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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02642757
Other study ID # 14-214
Secondary ID SM14I0033
Status Completed
Phase N/A
First received
Last updated
Start date December 15, 2015
Est. completion date July 30, 2017

Study information

Verified date May 2019
Source Pontificia Universidad Catolica de Chile
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the effectiveness of a brief intervention for the reduction of alcohol use among risky alcohol users in primary care delivered by paramedics. Half of the participants will receive a brief intervention and half will receive written guidelines on safe alcohol use.


Description:

Randomized controlled trial with a pragmatic emphasis undertaken in real world primary care.

The brief intervention has been designed and piloted by the mental health team at the Chilean ministry of health, as also the written support material. This intervention is the same that is being implemented national wide.

The implementation will include training of the paramedics, and then an accreditation session with a simulated participant in a double sided mirror.

Randomization will take place on site using a opaque envelope. The sequence will be keep on site in a secured box.

Data will be registered by the same person delivering the intervention and kept safe at the clinical sites. Once a month the data will be physically transferred to the operational center at the San Joaquin site of the Catholic University of Chile.

Bimonthly visits will be performed to the centers by a member of the team to assure that the protocol is being followed and data audit.

The participants will receive an economical incentive for the follow up visit. Participants will be reached throw telephone at least twice to schedule that visit. If not possible, a telephonic outcome assessment or a domiciliary visit will be performed to minimize the lost in follow up.


Recruitment information / eligibility

Status Completed
Enrollment 342
Est. completion date July 30, 2017
Est. primary completion date July 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- AUDIT score between 8 and 15

- Able to read

- Haven't received a similar intervention in the last 3 months

Exclusion Criteria:

- Clients in treatment for alcohol use disorder

- Alcohol use treatment seekers

- Pregnant woman

- Severe physical or psychiatric pathology not stable

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
AUDIT brief intervention
Intervention will be provided following the Chilean ministry of health implementation manual on the AUDIT associated brief intervention. The pamphlet on alcohol use will be provided to participants.
Other:
Pamphlet on alcohol use
Only the pamphlet on alcohol use will be provided (the same received by participants on the intervention group). This is not an active intervention based on the current literature.

Locations

Country Name City State
Chile CESFAM Barros Luco Santiago San Miguel
Chile CESFAM Juan Pablo II Santiago Metropolitana
Chile CESFAM Madre Teresa de Calcuta Santiago Puente Alto
Chile CESFAM Recreo Santiago San Miguel
Chile CESFAM San Alberto Hurtado Santiago Puente Alto

Sponsors (1)

Lead Sponsor Collaborator
Pontificia Universidad Catolica de Chile

Country where clinical trial is conducted

Chile, 

Outcome

Type Measure Description Time frame Safety issue
Primary AUDIT score Total of questions 1 to 10 (minimum 0, maximum 40) 6 months post brief intervention
Secondary AUDIT-C score Total of questions 1 to 3 (minimum 0, maximum 12) 6 months post brief intervention
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