search
Back to results

PATH 2 Purpose: Primary Care and Community-Based Prevention of Mental Disorders in Adolescents (P2P)

Primary Purpose

Depression

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CATCH-IT
TEAMS
Sponsored by
University of Illinois at Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Depression focused on measuring Adolescents, Depression, Internet intervention, Cognitive-Behavioral Therapy, Prevention, Group Therapy

Eligibility Criteria

13 Years - 19 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adolescents ages 13 through 19 years, and
  • Adolescent must be experiencing an elevated level of depressive symptoms (Patient Health Questionnaire-9 Score = 5-18), and
  • Adolescent will be included if they have a past, but not current history of depression.

Exclusion Criteria:

  • Outside age range
  • A current diagnosis of Major Depression
  • Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) diagnosis of: schizophrenia, bipolar affective disorder, extreme current drug or alcohol abuse.
  • Currently using medication therapy for depression, anxiety, or other internalizing disorders for less than 3 months.
  • Currently engaged in individual treatment for a mood disorder
  • Currently engaged in a cognitive-behavioral group or therapy
  • Any past psychiatric hospitalizations
  • Any past self-harm attempt with moderate or greater lethality
  • Current suicidal thoughts
  • Not willing to comply with the study protocol
  • Not willing to participate in the TEAMS groups
  • Not willing to be audio recorded during TEAMS groups (only for TEAMS clinics)
  • Unable to complete the PHQ-9 screening due to cognitive or intellectual impairment
  • Did not complete phone assessment with MINI Kid
  • Parent/guardian has a cognitive or intellectual impairment.
  • Participant Declined/Changed Mind/Uninterested in participating

Sites / Locations

  • UI HealthRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CATCH-IT

TEAMS

Arm Description

Competent Adulthood Transition with Cognitive-behavioral & Interpersonal Training (CATCH-IT) is an internet-based depression prevention program that targets decreasing modifiable risk factors while enhancing protective factors in at-risk adolescents, and that includes a parent program. It has been shown to be safe, feasible, and efficacious.

Teens Achieving Mastery over Stress (TEAMS) is an 8-session group depression prevention program teaching teens how to deal with stress and negative moods, and ways to manage low mood based on cognitive-behavioral therapy (CBT) principles and strategies. Efficacy has been demonstrated by several trials over time.

