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Adaptation of the PCIP for Spanish Speaking Adolescents and Families

University of California, Los Angeles (UCLA) logo

University of California, Los Angeles (UCLA)

Status

Withdrawn

Conditions

Post Traumatic Stress Disorder
Post-Traumatic Stress Disorder in Adolescence

Treatments

Behavioral: Waitlist Treatment as Usual
Behavioral: Primary Care Intervention for PTSD Spanish Speaking Adolescents

Study type

Interventional

Funder types

Other

Identifiers

NCT05899322
#22-001744

Details and patient eligibility

About

This study will implement a brief Post-traumatic Stress Disorder (PTSD) intervention for children, the Primary Care Intervention for PTSD (PCIP) delivered through telehealth (computer or smart phone delivery), to 10 Spanish speaking youth and their families.

Mixed methods (qualitative and quantitative) randomized pilot feasibility trial (n=10 to treatment and 10 to waitlist control) to refine the intervention, study procedures, and explore effectiveness.

Following RE-AIM guidelines, the investigators will assess:

Reach: patient participation in intervention delivery (out of all those asked to participate) and retention rate (out of all those who consented to participate and completed at least two intervention sessions) Adoption: patients and their parents/guardians will complete screening and intervention satisfaction ratings.

To understand patient experiences with the intervention and to identify and explain positive or negative treatment mechanisms or effects, the investigators will conduct post-intervention semi-structured interviews with the participating patients, their parents/guardians, and with providers.

This treatment ranges from 1-3 sessions which last 30-50 minutes per session. The first session will cover psychoeducation about PTSD symptoms in children that can be delivered to the parent or both the parent and child. The first session will also teach the parent and child a breathing technique to combat the physiological impact of PTSD in children. The subsequent sessions will be tailored to meet the needs of the child's most distressing PTSD symptom cluster including hyper arousal, negative changes in cognition and mood, avoidance, re-experiencing. Each session contains coping skills that the parent and child can learn together. There is also material for parents to address behavior problems in youth. This treatment will be delivered via telehealth.

All treatment materials have been developed in both Spanish and English.

Sex

All

Ages

12 to 22 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patient referred to the SHARK Program
  • Patients must be at least 12 years old
  • Screened for probable PTSD on Brief UCLA Reaction Index, or at provider discretion of clinical relevancy.
  • If patient is under 18 years old, the patient's legal guardian is able and willing to provide informed consent for the patient to participate in the study in English or Spanish;
  • Patient is able to complete study activities in English or Spanish.

Exclusion criteria

  • Suicidal ideation with a plan within the last two weeks or a suicide attempt within the past 30 days;
  • Patient is over the age of 22

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Primary Care Intervention for PTSD (PCIP) Spanish Speaking Adolescents and Families
Experimental group
Description:
This arm will receive the culturally adapted and translated PCIP intervention lasting from 1-3 weeks, and will complete baseline, post treatment, and 1-month follow up assessments.
Treatment:
Behavioral: Primary Care Intervention for PTSD Spanish Speaking Adolescents
Waitlist Treatment as Usual
Active Comparator group
Description:
Receive standard care treatment and will complete baseline, post treatment, and 1-month follow up assessments, and are offered translated and adapted PCIP treatment after conclusion of the study.
Treatment:
Behavioral: Waitlist Treatment as Usual

Trial contacts and locations

1

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Central trial contact

Gray K Bowers, MA; Lauren C Ng, PhD

Data sourced from clinicaltrials.gov

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