NCT03059433

Brief Summary

Advancement via Individual Determination (AVID) is a college preparatory program that provides a unique opportunity to determine whether schools can reduce substance use by re-grouping at-risk students with high-performing students, while providing additional academic and emotional support. Operating in 4,837 K-12th grade schools worldwide and across 45 US states, this widely-disseminated program targets students from groups traditionally underrepresented in higher education who are currently performing in the academic middle (i.e., a 2.0-3.5 grade point average). AVID removes these students from typical classrooms and exposes them to a peer network in which academic performance and positive social norms are valued. In addition, by strengthening the student/teacher relationship, AVID expands students' networks of supportive adults. For low-income minority students in the academic middle, relatively small investments in prevention might significantly impact their academic and health trajectories. AVID capitalizes on a moment when social networks are in flux-the transition to high school-to shift these students' trajectories. This study is a longitudinal, randomized pilot evaluation of AVID among low-income minority adolescents entering high school, comparing academic performance and drug use, as well as other risky behaviors, over 3 years. Although social networks are hypothesized to have a strong influence on behavior, few studies have tried to re-wire networks to change behaviors. This study will provide a clearer understanding of whether schools can intentionally shape networks and whether these changes can reduce substance use. This study will also explore important mechanistic questions about whether and how AVID changes peer networks and relationships with teachers, whether those changes lead to improvements in academic and behavioral outcomes and, if so, what the relative importance of peer versus adult network changes are.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
446

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2017

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 13, 2017

Completed
10 days until next milestone

First Posted

Study publicly available on registry

February 23, 2017

Completed
2 months until next milestone

Study Start

First participant enrolled

April 21, 2017

Completed
4.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 2, 2021

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

July 6, 2022

Completed
Last Updated

October 3, 2022

Status Verified

September 1, 2022

Enrollment Period

4.2 years

First QC Date

February 13, 2017

Last Update Submit

September 30, 2022

Conditions

Keywords

Substance useadolescenthealthsocial network

Outcome Measures

Primary Outcomes (1)

  • Change in health of social network

    Investigators will evaluate whether students randomized to AVID report healthier social networks (lower proportion of peers engaging in risky behaviors and a higher number of supportive adults) than control students.

    change in health of social network between baseline and 3 year follow up

Secondary Outcomes (3)

  • Frequency of risky health behaviors

    change in frequency of risky health behaviors between baseline and 3 year follow up

  • Change in peer or adult social network

    change in risky behavior between baseline and 3 year follow up

  • Assumptions of AVID students' level of their own risky health behaviors

    change in student assumption of risky behavior between baseline and 3 year follow up

Study Arms (3)

AVID Intervention

175 students will be randomized via lottery by the participating high school to be part of the AVID program. These students will receive 4 surveys (8th, 9th, 10th, and 11th grade).

Other: AVID Intervention

Non AVID

175 students will be randomized via lottery by the participating high school to be part of our control group. This group of students will be similar to the AVID group, except they will not be in the AVID program. They will also complete 4 surveys (8th, 9th, 10th, and 11th grade).

High Performing

175 students who are identified as high performing (middle school grade point average \>3.5) by the participating high school. They will also complete 4 surveys (8th, 9th, 10th, and 11th grade).

Interventions

Advancement via Individual Determination (AVID) is a college preparatory program that participating high schools have available to students.

Also known as: AVID
AVID Intervention

Eligibility Criteria

Age13 Years - 18 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Participants must be eighth grade students who are entering a Los Angeles Unified School District high school that is having a lottery for admission into their AVID program.

You may qualify if:

  • applied to and was deemed eligible for AVID by the AVID coordinator
  • Student participated in the AVID lottery
  • Parent consents to participate in study
  • Student assents to participate in study
  • Middle school Grade Point Average (GPA) \>3.5
  • Planning to attend study high school
  • Parent consents to participate in study
  • Student assents to participate in study

You may not qualify if:

  • Student did not apply to AVID
  • Student was deemed ineligible for AVID by the AVID coordinator/local AVID admissions process
  • Student did not participate in the AVID lottery
  • Parent does not consent for study participation
  • Student does not assent for study participation
  • Middle school Grade Point Average (GPA)\<3.5
  • Not planning to attend study high school
  • Parent does not consent for study participation
  • Student does not assent for study participation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of California, Los Angeles (UCLA)

Los Angeles, California, 90095, United States

Location

MeSH Terms

Conditions

Adolescent BehaviorSubstance-Related Disorders

Condition Hierarchy (Ancestors)

BehaviorChemically-Induced DisordersMental Disorders

Study Officials

  • Rebecca Dudovitz, MD, MS

    University of California, Los Angeles

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 13, 2017

First Posted

February 23, 2017

Study Start

April 21, 2017

Primary Completion

July 2, 2021

Study Completion

July 6, 2022

Last Updated

October 3, 2022

Record last verified: 2022-09

Data Sharing

IPD Sharing
Will not share

Participants will be assigned a study ID number to link their name, address, and phone number to their survey responses. This ID will be used for all data collection. The computer file linking the personal identifiers and the study ID number will be kept separate from the survey data. Personally identifying information pertaining to individual participants will not be shared or made available to other researchers. Any data request will be made to the Principal Investigator and any data shared will be encrypted and will not include any personal identifying information.

Locations