Outcomes

Primary Outcome Measures

Time
Time will be measured to nearest minute for all intervention related activities including initial screening, engagement phone calls, use of CATCH-IT, TEAMS group activities, including travel time to and from TEAMS groups. Time will be measured from adolescent, family, practice, community center, healthcare organization, health system perspective. For time that cannot be directly measured by study staff, the investigators will sample direct observation or questionnaires to capture time required for health system related activities such as screening and engagement.
Cultural acceptability adolescent and family
Cultural acceptability for each stakeholder using appropriate, validated instruments. Adolescent and family: Usefulness, Satisfaction, and Ease Questionnaire (USE, 30 items, self-report, 7-point Likert scale, 30-210 score range, higher score indicates more acceptable). An example statement is: "I would recommend this to a friend."
Cost
Costs will be measured for all stakeholders. For practice, community center, healthcare organizations, health systems, cost will be measured to nearest dollar by converting time measures into employment related costs based on mean wages an benefits for staff at that occupational level. Adolescent and family costs will be measured by converting time into mean hourly wages and benefits for adolescent and family members involved in the project (based on mean wage for age and occupation).
Depressive and mental disorder episodes
Mini-International Neuropsychiatric Interview for Children and Adolescents (MINI Kid, self-report). This is a structured psychiatric interview administered by a trained staff member which uses stem questions and follow-ups to determine the presence of symptoms and date of onset. The staff member then determines if and when the symptoms developed an episode is present. Measure is either episode present or not and date of onset.
Stress symptoms
Center for Epidemiological Studies-Depression Scale (CES-D, 20 items, self-report, measured in frequency, 0,"not at all" to 3, "nearly every day in last week, 0-60 score range, higher score indicates more depressed)
Resiliency
Resiliency will be measured across multiple domains. To assess resiliency in terms of coping skills, the Connor-Davidson Resilience Scale (CD-RISC, 10 items, self-report, 4 levels of response, 0-40 score range, higher score indicates better coping skills)
Function
Social Adjustment Scale Self-Report (SAS-SR, 23-items, self-report, 5-point Likert scale, 23-115 score range, higher score indicates higher levels of social adjustment) administered to adolescents only.
Relationships (Life Events)
University of California at Los Angeles (UCLA) Life Events Scale (19-items, self-report) administered to adolescents only.
Socio-cultural Relevance
The Socio-Cultural Relevance Scale (10-item and 14-item versions, self-report, 5-point Likert scale, 10-40 or 14-56 score ranges, higher score indicates greater socio-cultural relevance) will assess perceived change and satisfaction with the intervention, component of cultural acceptability to adolescent)
Organizational Readiness to Change Assessment
Organizational Readiness to Change Assessment (ORCA, 18 questions, 4 items per question, self-report, 5-point Likert scale, 18-90 score range, higher score indicates higher organizational readiness, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Intervention Sustainability
Program Sustainability Assessment Tool (PSAT, 8 questions, self-report 5 items per question, 7-point Likert scale, 8-56 score range, higher score indicates higher capacity for program sustainability, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Acceptability of Intervention
Acceptability of Intervention Measure (AIM, 1 question with 4 items, self-report, 5-point Likert scale, 1-5 score range, higher score indicates greater acceptability of intervention, to be completed by all staff and leadership, repeatedly, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Feasibility of Intervention
Feasibility of Intervention Measure (FIM, 1 question with 4 items, self-report, 5-point Likert scale, 1-5 score range, higher score indicates greater feasibility of intervention, to be completed by all staff and leadership, repeatedly, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Intervention Appropriateness
Intervention Appropriateness Measure (IAM, 1 question with 4 items, self-report, 5-point Likert scale, 1-5 score range, higher score indicates greater appropriateness of intervention, to be completed by all staff and leadership, repeatedly, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Depressive Symptoms
Patient Health Questionnaire-Adolescent (PHQ-A, 9 items plus 4 follow-up items, self-report, 3-point Likert scale, 0-27 score range, higher score indicates more depression symptoms/severity)
Externalizing Behavior Symptoms
Disruptive Behavior Disorders Rating Scale-Adolescent (DBD-A, 41-items, self-report, 4-point Likert scale, 0-123 score range, higher score indicates greater externalizing symptoms)
Anxiety Symptoms
Screen for Child Anxiety Related Disorders (SCARED, 41-items, self-report, 3-point Likert scale, 0-82 score range, higher score indicates greater anxiety symptoms)
Substance Abuse Symptoms
Car, Relax, Alone, Forget, Friends, Trouble substance use assessment (CRAFFT, 6 items, self-report, 2-point scale, 0-6 score range, higher score indicates greater substance abuse symptoms)
Post Traumatic Stress Disorder Symptoms
Child Post Traumatic Symptoms Disorder Scale (24-items, self-report, 4-point Likert scale, 0-72 score range, higher score indicates greater PTSD symptom levels)
Rumination
Tendency towards rumination will be assessed by the Children's Response Style Scale (CRSS, 10-items, self-report, 5-point Likert scale, 0-50 score range, higher score indicates greater rumination (more repeated negative thinking, less resilient, component of resiliency)
Dysfunctional Attitudes
The Dysfunctional Attitude Scale (DAS, 9-item, self-report, 7-point Likert scale, 9-63 score range, higher score indicates more dysfunctional attitude, less resiliency, component of resiliency)
Relationships-Family
Child Report of Parental Behavior Inventory (CRPBI, 30-item, self-report, 3-point Likert scale, 0-60 score range, higher scores indicate more positive parent child relationship).
Blood Pressure
Measured in millimeters of mercury
Body Mass Index
Calculated by measuring height (centimeters) and weight (kilogram) to calculate kg/meters squared (BMI, Body Mass Index)
Weight
Measured in kilograms by standard medical office scale, fully clothed participant
Height
Measure by standard medical office practice measure, without shoes, in centimeters
Recruiting model and comparative effectiveness outcomes
With the addition of a second cohort to be recruited through a public health media campaign, we will compare results between groups in each arm, and between the two recruitment models. We will compare implementation and clinical outcomes in the same trial arm, but also across the two recruiting methods.

