Evaluation of an Internet-based Intervention for Hazardous Drinkers
NCT ID: NCT01075685
Last Updated: 2010-11-10
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE2
1157 participants
INTERVENTIONAL
2009-10-31
2010-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Web-based alcohol programme
Participants could log on to their account and access the programme whenever they wanted to.
They received automated email reminders inviting them to use follow-up tools, especially the diary in order to register their alcohol intake on the previous week:
* 4 weeks after starting the programme, so that they would take advantage of the monitoring stage in case they had not spontaneously done so.
* 2 weeks later for 6-week follow-up.
interactive online programme to reduce alcohol consumption
The programme includes several steps:
* personalized feedback on alcohol consumption and related risks
* reviewing motivations and fears regarding drinking reduction
* analyse of drinking habits
* reduction goal setting
* follow-up tools (alcohol diary, craving scales, well-being scales)
* a final screen allowing participants to monitor their progress through graphs and automatically adapted comments.
Minimum information
Participants could log on to their account and access the programme whenever they wanted to. At 6 week follow-up they received an automated email reminder inviting them to use the diary in order to register their alcohol intake on the previous week.
Minimum information
This intervention includes:
* information about hazardous drinking
* an alcohol diary
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
interactive online programme to reduce alcohol consumption
The programme includes several steps:
* personalized feedback on alcohol consumption and related risks
* reviewing motivations and fears regarding drinking reduction
* analyse of drinking habits
* reduction goal setting
* follow-up tools (alcohol diary, craving scales, well-being scales)
* a final screen allowing participants to monitor their progress through graphs and automatically adapted comments.
Minimum information
This intervention includes:
* information about hazardous drinking
* an alcohol diary
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Institut national de prevention et d'education pour la sante
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Institut national de prevention et d'education pour la sante
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Juliette Guillemont, MS
Role: PRINCIPAL_INVESTIGATOR
Institut national de prevention et d'education pour la sante
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Evalcoometre
Identifier Type: -
Identifier Source: org_study_id