo M, Tucker J. Text Messaging Intervention for Young Smokers Experiencing Homelessness: Lessons Learned From a Randomized Controlled Trial. JMIR Mhealth Uhealth. 2021 Apr 1;9(4):e23989. doi: 10.2196/23989.

Reference Type DERIVED
PMID: 33792551 (View on PubMed)

Tucker JS, Pedersen ER, Linnemayr S, Shadel WG, DeYoreo M, Zutshi R. A text message intervention for quitting cigarette smoking among young adults experiencing homelessness: study protocol for a pilot randomized controlled trial. Addict Sci Clin Pract. 2020 Feb 19;15(1):11. doi: 10.1186/s13722-020-00187-6.

Reference Type DERIVED
PMID: 32075695 (View on PubMed)

Other Identifiers

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27IP-0051

Identifier Type: -

Identifier Source: org_study_id

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