Secondary Outcome Measures

Implementation themes
Consolidated Framework for Implementation Research (CFIR) will be used to explore experience of the study from the perspective of 25 stakeholders
Moderation of Covid-19 factors on comparative effectiveness outcomes
We will examine factors related to the COVID-19 pandemic that may be moderators of study outcomes: (1) COVID-19-related behaviors and consequences (e.g. social distancing, sheltering-in-place, family illness and death), and (2) Social determinants of health (e.g. food insecurity, internet access, unemployment) in both cohorts using the Holliston at-Home Questionnaire (a 26-item, adolescent self-report, 5-point Likert scale, 0-150 score range, higher score indicates greater externalizing symptoms).

Full Information

First Posted
February 10, 2020
Last Updated
June 28, 2022
Sponsor
University of Illinois at Chicago
Collaborators
University of Illinois College of Medicine Rockford, Advocate Health Care, Katherine Shaw Bethea Hospital, University of Louisville, Wellesley College, Patient-Centered Outcomes Research Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT04290754
Brief Title
PATH 2 Purpose: Primary Care and Community-Based Prevention of Mental Disorders in Adolescents
Acronym
P2P
Official Title
PATH 2 Purpose: Primary Care and Community-Based Prevention of Mental Disorders in Adolescents
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
March 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Illinois at Chicago
Collaborators
University of Illinois College of Medicine Rockford, Advocate Health Care, Katherine Shaw Bethea Hospital, University of Louisville, Wellesley College, Patient-Centered Outcomes Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
PATH (Promoting AdolescenT Health) 2 Purpose is a two-arm comparative effectiveness research trial to that will evaluate the ability of the interventions, Competent Adulthood Transition with Cognitive-behavioral & Interpersonal Training (CATCH-IT) and Teens Achieving Mastery over Stress (TEAMS), to intervene early to prevent depressive illness and potentially other common mental health disorders. Using cluster randomization, 564 participants eligible for the study will be offered one of two different depression prevention programs in multiple sites in Chicagoland, Rockford, Illinois; Dixon, Illinois; and Louisville, Kentucky. In response to the Coronavirus Disease 2019 (COVID-19) pandemic, we will employ a public health media campaign to recruit a second cohort of 100 adolescents state-wide in Illinois, Kentucky, and Massachusetts individually randomized to either intervention. The study will also assess teens', parents' and providers' experiences with each intervention approach. Finally, we will examine the impact of the COVID-19 pandemic on adolescents at-risk for depression who are enrolled in our study.
Detailed Description
The majority of mental, emotional and behavioral (MEB) disorders have an initial onset before age 24, with 20% annual incidence, with major depressive disorder (MDD) being the most common MEB. Health systems, eager to reduce costs, want to transition from the current "wait until sick enough for treatment" model for MDD to a preventive model. However, evidence is needed for (1) the comparative effectiveness of a "scalable intervention" and (2) an implementation model for such a scalable intervention in the primary care setting. This study is a comparative effectiveness trial evaluating the efficacy of two evidence-based cognitive-behavioral prevention (CBP) programs: Teens Achieving Mastery over Stress (TEAMS), the "gold standard," group therapy model, and Competent Adulthood Transition with Cognitive Behavioral, Humanistic and Interpersonal Training (CATCH-IT), a scalable, self-directed, technology-based model. For implementation during the COVID-19 pandemic, TEAMS has successfully been adapted to an online format and administered online through HIPAA-compliant video conferencing software. For the first cohort, 564 eligible adolescents age 13-18 will be offered one of two different depression prevention programs using cluster randomization in multiple sites in urban and suburban Chicago, Illinois; rural Western Illinois, including Dixon and surrounding towns; and Louisville, Kentucky. Randomization will be blocked into matched pairs of primary health care clinics and school sites and stratified by race, ethnicity, rural-urban commuting area codes, and socio-economic disadvantage using the Distressed Communities Index (DCI) from census-tracked data of each site zip code. A second cohort of 100 eligible adolescents will be recruited through public health media campaigns in Illinois, Kentucky, and Massachusetts utilizing the same eligibility criteria as Cohort One. These participants will connect with the research team by phone, email, web survey, or social media and will be randomized at the individual-level with equal allocation into treatment conditions (CATCH-IT or