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Completed

NCT Number: NCT02968186

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dão Lafões Grouping of Primary Health Care Centres

Viseu, Dão Lafões, 3514-511, Portugal

About this study

Alcohol is an important risk factor for several diseases, even when consumed moderately. Screening and advising at-risk drinkers to cut-down is a highly effective and cost-effective intervention when conducted in primary healthcare settings. However, these interventions are seldom implemented at the primary care level.

Twelve out of the 26 primary health care units of the Dão Lafões Grouping of Primary Health Care Centres will be randomized to two groups: the intervention arm will receive the new implementation program; the control group will be on a waiting list for receiving the implementation program and will receive the intervention after the testing phase of the trial is completed. The study will last for one year, starting in January 2017. The implementation program was designed in order to overcome known barriers for implementing alcohol screening and brief advice in primary health care. The Behaviour Change Wheel and the Theoretical Domains Framework were used to pinpoint the constructs and behaviour change techniques most suited to address the barriers in order to achieve practice changes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Primary health care units of the Dão Lafões Grouping of Primary Health Care Centres (family physicians/general practitioners, family medicine residents, practice nurses and receptionists)

Exclusion criteria

  • Primary health care units with four or less general practitioners
  • Primary health care units that have a specific alcohol program already implemented

Treatment and study plan

Implementation program

Behavioral

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.

Primary outcomes

  1. Alcohol screening rate

    Time frame: 12 months

    Percentage of eligible patients visiting the primary health care centre for an appointment with a general practitioner or nurse who were screened for alcohol use with the Alcohol Use Disorders Identification Test

Secondary outcomes

  1. Improvement of general practitioners attitudes toward at-risk drinkers

    Time frame: 12 months

    Short Alcohol and Alcohol Problems Perception Questionnaire given before and after intervention. General practitioners are classified into a more positive or more negative attitudes group based on the answers given. The groups will be compared before and after.

  2. Improvement in knowledge related to alcohol screening and brief intervention

    Time frame: 12 months

    Four multiple choice questions. These questions will measure the theoretical knowledge of health professionals to key concepts related to alcohol screening and brief intervention. The groups will be compared before and after.

  3. Improvement in barriers for implementing alcohol screening and brief intervention

    Time frame: 12 months

    Level of agreement with 33 statements. Each statement can be mapped to a specific domain of the Theoretical Domains Framework. The groups will be compared before and after.

  4. Utility of materials used in the trial

    Time frame: Through study completion, an average of 12 months

    Level of agreement with 6 statements. Participants (intervention arm only) will be asked to rate the impact of the materials that were specifically produced to be used during the trial.

  5. Brief intervention rate

    Time frame: 12 months

    Percentage of patients who screened positive that were offered at least one brief intervention

Sponsors and collaborators

Lead sponsor

Agrupamento de Centros de Saúde de Dão Lafões

Other

Collaborators

  • University of Cambridge
  • University of Stirling
  • Université Catholique de Louvain

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Nov 18, 2016
Registry last updated
Jan 13, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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