Preventing Risky Drinking in Veterans Treated With Prescription Opioids
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Faktiske)
Tilmelding
Fase
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Pennsylvania
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Philadelphia, Pennsylvania, Forenede Stater, 19104
- University of Pennsylvania
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Philadelphia, Pennsylvania, Forenede Stater, 19104
- Philadelphia VA Medical Center
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Pittsburgh, Pennsylvania, Forenede Stater, 15261
- VA Pittsburgh Health System
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- currently be receiving daily treatment with a prescription opioid for chronic pain;
- be 18 years or older;
- have a cell phone capable of receiving text messages;
- and be willing to be in a study where they might receive text messages.
Exclusion Criteria:
- meet DSM-V criteria for a moderate to severe alcohol or drug disorder (with the exception of nicotine abuse/dependence);
- have a current psychotic disorder severe enough to require inpatient treatment;
- are participating in substance abuse treatment at the VA or elsewhere (with exception of screening and brief intervention at the VA).
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Aktiv komparator: Standard Care
In this arm, veterans receive the care that they would receive had they not enrolled in the research.
No one will receive less than standard care.
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Eksperimentel: Prevention Intervention
An adaptive monitoring intervention, delivered through text messages and brief telephone calls, that can provide extended prevention services for veterans engaging in risky alcohol use.
After a veteran receives a BI for risky drinking, we will monitor alcohol use for 4 weeks.
Veterans who reduce alcohol use to safe levels will be placed in a monitoring track, which consists of tailored text messages and brief monthly telephone contacts.
Conversely, veterans who continue to use alcohol at hazardous levels will be placed in a track that provides tailored text messages and more frequent telephone calls.
These calls provide further prevention/intervention services to help the veteran reduce alcohol use.
These services address motivational issues and identify more effective ways to cope with stress and other factors that trigger unsafe alcohol use.
Information on the veteran's progress is used to guide the content of subsequent text messages and prevention interventions.
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Rates of Risky Drinking, Week 13
Tidsramme: weeks 1 - 13
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The primary outcome measure will be rates of the presence of any risky drinking in each week (i.e., more than 4 drinks per drinking day) as reported on the Time Line Follow Back.
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weeks 1 - 13
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Rates of Risky Drinking, Week 26
Tidsramme: weeks 14 - 26
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Rates of the presence of any risky drinking in each week (14 - 26)
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weeks 14 - 26
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Rates of Risky Drinking, Week 39
Tidsramme: weeks 27 - 39
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Rates of the presence of any risky drinking in each week (27 - 39)
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weeks 27 - 39
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Rates of Risky Drinking, Week 52
Tidsramme: weeks 40 - 52
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Rates of the presence of any risky drinking in each week (40 - 52)
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weeks 40 - 52
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Rates of Risky Drinking, Week 78
Tidsramme: weeks 53 - 78
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Rates of the presence of any risky drinking in each week (53 - 78)
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weeks 53 - 78
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Efterforskere
Efterforskere
- Ledende efterforsker: James R McKay, PhD, University of Pennsylvania
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Faktiske)
Primær færdiggørelse
Studieafslutning (Faktiske)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 818671
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