- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01096108
Quit and Win Contests to Improve Smoking Cessation Among College Students
Enhancing Quit and Win Contests to Improve Smoking Cessation Among College Students
Standard Quit and Win contests, in which smokers typically quit for one month in return for the opportunity to win prizes, are simple and easy to implement and may be cost-effective in encouraging smokers to quit. By extending contest length and enhancing counseling content, Quit and Win contests may be more effective at encouraging smoking abstinence.
This study aims to evaluate the efficacy of extended and content-enhanced Quit and Win contests to enhance smoking abstinence at college campuses.
Studieoversikt
Status
Forhold
Detaljert beskrivelse
Participants will be randomized to 1 of 4 treatment groups with varying counseling treatments and contest lengths. All participants receive a 2 week supply of nicotine replacement therapy (NRT) and weekly support emails. Follow-up assessment surveys occur at 1, 3, 4 and 6 months post enrollment.
Participants who have completed the follow-up assessment surveys and self-reported that they are tobacco-free will be asked to provide a urine sample in order to verify abstinence.
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
Minnesota
-
Minneapolis, Minnesota, Forente stater, 55455
- Masonic Cancer Center, University of Minnesota
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Enrolled full or part-time at one of the participating campuses
- Smoke at least 10 days per month
- Intending to be in school for the entire academic year (i.e., next 2 semesters)
- Willing to provide a baseline urine sample to verify smoking status
- Able to read English
- Access to working telephone for phone-based counseling and surveys
- Access to a computer with internet access
- Provide written informed consent
Exclusion Criteria:
- Prior to concurrent enrollment in this study through a different college campus or in a different academic year
- those who have used a cessation aid within the last 7 days
- pregnant or planning to become pregnant in next 3 months
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Tildeling: Randomisert
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: Standard Contest
Smoking abstinence, 1 prize award (month 1)
|
Smoking abstinence, 1 prize award (month 1)
|
Eksperimentell: Standard Contest plus MAPS
Smoking abstinence, 1 prize award (month 1) plus motivational and problem-solving counseling (MAPS - Counseling phone calls); 20 weeks.
|
Smoking abstinence, 1 prize award (month 1)
Counseling phone calls
|
Eksperimentell: Extended Contests
Smoking abstinence, 3 contest prize awards (contests 1, 2 and 3)
|
Smoking abstinence, 3 contest prize awards (contests 1, 2 and 3)
|
Eksperimentell: Extended Contests plus MAPS
Extended quit and win contests (3 successive monthly contests) plus motivational and problem-solving counseling (MAPS).
{Smoking abstinence, 3 contest prize awards (contests 1, 2 and 3) plus Counseling phone calls.
|
Counseling phone calls
Smoking abstinence, 3 contest prize awards (contests 1, 2 and 3)
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Efficacy of extended versus standard quit and win contests
Tidsramme: 6 Months
|
The aim is to evaluate the separate and combined efficacy of increased dose of treatment and adding counseling to enhance smoking abstinence among college students
|
6 Months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Efficacy of motivational and problem solving counseling versus no counseling
Tidsramme: 6 Months
|
The aim is to 1) determine relative cost-effectiveness of extended incentives and motivational and problem-solving (MAPS) counseling.
2) Examine potential mediators and moderators of intervention effects.
|
6 Months
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Janet L Thomas, Ph.D., Masonic Cancer Center, University of Minnesota
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- 2008NTLS155
- 0901S57761 (Annen identifikator: IRB, University of Minnesota)
- R01 HL093114-01 (Annet stipend/finansieringsnummer: National Heart, Lung, and Blood Institute)
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