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Clinical Trials/NCT05203198
NCT05203198
Active, not recruiting
Not Applicable

Primary Care Based Depression Prevention in Adolescents: Intervention Optimization in Preparation for Implementation Study

University of Illinois at Chicago6 sites in 1 country400 target enrollmentFebruary 1, 2022

Overview

Phase
Not Applicable
Intervention
Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training
Conditions
Depression
Sponsor
University of Illinois at Chicago
Enrollment
400
Locations
6
Primary Endpoint
Relationships (Life Events)
Status
Active, not recruiting
Last Updated
3 months ago

Overview

Brief Summary

Prevention of depressive disorders has become a key priority for the NIMH, but the investigators have no widely available public health strategy to reduce morbidity and mortality. To address this need, the investigators developed and evaluated the primary care based-technology "behavioral vaccine," Competent Adulthood Transition with Cognitive-Behavioral Humanistic and Interpersonal Therapy (CATCH-IT). The investigators will engage N=4 health systems representative of the United States health care system, and conduct a factorial design study to optimize the intervention in preparation for an implementation study and eventual dissemination.

Detailed Description

With more than 13% of adolescents diagnosed with depressive disorders each year, prevention of depressive disorders has become a key priority for the National Institute of Mental Health (NIMH). Unfortunately, the investigators have no widely available interventions to reduce morbidity and mortality (e.g. public health impact). To address this need, the investigators developed a multi-health system "collaboratory" to develop and evaluate the primary care based technology "behavioral vaccine," Competent Adulthood Transition with Cognitive-Behavioral Humanistic and Interpersonal Therapy (CATCH-IT) (14 adolescent, 5 parent modules). Using this health-system collaboratory model, the full CATCH-IT program (all modules), demonstrated evidence of efficacy in prevention of depressive episodes in phase-three clinical trials in the United States and China. However, like many "package" interventions, CATCH-IT became larger and more complex across efficacy trials. Thus, adolescents were less willing to complete all 14 modules, suggesting adolescent dose "tolerability" issues (e.g., satisfaction, acceptability and resource use, "time as cost"). Similarly, primary care practices have "scalability" challenges (acceptability, feasibility, resource use, cost), resulting in declining REACH (percent of at-risk youth who complete intervention). To prepare for implementation studies and dissemination, the investigators need to address adolescent tolerability and practice/health system scalability, while preserving efficacy. Multiphase Optimization Strategy (MOST) uses a systematic analytic approach and a factorial randomized clinical trial design to address efficacy, tolerability, and scalability, simultaneously. The investigators will use a MOST approach to optimize CATCH-IT for the prevention of depression (indicated prevention, i.e., elevated symptoms of depression) in practices and health systems representative of US geography and population. The theoretically grounded components of CATCH-IT selected for study and optimization include: behavioral activation, cognitive-behavioral therapy, interpersonal psychotherapy, and parent program. The investigators will use a 4-factor (2x2x2x2) fully crossed factorial design with N=16 cells (25 per cell, 15% dropout) to evaluate the contribution of each component. The investigators propose to randomize N=400 adolescents from multiple sites: Advocate-Aurora Health Care (n=200); Lurie Children's Hospital (n=70); NorthShore University HealthSystem (n=70); University of Chicago Comer Hospital (n=25); University of Texas (n=20); University of Illinois College of Medicine Peoria (n=15). The at-risk youth will be high school students 13 through 18 years old, not currently experiencing a mood disorder, but with subsyndromal symptoms of depression (moderate to high risk). Using the efficient factorial design, the investigators can assess the contribution to prevention efficacy of each component. Thus, the MOST study design will enable us to eliminate non-contributing components while preserving efficacy and to optimize CATCH-IT by strengthening tolerability and scalability by reducing "resource use." By reducing resource use, the investigators anticipate satisfaction and acceptability will also increase, preparing the way for an implementation trial and eventual US Preventive Services Task Force endorsement to support dissemination. Thus, the primary question is whether one component, or perhaps two, can demonstrate an equivalent effect to combinations of other components in terms of efficacy, whilst also demonstrating superior adolescent/family tolerability scalability over a 12-month follow-up.

Registry
clinicaltrials.gov
Start Date
February 1, 2022
End Date
October 31, 2026
Last Updated
3 months ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Benjamin Van Voorhees, MD, MPH

Professor and Head, Department of Pediatrics

University of Illinois at Chicago

Eligibility Criteria

Inclusion Criteria

  • Adolescents ages 13 through 18 years, and
  • Adolescents must be experiencing an elevated level of depressive symptoms (PHQ-9 = 5-18), and
  • Adolescents will be included if they have had past depressive episode/s, but not if they are in a current depressive episode.

Exclusion Criteria

  • Outside age range:
  • 12 or younger
  • 19 or older
  • Adolescent is a non-English speaker/reader
  • On the PHQ-9 screening, depression symptom level is:
  • PHQ-9 = 4 or lower
  • PHQ-9 =19 or higher
  • As assessed by the MINI Kid, a current depressive episode
  • As assessed by the MINI Kid, adolescent meets DSM-5 criteria for a psychotic or bipolar disorder.
  • Currently using medication therapy for depression, anxiety, or other internalizing disorders.

