Implementing Screening and Brief Interventions for Excessive Drinkers in Primary Health Care

NCT02968186 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 222

Last updated 2020-01-13

No results posted yet for this study

Summary

The objective of this study is to investigate the efficacy of an implementation program specifically designed to increase alcohol screening and brief intervention rates in primary health care.

Conditions

  • Alcohol-Related Disorders

Interventions

BEHAVIORAL

Implementation program

Health professionals in the intervention arm will receive up to four training sessions in the first three months of the implementation period. Practice support will be continuously available throughout the project. Posters specifically designed for this project will be added to the primary health care units aiming to facilitate eliciting alcohol issues during the consultations, and to help professionals remembering to conduct alcohol screening and brief intervention. Leaflets to be handed-in to patients were also specifically produced for this project, aiming to aid professionals in advising at-risk drinkers to cut down. The research team will schedule with each primary health care unit regular visits for feedback on the progress of the program.

Sponsors & Collaborators

  • University of Cambridge

    collaborator OTHER
  • University of Stirling

    collaborator OTHER
  • Université Catholique de Louvain

    collaborator OTHER
  • Agrupamento de Centros de Saúde de Dão Lafões

    lead OTHER

Principal Investigators

  • Frederico M Rosário, MD · Dão Lafões Grouping of Primary Health Care Centres

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2018-03-31
Completion
2018-07-31

Countries

  • Portugal

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02968186 on ClinicalTrials.gov