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Mentoring Program for Mental Health (SMART Trial)
N/A
Recruiting
Led By David DuBois, PhD
Research Sponsored by University of Illinois at Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Youth is between 9- and 16-years-old
Be younger than 18 years old
Must not have
Youth difficulties in cognitive functioning that would preclude ability to complete study assessments
Timeline
Screening 3 weeks
Treatment Varies
Follow Up end of study participation, average of 2 years
Awards & highlights
No Placebo-Only Group
Summary
"This trial aims to see if participating in the Great Life Mentoring (GLM) program can improve the mental health and adaptive functioning of school-age youth from low-income families who are already receiving mental health
Who is the study for?
This trial is for school-age youth, ages 9-16, from low-income families who are currently receiving outpatient mental health services. To participate, they must have consent from their parent or guardian and agree to annual surveys as well as sharing their mental health service records.
What is being tested?
The study is testing the Great Life Mentoring (GLM) program's impact on improving mental health and adaptive functioning in youths. Participants will either continue with standard outpatient services (SAU) or receive SAU plus GLM. The two groups' outcomes will be compared over time.
What are the potential side effects?
Since this trial involves a mentoring program rather than medication, traditional physical side effects are not expected. However, participants may experience changes in mood or behavior due to the nature of the intervention.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 9 and 16 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not have cognitive difficulties that prevent me from completing study tasks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ end of study participation, average of 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~end of study participation, average of 2 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Anxiety Symptoms
Depressive Symptoms
Externalizing Symptoms
+8 moreSecondary study objectives
Academic Success
Adaptive Coping with Stress
Career Exploration
+30 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: GLM + Services as UsualExperimental Treatment1 Intervention
The Great Life Mentoring program (GLM) provides volunteer-based mentoring for school-age youth from low-resource families who are receiving outpatient mental health care. Each youth is paired with a mentor with whom they spend time in the community on a weekly basis for at least one year. Mentors are required to complete a 20-hour intensive training prior to being paired with a youth. Mentors also receive monthly in-person supervision from GLM staff for the first year of their meetings, which continues on an as-needed basis thereafter. Training and supervision are geared toward the unique opportunities and challenges that can occur when mentoring a youth with mental health needs. The goal is for the mentor to become an integral part of the child's mental health treatment, but the mentoring relationship is also sustained after treatment ends.
Group II: Services as UsualActive Control1 Intervention
Outpatient mental health services as usual
Find a Location
Who is running the clinical trial?
Herrera Consulting Group, LLCUNKNOWN
2 Previous Clinical Trials
2,161 Total Patients Enrolled
University of Illinois at ChicagoLead Sponsor
639 Previous Clinical Trials
1,568,974 Total Patients Enrolled
1 Trials studying Mental Health
300 Patients Enrolled for Mental Health
David DuBois, PhDPrincipal InvestigatorUniversity of Illinois Chicago
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