TEAMS). The investigators will comprehensively evaluate patient-centered outcomes and stakeholder-valued moderators of effect at 2, 6, 12, and 18 month assessment points. Using a hybrid clinical trial design that simultaneously examines implementation process, the study will also assess adolescents', parents' and providers' experiences (i.e. efficacy, time commitment, cultural acceptability, and implementation cost) with each intervention approach. A sub-sample of Cohort Two (n=50, 25 from each intervention arm) will be recruited to participate in open-ended interviews for adolescents to share their experiences of living with subsyndromal depression, coping during the COVID-19 pandemic, their perceived impact of CATCH-IT or TEAMS on their mood and behavior, and the cultural contexts in which these experiences occurred.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
Keywords
Adolescents, Depression, Internet intervention, Cognitive-Behavioral Therapy, Prevention, Group Therapy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Comparative Effectiveness Study
Masking
ParticipantCare ProviderInvestigator
Masking Description
Cluster randomization of clinic sites
Allocation
Randomized
Enrollment
664 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CATCH-IT
Arm Type
Experimental
Arm Description
Competent Adulthood Transition with Cognitive-behavioral & Interpersonal Training (CATCH-IT) is an internet-based depression prevention program that targets decreasing modifiable risk factors while enhancing protective factors in at-risk adolescents, and that includes a parent program. It has been shown to be safe, feasible, and efficacious.
Arm Title
TEAMS
Arm Type
Active Comparator
Arm Description
Teens Achieving Mastery over Stress (TEAMS) is an 8-session group depression prevention program teaching teens how to deal with stress and negative moods, and ways to manage low mood based on cognitive-behavioral therapy (CBT) principles and strategies. Efficacy has been demonstrated by several trials over time.
Intervention Type
Behavioral
Intervention Name(s)
CATCH-IT
Intervention Description
Competent Adulthood Transition with Cognitive-behavioral & Interpersonal Training (CATCH-IT) is an internet-based depression prevention program that targets decreasing modifiable risk factors while enhancing protective factors in at-risk adolescents, and that includes a parent program. It has been shown to be safe, feasible, and efficacious.
Intervention Type
Behavioral
Intervention Name(s)
TEAMS
Other Intervention Name(s)
Prevention of Depression (POD)
Intervention Description
Teens Achieving Mastery over Stress (TEAMS) is an 8-session group depression prevention program teaching teens how to deal with stress and negative moods, and ways to manage low mood based on cognitive behavioral therapy (CBT) principles and strategies. Efficacy has been demonstrated by several trials over time.
Primary Outcome Measure Information:
Title
Time
Description
Time will be measured to nearest minute for all intervention related activities including initial screening, engagement phone calls, use of CATCH-IT, TEAMS group activities, including travel time to and from TEAMS groups. Time will be measured from adolescent, family, practice, community center, healthcare organization, health system perspective. For time that cannot be directly measured by study staff, the investigators will sample direct observation or questionnaires to capture time required for health system related activities such as screening and engagement.
Time Frame
Baseline through 18 months
Title
Cultural acceptability adolescent and family
Description
Cultural acceptability for each stakeholder using appropriate, validated instruments. Adolescent and family: Usefulness, Satisfaction, and Ease Questionnaire (USE, 30 items, self-report, 7-point Likert scale, 30-210 score range, higher score indicates more acceptable). An example statement is: "I would recommend this to a friend."
Time Frame
Baseline through 18 months
Title
Cost
Description
Costs will be measured for all stakeholders. For practice, community center, healthcare organizations, health systems, cost will be measured to nearest dollar by converting time measures into employment related costs based on mean wages an benefits for staff at that occupational level. Adolescent and family costs will be measured by converting time into mean hourly wages and benefits for adolescent and family members involved in the project (based on mean wage for age and occupation).
Time Frame
Baseline through 18 months
Title
Depressive and mental disorder episodes
Description
Mini-International Neuropsychiatric Interview for Children and Adolescents (MINI Kid, self-report). This is a structured psychiatric interview administered by a trained staff member which uses stem questions and follow-ups to determine the presence of symptoms and date of onset. The staff member then determines if and when the symptoms developed an episode is present. Measure is either episode present or not and date of onset.
