Randomized Controlled Trial of Big Brothers Big Sisters Mentoring for Prevention of Crime and Delinquency

March 4, 2024 updated by: David DuBois, University of Illinois at Chicago

Randomized Controlled Trial of the Big Brothers Big Sisters Community-Based Mentoring Program for Prevention of Crime and Juvenile Delinquency

The purpose of this study is to evaluate the effectiveness of the Big Brothers Big Sisters of America (BBBSA) community-based mentoring (CBM) program for prevention of crime and delinquency/conduct problems, including risk and protective factors for these outcomes. Approximately 2,500 youth ages 10-16 will be randomly assigned to either the CBM program or an untreated control group. Study outcomes will be assessed over a 4-year period via both youth- and parent-report surveys and official records of police/court contact (e.g., arrests).

Study Overview

Status

Active, not recruiting

Detailed Description

The purpose of this study is to evaluate the effectiveness of the Big Brothers Big Sisters of America (BBBSA) community-based mentoring (CBM) program for prevention of crime and delinquency/conduct problems, including risk and protective factors for these outcomes. Participants will be recruited from 16 BBBSA affiliates, which are located in different regions of the U.S. and were invited to serve as sites for the study using a random selection process. The study sample will consist of approximately 2,500 youth ages 10-16 whose parents seek services from one of the participating BBBSA affiliates during the study enrollment period and for whom consent/assent to participate in the research is obtained. Enrolled youth will be randomly assigned to participate in the CBM program (treatment group) or to a control group (no BBBSA programming during the youth's 4-year period of study participation). Youth will be assigned in a 3:1 ratio to the treatment and control groups. Youth and parents will complete survey measures both at study enrollment, prior to notification of assignment to control or treatment group, and 18 months later. Official records of police/court contact (e.g., arrests), with separate parent/guardian consent as provided at study enrollment, will be obtained both for the period preceding each youth's enrollment in the study and for a 4-year period following enrollment.

The study has 4 specific aims:

  1. To determine the effects of participation in the Big Brothers Big Sisters CBM program on youth offending as measured by police/court records, i.e., person offense, property offense, drug law violation, public order offense, or status offense.
  2. To determine the effects of participation in the BBBS CBM program on the likelihood of youths' involvement in delinquent behavior/conduct problems as assessed by youth and parent reports.
  3. To determine the effects of BBBS CBM program participation on the likelihood of youths' involvement in substance use as assessed by self-reports of alcohol use to point of drunkenness, tobacco, or illicit drug use.
  4. To determine the effects of BBBS CBM program participation on both risk and protective factors for delinquent/criminal behavior, such as aggression, depressive symptoms, association with deviant peers, self-control, and school connectedness, as assessed by youth and/or parent reports, and to explore the role of these effects in mediating effects of program participation on offending, delinquent behavior, and substance use.

Study Type

Interventional

Enrollment (Actual)

1361

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Chicago, Illinois, United States, 60608
        • University of Illinois at Chicago

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

10 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria:

  • youth is 10 years of age or older
  • youth is likely to be eligible for the Big Brothers Big Sisters Community-Based Mentoring program as determined by initial assessment of program staff

Exclusion criteria:

  • youth has a severe learning, cognitive or other intellectual disability as reported by the parent
  • parent does not both speak and read either English or Spanish
  • youth does not have a sibling who is already a study participant
  • youth has been matched with a Big Brother/Sister through one of the affiliate's programs in the past
  • youth has a sibling currently receiving services from the affiliate for whom services were initiated (i.e., inquiry was made) prior to start of the study
  • youth belongs to a group that the affiliate is excluding from study participation based on previous agreement with the research team
  • youth is designated as an exception case by affiliate staff (each affiliate will have the opportunity to exclude up to 4% of study-eligible youth from the research prior to consent and random assignment for any reason deemed appropriate (e.g., perceived high need of the youth))

