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Recruiting NCT07129070

Just-in-Time Training for Youth Mentors

No phase Interventional Mental Health Issue Depression Anxiety

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Interpersonal Psychotherapy-Adolescent Skills Training via Just-In-Time Training (JITT) implementation strategy, Interpersonal Psychotherapy-Adolescent Skills Training (IPT-AST) implemented via usual training.
Who it may be relevant to
Registry conditions: Mental Health Issue, Depression, Anxiety. Basic parameters: from 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Just-in-Time Training for Youth Mentors: A Strategy for Implementing Evidence-Based Preventive Interventions for Youth in Rural Communities

Overview

This study will evaluate the usability, feasibility, and acceptability of a novel multi-level Just-In-Time Training (JITT) implementation strategy (JITT-EBP) that aims to equip mentors and mentor supervisors to implement evidence-based practices (EBPs) with fidelity using methods that are sustainable in rural communities. JITT-EBP integrates (a) self-directed, on-demand, online training modules for mentors and mentor supervisors, (b) synchronous evidence-based supervision strategies, and (c) an apprenticeship delivery model in which EBPs are co-led by an experienced mentor and a novice mentor, providing opportunity for in-the-moment training and support. The study will conduct a pilot hybrid type 2 effectiveness-implementation trial to evaluate the use of JITT-EBP compared to usual training for implementing mentor-delivered Interpersonal Psychotherapy-Adolescent Skills Training (IPT-AST), an evidence-based depression prevention program. 96 adolescents (age 12-17) and their parents, 8-18 mentors (depending on amount of turnover), and 4 mentor supervisors will be enrolled in the trial.

Interventions

  • Behavioral Interpersonal Psychotherapy-Adolescent Skills Training via Just-In-Time Training (JITT) implementation strategy
    IPT-AST is a group-based EBP that aims to prevent depression and support emotional well-being by helping youth develop skills to foster healthy relationships. Youth learn about the links between feelings and interpersonal interactions, and they learn communication strategies and interpersonal problem-solving skills that they can apply to their relationships. JITT-EBP integrates (a) self-directed, on-demand, online training modules for mentors and mentor supervisors, (b) synchronous evidence-bas
  • Behavioral Interpersonal Psychotherapy-Adolescent Skills Training (IPT-AST) implemented via usual training
    IPT-AST is a group-based EBP that aims to prevent depression and support emotional well-being by helping youth develop skills to foster healthy relationships. Youth learn about the links between feelings and interpersonal interactions, and they learn communication strategies and interpersonal problem-solving skills that they can apply to their relationships. Usual training involves (a) a one-day virtual training conducted by an IPT-AST expert prior to the beginning of the intervention, and (b)

Primary outcome measures

  • Feasibility of Intervention Measure (FIM) - Week 12 [Time frame: Week 12]
  • Acceptability of Intervention Measure (AIM) - Week 12 [Time frame: Week 12]
  • Intervention Appropriateness Measure (IAM) - Week 12 [Time frame: Week 12]
  • Client Satisfaction Questionnaire (CSQ-8) - Week 12 [Time frame: Week 12]
Secondary outcome measures (12)
  • Fidelity [Time frame: Week 12]
  • Cost of implementation [Time frame: Year 2]
  • Revised Child Anxiety and Depression Scale-25 (RCADS-25) - Week 6 [Time frame: Week 6]
  • Revised Child Anxiety and Depression Scale-25 (RCADS-25) - Week 12 [Time frame: Week 12]
  • Revised Child Anxiety and Depression Scale-25 (RCADS-25) - Week 24 [Time frame: Week 24]
  • Conflict Behavior Questionnaire-20 (CBQ-20) - Week 6 [Time frame: Week 6]
  • Conflict Behavior Questionnaire-20 (CBQ-20) - Week 12 [Time frame: Week 12]
  • Conflict Behavior Questionnaire-20 (CBQ-20) - Week 24 [Time frame: Week 24]
  • National Survey of Children's Health Social Competence Scale (NSCH-SCS) - Week 6 [Time frame: Week 6]
  • National Survey of Children's Health Social Competence Scale (NSCH-SCS) - Week 12 [Time frame: Week 12]
  • National Survey of Children's Health Social Competence Scale (NSCH-SCS) - Week 24 [Time frame: Week 24]
  • NIH Toolbox -Loneliness Ages 8-17 - Week 6 [Time frame: Week 6]

Eligibility criteria

Youth and Parent Inclusion Criteria:

  • student at a partnering rural middle school or high school
  • age 12-17
  • have English speaking/reading/writing ability at a level to participate in IPT-AST
  • youth's parent has English or Spanish-speaking/reading/writing ability at a level to participate in research activities.

Youth and Parent Exclusion Criteria:

  • moderate or severe depression (PHQ-9 > 10)
  • active suicidal ideation with a plan and/or intent, requiring higher level of care
  • Youth does not have English-speaking ability at a level to participate in IPT-AST
  • youth's parent does not have English or Spanish-speaking/reading/writing ability at a level to participate in research activities.

Mentor and Mentor Supervisor Inclusion Criteria:

  • age 18 or older
  • have completed the typical mentor or mentor supervisor screening and selection process at partnering mentoring organization (including a background check)
  • are available to facilitate the program during after-school hours.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

United States · 1 center
  • University of Minnesota — Minneapolis

Identifiers

NCT: NCT07129070 · STUDY00024848

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