Time Frame
Baseline through 18 months
Title
Stress symptoms
Description
Center for Epidemiological Studies-Depression Scale (CES-D, 20 items, self-report, measured in frequency, 0,"not at all" to 3, "nearly every day in last week, 0-60 score range, higher score indicates more depressed)
Time Frame
Baseline through 18 months
Title
Resiliency
Description
Resiliency will be measured across multiple domains. To assess resiliency in terms of coping skills, the Connor-Davidson Resilience Scale (CD-RISC, 10 items, self-report, 4 levels of response, 0-40 score range, higher score indicates better coping skills)
Time Frame
Baseline through 18 months
Title
Function
Description
Social Adjustment Scale Self-Report (SAS-SR, 23-items, self-report, 5-point Likert scale, 23-115 score range, higher score indicates higher levels of social adjustment) administered to adolescents only.
Time Frame
Baseline through 18 months
Title
Relationships (Life Events)
Description
University of California at Los Angeles (UCLA) Life Events Scale (19-items, self-report) administered to adolescents only.
Time Frame
Baseline through 18 months
Title
Socio-cultural Relevance
Description
The Socio-Cultural Relevance Scale (10-item and 14-item versions, self-report, 5-point Likert scale, 10-40 or 14-56 score ranges, higher score indicates greater socio-cultural relevance) will assess perceived change and satisfaction with the intervention, component of cultural acceptability to adolescent)
Time Frame
Baseline through 18 months
Title
Organizational Readiness to Change Assessment
Description
Organizational Readiness to Change Assessment (ORCA, 18 questions, 4 items per question, self-report, 5-point Likert scale, 18-90 score range, higher score indicates higher organizational readiness, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Time Frame
Baseline
Title
Intervention Sustainability
Description
Program Sustainability Assessment Tool (PSAT, 8 questions, self-report 5 items per question, 7-point Likert scale, 8-56 score range, higher score indicates higher capacity for program sustainability, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Time Frame
end of study, 30 months
Title
Acceptability of Intervention
Description
Acceptability of Intervention Measure (AIM, 1 question with 4 items, self-report, 5-point Likert scale, 1-5 score range, higher score indicates greater acceptability of intervention, to be completed by all staff and leadership, repeatedly, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Time Frame
end of study, 30 months
Title
Feasibility of Intervention
Description
Feasibility of Intervention Measure (FIM, 1 question with 4 items, self-report, 5-point Likert scale, 1-5 score range, higher score indicates greater feasibility of intervention, to be completed by all staff and leadership, repeatedly, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Time Frame
end of study, 30 months
Title
Intervention Appropriateness
Description
Intervention Appropriateness Measure (IAM, 1 question with 4 items, self-report, 5-point Likert scale, 1-5 score range, higher score indicates greater appropriateness of intervention, to be completed by all staff and leadership, repeatedly, component of cultural acceptability to practice, community center, healthcare organizations, health systems)
Time Frame
Baseline through 18 months
Title
Depressive Symptoms
Description
Patient Health Questionnaire-Adolescent (PHQ-A, 9 items plus 4 follow-up items, self-report, 3-point Likert scale, 0-27 score range, higher score indicates more depression symptoms/severity)
Time Frame
Baseline through 18 months
Title
Externalizing Behavior Symptoms
Description
Disruptive Behavior Disorders Rating Scale-Adolescent (DBD-A, 41-items, self-report, 4-point Likert scale, 0-123 score range, higher score indicates greater externalizing symptoms)
Time Frame
Baseline through 18 months
Title
Anxiety Symptoms
Description
Screen for Child Anxiety Related Disorders (SCARED, 41-items, self-report, 3-point Likert scale, 0-82 score range, higher score indicates greater anxiety symptoms)
Time Frame
Baseline through 18 months
Title
Substance Abuse Symptoms
Description
Car, Relax, Alone, Forget, Friends, Trouble substance use assessment (CRAFFT, 6 items, self-report, 2-point scale, 0-6 score range, higher score indicates greater substance abuse symptoms)
Time Frame
Baseline through 18 months
Title
Post Traumatic Stress Disorder Symptoms
Description
Child Post Traumatic Symptoms Disorder Scale (24-items, self-report, 4-point Likert scale, 0-72 score range, higher score indicates greater PTSD symptom levels)
Time Frame
Baseline through 18 months
Title
Rumination
Description
Tendency towards rumination will be assessed by the Children's Response Style Scale (CRSS, 10-items, self-report, 5-point Likert scale, 0-50 score range, higher score indicates greater rumination (more repeated negative thinking, less resilient, component of resiliency)
