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Trauma-Informed Peer Aggression and Dating Violence Prevention for Preteens Receiving Intensive Mental Health Services (SPARE)

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Lifespan

Status

Enrolling

Conditions

Teen Dating Violence
Aggression Childhood

Treatments

Behavioral: Treatment as Usual (TAU)
Behavioral: Experimental: Intervention (SPARE) plus Treatment as Usual

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT06769282
K01CE003687 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this clinical trial is to learn if this intervention (Social Skills, Problem Solving, emotion Regulation, and psycho-Education on Trauma: A Trauma-Informed Peer Aggression and Teen Dating Violence Prevention Program; SPARE) can treat peer aggression and prevent teen dating violence in preteens receiving intensive mental health services. The main questions it aims to answer are:

  • Does receiving SPARE reduce proactive and reactive aggression at post-intervention and 3- and 9-month follow-ups?
  • Does receiving SPARE reduce positive attitude about TDV, prevent TDV behaviors, and improve mental health outcomes at post-intervention and 3- and 9-month follow-ups?

Researchers will compare youth receiving SPARE to youth receiving treatment as usual to see if SPARE results in improved proactive and reactive aggression, TDV attitudes and behaviors, and mental health outcomes.

Participants will:

  • Receive SPARE via group therapy incorporated into their daily programing at an intensive mental health program
  • Complete study questionnaires at program intake and discharge as well as at 3-month and 9-month follow-up assessments

Full description

SPARE will include 5 components: (1) Social skills training, including selecting healthy friends and partners, (2) Problem solving with emphasis on positive outcomes of nonaggressive solutions, (3) Awareness of domineering behavior and conflict resolution skills, (4) emotion Regulation, and (5) psycho-Education on ACEs and trauma. SPARE is group-based each of the 5 treatment components are designed to be delivered in two 45-minute sessions per week (see Table 3), for a total of 10 sessions. Each session will include 30 minutes of didactic instruction on the component with developmentally engaging activities to illustrate concepts and an individually tailored 15-minute narrative and mindfulness activity, which may address a traumatic memory depending on youth need and receptivity. SPARE will be delivered by the PI and will replace a social skills group twice a week at CP when it is implemented.

SPARE will be implemented in two sites of a child partial hospitalization program (A & B). Both sites CP serve youth 7-13 years old who (1) require services more intensive than outpatient care or (2) are transitioning from higher care (e.g., inpatient). Youth attend CP for 6 hours a day Monday through Friday. The modal length of stay for youth is 7 weeks. To minimize disruptions in CP care, SPARE will be implemented continuously at one site for 6 months (Active Phase) while TAU data is collected from the other site. After 6 months, conditions at each site will flip, resulting in approximately 5 cohorts of SPARE per site (n=88). Sites A and B will be randomly assigned using yoked randomization to Active Phase or TAU first. During Active Phase, all youth ≥11 years will receive SPARE two days per week (regardless of research eligibility).

Enrollment

88 estimated patients

Sex

All

Ages

11 to 13 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • (1) aged 11-13 years
  • (2) enrolled in CP,
  • (3) ability to write and speak in English
  • (4) parent/guardian consent.

Exclusion criteria

  • None

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

88 participants in 2 patient groups

Intervention (SPARE) plus Treatment as Usual
Experimental group
Description:
Participants assigned to this arm will receive SPARE in the form of group therapy in addition to treatment as usual at a child partial program.
Treatment:
Behavioral: Experimental: Intervention (SPARE) plus Treatment as Usual
Treatment As Usual
Active Comparator group
Description:
Arm Description: Participants assigned to this arm will receive treatment as usual at a child partial program.
Treatment:
Behavioral: Treatment as Usual (TAU)

Trial contacts and locations

1

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Central trial contact

Elizabeth C Tampke, Ph.D.

Data sourced from clinicaltrials.gov

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