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: BBBS Community-Based Mentoring
Big Brothers Big Sisters Community-Based Mentoring Program
One-to-one mentoring provided by an adult volunteer with training and ongoing monitoring and support from program staff.
No Intervention: Control
Not eligible to participate in a Big Brothers Big Sisters mentoring program, but may participate in other mentoring programs.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Arrest
Time Frame: 4 years
0/1 indicator based on official police/court/juvenile office records of any of the following types of offenses-person offense, property offense, drug law violation, public order offense, or status offense
4 years
Arrest
Time Frame: 18 months
0/1 indicator based on official police/court/juvenile office records of any of the following types of offenses-person offense, property offense, drug law violation, public order offense, or status offense
18 months
Delinquency
Time Frame: 18 months
0/1 indicator based on youth and parent report using 13 items from the Add Health Study (Bearman et al., 1997)
18 months
Substance use
Time Frame: 18 months
0/1 indicator based on youth report of alcohol use to point of drunkenness, tobacco, or illicit drug use
18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Truancy
Time Frame: 18 months
3-item youth-report measure (2 items from Herrera et al., 2013)
18 months
Association with deviant peers
Time Frame: 18 months
A single measure computed as the average of scores on continuous youth-report measure (Elliott et al., 1996) and one-item (0/1) parent-report indicator from Youth Risk Index (Herrera et al., 2013) after each score has been standardized to mean of 0 and standard deviation of 1.
18 months
School suspensions
Time Frame: 18 months
One-item (0/1) parent-report indicator from Youth Risk Index (Herrera et al., 2013)
18 months
Depressive symptoms
Time Frame: 18 months
Depressive Symptoms Pediatric Self-Report - Short Form from the Patient-Reported Outcomes Measurement Information System (PROMIS) (Irwin et al., 2010). Lower scores indicate a better outcome
18 months
Impulsivity
Time Frame: 18 months
A single measure computed as the average of scores on continuous youth- and parent-report scales (Hay & Meldrum, 2010) after each score has been standardized to mean of 0 and standard deviation of 1.
18 months
Conventional values
Time Frame: 18 months
Belief in the Moral Order scale of the Communities That Care Youth Survey (Arthur et al., 2002)
18 months
Aggressive behavior
Time Frame: 18 months
A single measure computed as the average of scores on youth-report Aggression Scale (Orpinas & Frankowski, 2001) and parent-report Parent's Checklist from the Fast Track Project: https://fasttrackproject.org/techrept/p/pcl/ after each score has been standardized to mean of 0 and standard deviation of 1.
18 months
Academic success
Time Frame: 18 months
4-item measure of grades in core subjects (Herrera et al., 2013)
18 months
Positive parenting
Time Frame: 18 months
Parent-report Positive Parenting subscale from the Alabama Parenting Questionnaire (Essau et al., 2006)
18 months
Parent involvement
Time Frame: 18 months
Parent-report Involvement subscale from the Alabama Parenting Questionnaire (Essau et al., 2006)
18 months
Parental monitoring and supervision
Time Frame: 18 months
Parent-report Poor Monitoring/Supervision subscale from the Alabama Parenting Questionnaire (Essau et al., 2006)
18 months
Parental consistent discipline
Time Frame: 18 months
Parent-report Inconsistent Discipline subscale from the Alabama Parenting Questionnaire (Essau et al., 2006)
18 months
Family relationships
Time Frame: 18 months
Parent-report General Functioning scale of the Family Assessment Device (Epstein et al., 1983)
18 months
Perceived social support from family members
Time Frame: 18 months
Youth-report Multidimensional Scale of Perceived Social Support (Zimet et al., 1988): Family Members subscale
18 months
Perceived social support from peers
Time Frame: 18 months
Youth-report Multidimensional Scale of Perceived Social Support (Zimet et al., 1988): Peers subscale
18 months
Perceived social support from special person
Time Frame: 18 months
Youth-report Multidimensional Scale of Perceived Social Support (Zimet et al., 1988): Significant Others subscale
18 months
School engagement
Time Frame: 18 months
Youth-report Behavioral Engagement subscale of the Engagement versus Disaffection with Learning Scale (Skinner et al., 2009)
18 months
Goal-setting and pursuit
Time Frame: 18 months
Parent-report Goal Orientation scale from Child Trends: https://www.childtrends.org/research/research-by-topic/positive-indicators-project/goal-orientation/
18 months
Involvement in out-of-school-time activities
Time Frame: 18 months
Parent-report (Herrera et al., 2007)
18 months
Volunteering in the community
Time Frame: 18 months
Youth-report single-item (Herrera et al., 2013)
18 months
Life satisfaction
Time Frame: 18 months
Youth-report single-item measure from WHO's 2005-06 Health Behaviors in School Age Children Survey: http://filer.uib.no/psyfa/HEMIL-senteret/HBSC/2006_Mandatory_Questionnaire.pdf
18 months
Self-esteem
Time Frame: 18 months
Youth-report Global Self-Esteem subscale of brief version of the Self-Esteem Questionnaire (DuBois et al., 1996; Silverthorn et al., 2017)
18 months
Happiness
Time Frame: 18 months
Youth-report Positive Affect Pediatric Self-Report - Short Form from the Patient-Reported Outcomes Measurement Information System (PROMIS) (Forrest et al., 2017)
18 months
Grit
Time Frame: 18 months
Youth-report Grit Scale for Children (Duckworth & Quinn, 2009)
18 months
Social competence
Time Frame: 18 months
Social Competencies Scale of the Youth Outcome Measures Online Toolbox (Muris, 2001)
18 months
Special interest development
Time Frame: 18 months
Youth-report (adapted from DuBois & Keller, 2017)
18 months
Hopeful future expectations
Time Frame: 18 months
Youth-report abbreviated version of the Hopeful Future Expectations Scale (Bowers et al., 2012)
18 months
Career exploration
Time Frame: 18 months
Youth-report 2 items (adapted from Herrera et al., 2011)
18 months
College exploration
Time Frame: 18 months
Youth-report 1 item (adapted from Herrera et al., 2011)
18 months
Self-advocacy
Time Frame: 18 months
Youth-report (Jarjoura et al., 2017)
18 months
Coping efficacy
Time Frame: 18 months
Youth-report 1 item adapted from Coping Efficacy Scale (Sandler et al., 2000)
18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: David L DuBois, PhD, University of Illinois at Chicago
  • Principal Investigator: Carla Herrera, PhD, Herrera Consulting Group, LLC

