Smoking Cessation Via Text Messaging: Feasibility Testing of Stop My Smoking USA (SMS USA)
28. april 2016 oppdatert av: Center for Innovative Public Health Research
Smoking Cessation Via Text Messaging: Feasibility Testing of SMS USA
The investigators developed a text messaging-based smoking cessation program called SMS (Stop My Smoking) USA.
It was tailored for the unique needs and smoking habits of young adults.
The investigators hypothesized that those in the SMS USA intervention would be significantly more likely to be quit at 6-months compared to the attention-matched control group.
Studieoversikt
Detaljert beskrivelse
About one in four young adults are current smokers.
Although over half report the desire to quit or cut down, quit rates in this age group have remained stagnant in the last ten years.
Text messaging may represent a compelling intervention delivery method for smoking cessation for young adults because it is a medium they have widely adopted.
Cell phone interventions also are unique because of their 'always on' capability - interventions are never far from the young adult's reach and they are received automatically instead of requiring the participant to initiate contact in order to receive the information.
Dr. Ybarra, along with Drs.
Holtrop and Graham, have developed SMS Turkey, an innovative behavioral intervention that uses text messaging to deliver CBT-based smoking cessation information to participants daily.
Successful use of text messaging to deliver smoking cessation programs has been reported by Rodgers and colleagues in New Zealand and a replication study they are leading in the United Kingdom.
These data provide optimism for the feasibility of text messaging-based smoking cessation programs in the United States.
Using qualitative methods to inform design and content, and quantitative methods to assess the feasibility of the program, we propose to design and test SMS (Stop My Smoking) USA, a cell-phone based smoking cessation program for young adults ages 18-25.
This innovative smoking cessation program uses technology widely adopted by young adults, an under-targeted population, to deliver a proactive, cognitive behavioral therapy (CBT)-based intervention.
Our multidisciplinary team of researchers brings together expertise in Internet health and the design of tailored smoking cessation interventions.
Studietype
Intervensjonell
Registrering (Faktiske)
164
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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California
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Santa Ana, California, Forente stater, 92705
- Internet Solutions for Kids, Inc.
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 25 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- 28 cigarettes or more per week (at least 4/day) and on at least 6 days/week.
- Owning a text-capable cell phone and cognizant of how to send and receive text messages
- Currently enrolled or intending to enroll in an unlimited text messaging plan
- Enrolled with a cell phone carrier that was compatible with the program software
- Agree to verification of smoking cessation status by a significant other
- Able to read and write in English
- Informed consent
Exclusion Criteria:
None
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: SMS USA
The 6-week smoking cessation intervention
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Intervention participants receive text messages daily pre-and post-quit.
Everyone receives messages 14 days prior to the Quit day, and through the day after Quit.
Then, participants are 'pathed' to particular messages based upon their self-reported smoking status at Day 2 and Day 7 post quit, respectively.
Those who are successful at quitting receive messages aimed at relapse prevention whereas those who have slipped receive messages aimed at getting the person to recommit to quitting and trying again.
Andre navn:
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Ingen inngripen: Attention matched control
Messages aimed at improving one's sleep and increasing one's fitness, along with general messages about the most well known health dangers of smoking.
Messages sent on the same schedule as the intervention group.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Continuous Abstinence at 3-months Assessed in Accordance With the NIH Behavior Change Consortium's Recommendations
Tidsramme: 3-months post-quit
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Continuous abstinence is defined as 5 or fewer cigarettes smoked since one's quit date. The question was asked based upon West et al., 2005: "Have you smoked at all, even just a puff, since [insert quit date]?" If yes, the respondent will be probed for how many cigarettes were smoked. Responses will be categorized into one of three options: A) No, not a puff; B) 1-5 cigarettes; C) More than 5 cigarettes. Self-reported cessation is confirmed by a significant other. |
3-months post-quit
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Point Prevalence
Tidsramme: 4-weeks post-quit
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A cigarette, even just a puff, within the last 7 days (yes/no).
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4-weeks post-quit
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Continuous Abstinence at 4-weeks Post-quit
Tidsramme: 4 weeks post-quit
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Smoking five or fewer cigarettes since quit day at 4 weeks post-quit as verified by a significant other
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4 weeks post-quit
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Generelle publikasjoner
- Ybarra ML, Holtrop JS, Prescott TL, Strong D. Process evaluation of a mHealth program: lessons learned from Stop My Smoking USA, a text messaging-based smoking cessation program for young adults. Patient Educ Couns. 2014 Nov;97(2):239-43. doi: 10.1016/j.pec.2014.07.009. Epub 2014 Jul 17.
- Ybarra ML, Prescott TL, Holtrop JS. Steps in tailoring a text messaging-based smoking cessation program for young adults. J Health Commun. 2014 Dec;19(12):1393-407. doi: 10.1080/10810730.2014.901441. Epub 2014 Apr 25.
- Filion AJ, Darlington G, Chaput JP, Ybarra M, Haines J. Examining the influence of a text message-based sleep and physical activity intervention among young adult smokers in the United States. BMC Public Health. 2015 Jul 16;15:671. doi: 10.1186/s12889-015-2045-2.
- Ybarra ML, Holtrop JS, Prescott TL, Rahbar MH, Strong D. Pilot RCT results of stop my smoking USA: a text messaging-based smoking cessation program for young adults. Nicotine Tob Res. 2013 Aug;15(8):1388-99. doi: 10.1093/ntr/nts339. Epub 2013 Jan 24.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. juni 2009
Primær fullføring (Faktiske)
1. desember 2011
Studiet fullført (Faktiske)
1. desember 2011
Datoer for studieregistrering
Først innsendt
15. mars 2011
Først innsendt som oppfylte QC-kriteriene
24. januar 2012
Først lagt ut (Anslag)
25. januar 2012
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
6. juni 2016
Siste oppdatering sendt inn som oppfylte QC-kriteriene
28. april 2016
Sist bekreftet
1. april 2016
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- R21CA135669 (U.S. NIH-stipend/kontrakt)
- 5R21CA135669 (U.S. NIH-stipend/kontrakt)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Studiedata/dokumenter
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Skjema for informert samtykke
Informasjonskommentarer: All study materials (e.g., consent form, assessments) can be downloaded from the project website
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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Lions Club International FoundationFullført
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Chinese University of Hong KongFullførtUtnyttelse av poliklinisk koloskopitjenesteHong Kong
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Lovisenberg Diakonale HospitalUkjentOtorhinolaryngologiske sykdommer | Hørselsforstyrrelser | Søvnforstyrrelser