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Impact of Personalized Feedback Alone on Substance Use Behaviors

Brief Education to Reduce Health Care Consumers' Risky Substance Use Behaviors: How Brief is Brief?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01501318
Enrollment
40
Registered
2011-12-29
Start date
2012-02-29
Completion date
2012-11-30
Last updated
2016-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance Abuse

Keywords

SBIRT, brief intervention, alcohol, drug abuse

Brief summary

The investigators seek to develop a more efficient and effective approach to providing brief behavioral health interventions for risky substance use behaviors by comparing a brief coach directed intervention to a tailored report only group.

Detailed description

Screening and brief intervention (SBIRT) generally involves universal screening for risky substance use behaviors in medical settings and the immediate provision of a 3-15 minute intervention to those found to be at risk. In this pilot study, the investigators seek to develop a more efficient and effective approach to providing brief behavioral health interventions in the field by comparing a brief coach directed intervention to a tailored report only group. The goal is to create a cost-effective and sustainable system that provides consumers with tailored information that will help them both initiate and sustain the lifestyle changes necessary for improving their overall health. Hypothesis 1: In a medical setting, personalized feedback alone will be associated with a reduction in risky substance use behaviors. Hypothesis 2: In a medical setting, personalized feedback alone will have the same impact on behavior as that information plus a brief coach education session on risky substance use behaviors..

Interventions

Participants receive the personalized feedback report but no additional education.

BEHAVIORALPersonalized feedback report plus education

Participants receive the personalized feedback report plus education. This is the currently implemented service approach.

Sponsors

University of Missouri, St. Louis
CollaboratorOTHER
Institute of Mental Health, Singapore
CollaboratorOTHER
University of Missouri-Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 105 Years
Healthy volunteers
No

Inclusion criteria

* Low level risky substance use

Exclusion criteria

* high substance use risk levels * potential alcohol or drug addiction or dependence

Design outcomes

Primary

MeasureTime frameDescription
Substance use behaviors and consequences1 month follow-upInterview questionnaire includes items concerning substance use behaviors (e.g., the number of drinks in the last 7 days) and consequences {e.g., ''During the past month, how often have you failed to do what was normally expected of you because of your use of alcohol?'

Secondary

MeasureTime frameDescription
Substance use behavioral intentions1 month follow-upInterview questionnaire that asks participants about their memory of the materials provided in the intervention, their motivation toward change, and their self-reported change efforts.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026