Time Frame
Baseline through 18 months
Title
Dysfunctional Attitudes
Description
The Dysfunctional Attitude Scale (DAS, 9-item, self-report, 7-point Likert scale, 9-63 score range, higher score indicates more dysfunctional attitude, less resiliency, component of resiliency)
Time Frame
Baseline through 18 months
Title
Relationships-Family
Description
Child Report of Parental Behavior Inventory (CRPBI, 30-item, self-report, 3-point Likert scale, 0-60 score range, higher scores indicate more positive parent child relationship).
Time Frame
Baseline through 18 months
Title
Blood Pressure
Description
Measured in millimeters of mercury
Time Frame
Baseline and 18 months
Title
Body Mass Index
Description
Calculated by measuring height (centimeters) and weight (kilogram) to calculate kg/meters squared (BMI, Body Mass Index)
Time Frame
Baseline and 18 months
Title
Weight
Description
Measured in kilograms by standard medical office scale, fully clothed participant
Time Frame
Baseline and 18 months
Title
Height
Description
Measure by standard medical office practice measure, without shoes, in centimeters
Time Frame
Baseline and 18 months
Title
Recruiting model and comparative effectiveness outcomes
Description
With the addition of a second cohort to be recruited through a public health media campaign, we will compare results between groups in each arm, and between the two recruitment models. We will compare implementation and clinical outcomes in the same trial arm, but also across the two recruiting methods.
Time Frame
Baseline through 18 months
Secondary Outcome Measure Information:
Title
Implementation themes
Description
Consolidated Framework for Implementation Research (CFIR) will be used to explore experience of the study from the perspective of 25 stakeholders
Time Frame
End of study, 30 months
Title
Moderation of Covid-19 factors on comparative effectiveness outcomes
Description
We will examine factors related to the COVID-19 pandemic that may be moderators of study outcomes: (1) COVID-19-related behaviors and consequences (e.g. social distancing, sheltering-in-place, family illness and death), and (2) Social determinants of health (e.g. food insecurity, internet access, unemployment) in both cohorts using the Holliston at-Home Questionnaire (a 26-item, adolescent self-report, 5-point Likert scale, 0-150 score range, higher score indicates greater externalizing symptoms).
Time Frame
Baseline through 18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adolescents ages 13 through 19 years, and Adolescent must be experiencing an elevated level of depressive symptoms (Patient Health Questionnaire-9 Score = 5-18), and Adolescent will be included if they have a past, but not current history of depression. Exclusion Criteria: Outside age range A current diagnosis of Major Depression Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) diagnosis of: schizophrenia, bipolar affective disorder, extreme current drug or alcohol abuse. Currently using medication therapy for depression, anxiety, or other internalizing disorders for less than 3 months. Currently engaged in individual treatment for a mood disorder Currently engaged in a cognitive-behavioral group or therapy Any past psychiatric hospitalizations Any past self-harm attempt with moderate or greater lethality Current suicidal thoughts Not willing to comply with the study protocol Not willing to participate in the TEAMS groups Not willing to be audio recorded during TEAMS groups (only for TEAMS clinics) Unable to complete the PHQ-9 screening due to cognitive or intellectual impairment Did not complete phone assessment with MINI Kid Parent/guardian has a cognitive or intellectual impairment. Participant Declined/Changed Mind/Uninterested in participating
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Benjamin W Van Voorhees, MD, MPH
Phone
312-996-8352
Email
bvanvoor@uic.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Matthew Lowther, MSW, MPH
Email
lowtherm@uic.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benjamin W Van Voorhees, MD, MPH
Organizational Affiliation
University of Illinois at Chicago, School of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tracy RG Gladstone, PhD
Organizational Affiliation
Wellesley College, Wellesley Centers for Women
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Matthew Lowther, MSW, MPH
Organizational Affiliation
University of Illinoist at Chicago
Official's Role
Study Director
Facility Information:
Facility Name
UI Health
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benjamin W Van Voorhees, MD, MPH
Email
bvanvoor@uic.edu
First Name & Middle Initial & Last Name & Degree
Rebecca Feinstein, PhD
Phone
13129962024
Email
rfeinst@uic.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://www.path2purpose.info/
Description
Path2Purpose Website

Learn more about this trial

PATH 2 Purpose: Primary Care and Community-Based Prevention of Mental Disorders in Adolescents

We'll reach out to this number within 24 hrs