Arms & Interventions

10. Adolescent behavioral activation modules + parent program modules

Adolescent behavioral activation modules Parent program modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

11. Adolescent cognitive-behavioral therapy modules + parent program modules

Adolescent cognitive-behavioral therapy modules Parent program modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

12. Adolescent interpersonal therapy modules + parent program modules

Adolescent interpersonal therapy modules Parent Program

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

1. No adolescent modules + no parent modules

No adolescent nor parent modules will be offered to the participant.

2. Adolescent behavioral activation modules only

Adolescent behavioral activation modules only

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

3. Adolescent cognitive-behavioral therapy modules only

Adolescent cognitive-behavioral therapy modules only

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

4. Adolescent interpersonal therapy modules only

Adolescent interpersonal therapy modules only

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

5. Adolescent behavioral activation modules + cognitive-behavioral therapy modules

Adolescent behavioral activation modules Adolescent cognitive-behavioral therapy modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

6. Adolescent behavioral activation modules + interpersonal therapy modules

Adolescent behavioral activation modules Adolescent interpersonal therapy modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

7. Adolescent cognitive-behavioral therapy modules + interpersonal therapy modules

Adolescent cognitive-behavioral therapy modules Adolescent interpersonal therapy modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

8. Full Adolescent program only

Adolescent behavioral activation modules Adolescent cognitive-behavioral therapy modules Adolescent interpersonal therapy modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

9. Parent program modules only

Parent program modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

13. Adolescent behavioral activation + cognitive-behavioral therapy + parent program modules

Adolescent behavioral activation modules Adolescent cognitive-behavioral therapy modules Parent program modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

14. Adolescent behavioral activation + interpersonal therapy + parent program modules

Adolescent behavioral activation modules Adolescent interpersonal therapy modules Parent program modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

15. Adolescent cognitive-behavioral therapy + interpersonal therapy + parent program modules

Adolescent cognitive-behavioral therapy modules Adolescent interpersonal therapy modules Parent program modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

16. All adolescent + parent program modules

Adolescent behavioral activation modules Adolescent cognitive-behavioral therapy modules Adolescent interpersonal therapy modules Parent program modules

Intervention: Competent Adulthood Transition with Cognitive-Behavioral, Humanistic and Interpersonal Training

Outcomes

Primary Outcomes

Relationships (Life Events)

Time Frame: Baseline through 12 months

University of California at Los Angeles (UCLA) Life Events Scale (19-items, self-report) administered to adolescents only.

Time

Time Frame: Baseline through 12 months

Time will be measured to nearest minute for all intervention related activities including initial screening, engagement phone calls, use of CATCH-IT. 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.

Cost

Time Frame: Baseline through 12 months

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 and 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

Time Frame: Baseline through 12 months

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.

Cultural acceptability adolescent and family

Time Frame: Baseline through 12 months

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."

Stress symptoms

Time Frame: Baseline through 12 months

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).

Externalizing Behavior Symptoms

Time Frame: Baseline through 12 months

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).

Depressive Symptoms

Time Frame: Baseline through 12 months

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).

Function

Time Frame: Baseline through 12 months

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.

Feasibility of Intervention

Time Frame: Start to end of recruitment, 32 months

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).

Substance Abuse Symptoms

Time Frame: Baseline through 12 months

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).

Intervention Appropriateness

Time Frame: Start to end of recruitment, 32 months

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).

Anxiety Symptoms

Time Frame: Baseline through 12 months

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).

Cognitive Style

Time Frame: Baseline through 12 months

The Children's Cognitive Style Questionnaire (CCSQ, 6-items, self-report, 5-point Likert scale, 0-150 range, higher score indicates greater negativity of cognitive style).

Systolic and diastolic blood pressure

Time Frame: At baseline

Measured in millimeters of mercury.

Height

Time Frame: At baseline

Measure by standard medical office practice measure, without shoes, in centimeters.

Resiliency

Time Frame: Baseline through 12 months

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).

Post Traumatic Stress Disorder Symptoms

Time Frame: Baseline through 12 months

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).

Dysfunctional Attitudes

Time Frame: Baseline through 12 months

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).

Self-efficacy

Time Frame: Baseline through 12 months

The Trans-Theoretical Model Scale (TTMS, 10-item, self-report, 4-point Likert scale, 0-24 range, higher score indicates higher self-efficacy and intention to reduce depressive symptoms).

Weight

Time Frame: At baseline

Measured in kilograms by standard medical office scale, fully clothed participant.

Body Mass Index

Time Frame: At baseline

Calculated by measuring height (centimeters) and weight (kilogram) to calculate kg/meters squared (BMI, Body Mass Index).

Socio-cultural Relevance

Time Frame: Baseline through 12 months

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)

Acceptability of Intervention

Time Frame: Start to end of recruitment, 32 months

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).

Rumination

Time Frame: Baseline through 12 months

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).

Social Adjustment

Time Frame: Baseline through 12 months

The Social Adjustment Scale-Adolescent version (SAS-SR, 23-item, self-report, 5-point Likert scale, 0-115 range, higher score indicates higher level of social dysfunction).

Family Relationships

Time Frame: Baseline through 12 months

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).

Secondary Outcomes

  • Moderation of COVID-19-related social determinants of health(Baseline through 12 months)
  • Moderation of COVID-19-related behaviors and consequences(Baseline through 12 months)

Study Sites (6)

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