- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT03002883
STAND Community College Tobacco Cessation Trial
Sacramento Taking Action Against Nicotine Dependence (STAND) at Sacramento City College
Community colleges have 45% of the nation's undergraduates and have a higher smoking prevalence rate than 4-year colleges. California's community colleges comprise the nation's largest higher education system, and Sacramento has the second largest community college district. As more colleges are encouraged to become smoke and tobacco-free campuses, smokers enrolled at community college campuses need greater support. However, community colleges may lack the student health clinic resources that 4-year colleges have for students who live on campus. Little evidence to date demonstrates effective interventions for smokers on community college campuses.
This pilot study seeks to demonstrate the feasibility and promising outcomes of two cessation interventions, compared with usual care on a community college campus. The first intervention was based on a promising model of brief motivational interviewing delivered by peer educators, developed by the community lead Breathe California of Sacramento-Emigrant Trails (BCSET) through the Sacramento Taking Action Against Tobacco Dependence (STAND) project. The second intervention was based on direct enrollment into the California Smokers' Helpline, which has demonstrated utility for promoting smoking cessation among young adults with low socioeconomic status. Usual care consisted of students going to the student health center for smoking cessation assistance.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- adult 18 years or older
- current smoker in the past 30 days
- smoker wants to quit
- smoker not currently participating in other smoking cessation activities, and
- smoker must be willing to accept randomization into any of the 3 study arms
Exclusion Criteria:
- students not proficient in communicating in English
- adults unable to consent
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Placebo-Komparator: Usual Care
Students referred to student health for tobacco cessation resources including campus "Quit Kits"
|
Participant provided "Quit Kit" water bottle with small cessation aids (eg.
sunflower seeds) and educated about student health as a cessation resource
|
|
Aktiver Komparator: Brief Motivational Interviewing
Students received brief motivational interviewing by a student peer educator about tobacco cessation
|
Participant provided "Quit Kit" water bottle with small cessation aids (eg.
sunflower seeds) and educated about student health as a cessation resource
Peer educator conducts brief motivational interviewing about smoking cessation and participant goals
|
|
Aktiver Komparator: Direct referral to quitline
Students were directly referred to the state quitline for follow-up counseling
|
Participant provided "Quit Kit" water bottle with small cessation aids (eg.
sunflower seeds) and educated about student health as a cessation resource
Peer educator educates about state quitline services and gets verbal consent to use quitline's direct referral web portal for quitline to contact participant in 1-2 business days about free counseling services to make a quit plan
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Biochemically validated smoking cessation
Zeitfenster: 6 months
|
Point prevalence abstinence validated by saliva cotinine level
|
6 months
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Self-reported smoking cessation
Zeitfenster: 6 months
|
Point prevalence abstinence by self-report on survey
|
6 months
|
|
Self-reported smoking cessation
Zeitfenster: 3 months
|
Point prevalence abstinence by self-report on survey
|
3 months
|
|
Self-reported smoking cessation
Zeitfenster: 1 month
|
Point prevalence abstinence by self-report on survey
|
1 month
|
Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Elisa Tong, MD, University of California, Davis
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- 491744
- 22BT-0057 (Andere Kennung: Other)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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