Peer-led Brief Alcohol Intervention for College Student Drinkers in Spain

Sponsor
Clinica Universidad de Navarra, Universidad de Navarra (Other)
Overall Status
Completed
CT.gov ID
NCT05437484
Collaborator
(none)
50
1
2
20.9
2.4

Study Details

Study Description

Brief Summary

A pilot randomized controlled trial was carried out. Fifty nursing students were randomly assigned either a 50-minute brief motivational intervention with individual feedback or a treatment-as-usual control condition. The intervention was delivered by undergraduate peer counsellors trained in Brief Alcohol Screening and Intervention for College Students. Primary outcomes for testing efficacy were alcohol use and alcohol-related consequences.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Peer-led BASICS
N/A

Detailed Description

Aims: To assess the potential efficacy and the feasibility of a peer-led brief alcohol intervention aimed to reduce the alcohol consumption in Spanish heavy nursing student drinkers.

Methods: A pilot randomized controlled trial was carried out. Fifty nursing students were randomly assigned either a 50-minute brief motivational enhancement intervention with individual feedback (n=23) or a treatment-as-usual control condition (n=27). Both motivational interviewing and personalized feedback were delivered by undergraduate peer counsellors trained in Brief Alcohol Screening and Intervention for College Students (BASICS). Participants were assessed during their pledge year of university with a one-month follow-up. Primary outcomes for testing efficacy were alcohol use (quantity, heavy-drinking episodes, and peak blood alcohol concentration), and alcohol-related consequences. Quantitative data were analyzed using the U-Mann-Whitney and Wilcoxon test. Content analysis was used for measuring the feasibility of the program.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
Design, Implementation and Evaluation of a Peer-led Alcohol Prevention Intervention for College Students. A Exploratory Trial
Actual Study Start Date :
Sep 2, 2019
Actual Primary Completion Date :
Apr 30, 2020
Actual Study Completion Date :
May 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group: peer-led BASICS session

Participants randomized to the intervention group received a peer-led BASICS session.

Behavioral: Peer-led BASICS
The peer-led BASICS session consisted in a face-to-face 50-minute motivational interview. In this meeting, the peer counsellor oriented the participant using a personalized graphic feedback sheet, with topics including participant's drinking pattern; level of intoxication; perceived and actual descriptive drinking norms, alcohol expectancies; drinking consequences; individual risk factors; financial costs; alcohol caloric consumption, and hours of exercise required to burn those calories, and protective behavioral strategies. Participants received a copy of the personalized feedback, a personalized BAC card, and a tips sheet. BASICS facilitators were volunteer undergraduate nursing students from who attented a pre-training course and showed being competent to conduct BASICS-based motivational interview and knowledgeable about alcohol.

No Intervention: Control group

Participants randomized to the control group did not receive any specific intervention.

Outcome Measures

Primary Outcome Measures

  1. Change in 'Quantitaty of alcohol use in a typical weekend' (preliminary efficacy outcomes) [For measuring the change, there are two time points: pre-test and post-test (one month after receiving the programme)]

    Assesing the change in the total number of drinks during a typical weekend (Thursday, Friday, Saturday and Sunday) during the previous 30 days.

  2. Change in 'Estimated peak blood alcohol content (peak BAC)' (preliminary efficacy outcomes) [For measuring the change, there are two time points: pre-test and post-test (one month after receiving the programme)]

    Assesing the change in the estimated peak blood alcohol content. It was calculated using participants' responses about maximum drinks consumed on the occasion of highest consumption in the last month, and the number of hours they spent drinking on that occasion.

  3. Change in 'Frequency of binge drinking episodes' (preliminary efficacy outcomes) [For measuring the change, there are two time points: pre-test and post-test (one month after receiving the programme)]

    Assesing the change in the frequency of binge drinking episodes in the past month (5 or more (male)/ 4 or more (female) glasses of alcoholic beverages on the same drinking occasion).

  4. Change in 'Number of alcohol-related consequences (preliminary efficacy outcomes)' [For measuring the change, there are two time points: pre-test and post-test (one month after receiving the programme)]

    Assesing the change in the number of negative consequences associated with their alcohol consumption in the previous 30 days.

Secondary Outcome Measures

  1. Peer counselors' fidelity -adherence to motivational interviewing skills and alcohol-related content (feasibility outcomes) [From the beginning of the intervention sessions until the end of the intervention, an average of 3 months.]

    Peer counselors' fidelity to the implementation of the intervention, including adherence to the theoretical alchol-related content, and the use of MI skills during the intervention. For their measurement, an alcohol-related content checklist and the Peer Proficiency Assessment were used.

  2. Barriers and facilitators of the implementation process (feasibility outcomes) [From the beginning of the peer counsellors' training until the end of the intervention, an average of 9 months.]

    Factors that have affected positively and negatively during the program implementation.

  3. Acceptability -satisfaction- (feasibility outcomes) [From the beginning of the intervention sessions until the end of the intervention, an average of 3 months.]

    Satisfaction of both participants and peer counsellors with the program. It was used and ad-hoc questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 20 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • First year university students of Nursing Degree, between 18 and 20 years old.

  • Students of first access to the University.

  • Having had at least one episode of heavy drinking or binge drinking in the past month.

Exclusion Criteria:
  • Students who have started or previously studied other university degrees or a higher degree.

  • University students who do not consume alcohol or, if they do consume alcohol, have not had binge drinking in the last month.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Navarra Pamplona Navarra Spain 31008

Sponsors and Collaborators

  • Clinica Universidad de Navarra, Universidad de Navarra

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sara Pueyo, Clinical nurse, Clinica Universidad de Navarra, Universidad de Navarra
ClinicalTrials.gov Identifier:
NCT05437484
Other Study ID Numbers:
  • SP EXPLORATORIO
First Posted:
Jun 29, 2022
Last Update Posted:
Jun 29, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sara Pueyo, Clinical nurse, Clinica Universidad de Navarra, Universidad de Navarra
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2022