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 2, 2018

Primary Completion (Estimated)

June 30, 2024

Study Completion (Estimated)

June 30, 2024

Study Registration Dates

First Submitted

January 4, 2018

First Submitted That Met QC Criteria

April 4, 2018

First Posted (Actual)

April 12, 2018

Study Record Updates

Last Update Posted (Estimated)

March 6, 2024

Last Update Submitted That Met QC Criteria

March 4, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2017-0291

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

At the study's conclusion, all individual participant data will be de-identified and made publicly available on the Open Science Framework website along with survey instruments and any code used to clean and analyze the data.

IPD Sharing Time Frame

Data will become available August 2024 and will be permanently available thereafter

IPD Sharing Access Criteria

Requests to access the IPD will be made in writing to the Principal Investigator and approved so long as there is a valid scientific rationale and appropriate IRB approval. The mechanism for sharing the data, all of which will be de-identified, will be secure and encrypted FTP and subject to approval of the PI's institutional IRB. Supporting information (see above list) will be available on the Open Science Framework at the web address below.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE

Study Data/Documents

  1. Individual Participant Data Set
    Information identifier: osf.io/8ukfv

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Juvenile Delinquency

Clinical Trials on Big Brothers Big Sisters Community-Based Mentoring Program

  • University of Illinois at Chicago
    National Institute of Mental Health (NIMH); Big Brothers Big Sisters of Metropolitan...
    Completed
    Self Concept
    United States
3
Subscribe