CClinicalTrials.gg
RecruitingNCT07129070Updated Apr 24, 2026

Just-in-Time Training for Youth Mentors

An interventional study of Interpersonal Psychotherapy-Adolescent Skills Training via Just-In-Time Training (JITT) implementation strategy and Interpersonal Psychotherapy-Adolescent Skills Training (IPT-AST) implemented via usual training in Mental Health Issue, Depression and Anxiety, sponsored by University of Minnesota. Recruiting at 1 site in United States. Open to participants aged 12 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-24.

Sponsored by University of Minnesota · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started Dec 2025; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
204
Allocation
Randomized
Ages
12 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Mental Health Issue
  • Depression
  • Anxiety
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's planned enrollment of 204 is above the median of 84 across 6,720 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

University of Minnesota is the lead sponsor of 1,184 studies on the registry; 195 are open to participants now.

Of its 132 completed or terminated interventional studies of FDA-regulated products, 91 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
204 participants (estimated)

Study arms

  • Active comparator
    IPT-AST implemented via Just-In-Time Training (JITT-EBP)

    IPT-AST = Interpersonal Psychotherapy-Adolescent Skills Training

    Behavioral: Interpersonal Psychotherapy-Adolescent Skills Training via Just-In-Time Training (JITT) implementation strategy

  • Active comparator
    IPT-AST implemented via usual training

    IPT-AST = Interpersonal Psychotherapy-Adolescent Skills Training

    Behavioral: Interpersonal Psychotherapy-Adolescent Skills Training (IPT-AST) implemented via usual training

Interventions

  • BehavioralInterpersonal 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-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.

  • BehavioralInterpersonal 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) synchronous evidence-based supervision strategies.

06

What researchers measure

Primary outcomes

  1. Feasibility of Intervention Measure (FIM) - Week 12

    Mentor and mentor supervisor report of JITT-EBP feasibility, with higher value indicating higher feasibility

    Time frame: Week 12

  2. Acceptability of Intervention Measure (AIM) - Week 12

    youth, parent, mentor, and mentor supervisor report of IPT-AST acceptability, with higher value indicating higher acceptability.

    Time frame: Week 12

  3. Intervention Appropriateness Measure (IAM) - Week 12

    Mentor and mentor supervisor report of JITT-EBP appropriateness, with higher value indicating higher appropriateness.

    Time frame: Week 12

  4. Client Satisfaction Questionnaire (CSQ-8) - Week 12

    Youth and parent report of satisfaction with IPT-AST program, with , with higher value indicating more satisfaction.

    Time frame: Week 12

Secondary outcomes

  1. Fidelity

    IPT-AST fidelity checklist

    Time frame: Week 12

  2. Cost of implementation

    Mentor Supervisor hours and hourly wages for recruitment, training, supervision, and IPT-AST delivery. IPT-AST expert hours and hourly wages for training and supervision.

    Time frame: Year 2

  3. Revised Child Anxiety and Depression Scale-25 (RCADS-25) - Week 6

    25-item scale that measures levels of anxiety and depressed mood. Higher scores indicate higher severity.

    Time frame: Week 6

  4. Revised Child Anxiety and Depression Scale-25 (RCADS-25) - Week 12

    25-item scale that measures levels of anxiety and depressed mood. Higher scores indicate higher severity.

    Time frame: Week 12

  5. Revised Child Anxiety and Depression Scale-25 (RCADS-25) - Week 24

    25-item scale that measures levels of anxiety and depressed mood. Higher scores indicate higher severity.

    Time frame: Week 24

  6. Conflict Behavior Questionnaire-20 (CBQ-20) - Week 6

    A higher score on the CBQ-20 indicates a greater level of conflict in parent-adolescent relationships

    Time frame: Week 6

  7. Conflict Behavior Questionnaire-20 (CBQ-20) - Week 12

    A higher score on the CBQ-20 indicates a greater level of conflict in parent-adolescent relationships

    Time frame: Week 12

  8. Conflict Behavior Questionnaire-20 (CBQ-20) - Week 24

    A higher score on the CBQ-20 indicates a greater level of conflict in parent-adolescent relationships

    Time frame: Week 24

  9. National Survey of Children's Health Social Competence Scale (NSCH-SCS) - Week 6

    A higher score on the NSCH-SCS indicates a higher level of youth social skills, as reported by a parent.

    Time frame: Week 6

  10. National Survey of Children's Health Social Competence Scale (NSCH-SCS) - Week 12

    A higher score on the NSCH-SCS indicates a higher level of youth social skills, as reported by a parent.

    Time frame: Week 12

  11. National Survey of Children's Health Social Competence Scale (NSCH-SCS) - Week 24

    A higher score on the NSCH-SCS indicates a higher level of youth social skills, as reported by a parent.

    Time frame: Week 24

  12. NIH Toolbox -Loneliness Ages 8-17 - Week 6

    A higher score indicates greater severity of loneliness

    Time frame: Week 6

  13. NIH Toolbox -Loneliness Ages 8-17 - Week 12

    A higher score indicates greater severity of loneliness

    Time frame: Week 12

  14. NIH Toolbox -Loneliness Ages 8-17 - Week 24

    A higher score indicates greater severity of loneliness

    Time frame: Week 24

  15. PROMIS Pediatric Item Bank - Peer Relationships - Week 6

    A higher score indicates a more positive experience in relationships with peers

    Time frame: Week 6

  16. PROMIS Pediatric Item Bank - Peer Relationships - Week 12

    A higher score indicates a more positive experience in relationships with peers

    Time frame: Week 12

  17. PROMIS Pediatric Item Bank - Peer Relationships - Week 24

    A higher score indicates a more positive experience in relationships with peers

    Time frame: Week 24

  18. NIH Toolbox - General Life Satisfaction - Week 6

    A higher score indicates more life satisfaction

    Time frame: Week 6

  19. NIH Toolbox - General Life Satisfaction - Week 12

    A higher score indicates more life satisfaction

    Time frame: Week 12

  20. NIH Toolbox - General Life Satisfaction - Week 24

    A higher score indicates more life satisfaction

    Time frame: Week 24

  21. PROMIS Pediatric Short Form v1.0 - Positive Affect - Week 6

    A higher score indicates more positive affect

    Time frame: Week 6

  22. PROMIS Pediatric Short Form v1.0 - Positive Affect - Week 12

    A higher score indicates more positive affect

    Time frame: Week 12

  23. PROMIS Pediatric Short Form v1.0 - Positive Affect - Week 24

    A higher score indicates more positive affect

    Time frame: Week 24

  24. Rosenberg Self-Esteem Scale (RSES) - Week 6

    A higher score indicates higher self-esteem

    Time frame: Week 6

  25. Rosenberg Self-Esteem Scale (RSES) - Week 12

    A higher score indicates higher self-esteem

    Time frame: Week 12

  26. Rosenberg Self-Esteem Scale (RSES) - Week 24

    A higher score indicates higher self-esteem

    Time frame: Week 24

07

Study locations

1 of 1 sites recruiting
  • University of Minnesota
    Minneapolis, Minnesota 55455, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07129070
Lead sponsor
University of Minnesota
Responsible party
Sponsor
First posted
Aug 19, 2025
Start date
Dec 18, 2025
Primary completion
Apr 1, 2028 (estimated)
Completion
May 31, 2028 (estimated)
Last update
Apr 24, 2026

Study contacts

Gracie Meyer
Contact
meye3329@umn.edu
612-625-7240
Meredith Gunlicks-Stoessel, PhD, LP
principal investigator · University of Minnesota
Lindsey Weiler, PhD
principal investigator · University of Minnesota

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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