- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01168726
Protective Behavioral Strategies and Brief Alcohol Interventions
15 juni 2017 uppdaterad av: Matthew P. Martens, University of Missouri-Columbia
Excessive college student drinking represents an important public health problem for both the students themselves and those with whom they interact.
The objective of this research is to better understand how to reduce such high-risk drinking by improving prevention and treatment programs, which will provide an overall public health benefit.
Subjects in the study will be randomized to one of two brief intervention conditions or an education-only control condition.
It is hypothesized that those in the intervention conditions will report greater reductions in alcohol use and alcohol-related problems than those in the control condition.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
The primary objective of this project is to examine factors that are associated with the effectiveness of intervention programs designed to reduce high-risk drinking among heavy drinking college students.
Previous research has found similar effect sizes for different types of multi-component, brief interventions among college students, but little research has assessed the degree to which specific components of such interventions are associated with intervention outcomes.
One common component of motivational enhancing interventions among college students involves providing cognitive-behavioral self-control strategies designed to reduce one's use of alcohol, which we term "protective behavioral strategies" (PBS).
However, there are two important factors that limit our understanding of the effects of PBS on client outcomes.
First, the use of these strategies in motivational enhancing programs has generally not been assessed in a systematic manner, due in part to the fact that until recently a standardized measure of such strategies did not exist.
Second, researchers have yet to conduct studies that dismantle the specific effects associated with the PBS component on client outcomes.
That is, studies have not tested interventions with and without assessment and feedback regarding a client's use of PBS.
Participants in this project will be "at-risk" college student drinkers who will be assigned to one of three conditions: a brief intervention that includes a focus on PBS, a brief intervention that does not include this focus, and an education-only control condition.
Participant will complete self-report measures of alcohol-related variables at baseline, 30-day, and 6-month follow-ups.
Mixed-model analyses will be used to determine the effectiveness of the intervention programs, and structural equation modeling will be used to determine if increases in PBS result in reductions in alcohol use/alcohol-related problems.
Studietyp
Interventionell
Inskrivning (Faktisk)
365
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Missouri
-
Columbia, Missouri, Förenta staterna, 65211
- University of Missouri
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 24 år (Vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- At least one binge drinking episode in the preceding month
Exclusion Criteria:
- At-risk for alcohol dependence or major depressive disorder
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Protective Behavioral Strategies
Personalized feedback on use of protective behavioral strategies.
|
Personalized feedback on use of protective behavioral strategies.
|
|
Experimentell: Personalized Normative Feedback
Personalized feedback on how one's own drinking compares to relevant norms.
|
Personalized feedback on how one's own drinking compares to relevant norms.
|
|
Aktiv komparator: Alcohol Education
Educational information about harms associated with heavy drinking.
|
Educational information about harms associated with heavy drinking.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Drinks Per Week
Tidsram: 6 Months
|
6 Months
|
|
|
Rutgers Alcohol Problems Index (RAPI)
Tidsram: 6 months
|
Total scores on an alcohol problems scale.
Possible score range = 0-92.
Higher scores are indicative of more alcohol-related problems.
|
6 months
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Drinking Norms Rating Form
Tidsram: 6 months
|
Perceived drinking among other students, represented by standardized scores on the Drinking Norms Rating Form.
Higher values indicate that the individual perceives higher levels of drinking among other students.
Because the scores are standardized their is no hypothetical minimum or maximum, and the scale is standardized with a mean of 0 and standard deviation of 1. So, a mean value of 1.52 means that participants in that condition had an average score that was 1.52 standard deviation above the overall mean of the sample.
|
6 months
|
|
Protective Behavioral Strategies Scale.
Tidsram: 6 months
|
Use of protective behavioral strategies related to alcohol use.
Higher scores indicate more use of the strategies.
A total score was calculated by summing the three subscale scores on the measure (range = 3-18).
|
6 months
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Matthew P Martens, PhD, University of Missouri-Columbia
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 januari 2010
Primärt slutförande (Faktisk)
1 september 2010
Avslutad studie (Faktisk)
1 september 2010
Studieregistreringsdatum
Först inskickad
20 juli 2010
Först inskickad som uppfyllde QC-kriterierna
21 juli 2010
Första postat (Uppskatta)
23 juli 2010
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
13 juli 2017
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
15 juni 2017
Senast verifierad
1 juni 2017
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- Protective Behaviors
- 1R21AA016779-01A2 (U.S.S. NIH-anslag/kontrakt)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .