CBITS-RTM Pilot Study
2. juli 2026 opdateret af: University of California, San Francisco
Preventing Substance Use Among Incarcerated Youth Through Addressing Posttraumatic Stress
This pilot study, conducted in partnership with juvenile detention centers, evaluates an adapted CBITS-RTM intervention delivered in a detention school setting.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Detaljeret beskrivelse
The study examines the intervention's feasibility and acceptability, as well as its effectiveness in reducing incarcerated youth's posttraumatic stress symptoms, improving academic functioning, and decreasing intentions to use substances post-release.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
28
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Johanna B Folk, PhD
- Telefonnummer: 415-602-9521
- E-mail: johanna.folk@ucsf.edu
Undersøgelse Kontakt Backup
- Navn: Jeanne McPhee, PhD
- E-mail: jeanne.mcphee@ucsf.edu
Studiesteder
-
-
California
-
San Francisco, California, Forenede Stater, 94131
- UCSF Zuckerberg San Francisco General Hospital
-
Kontakt:
- Principal Investigator, PhD
- E-mail: johanna.folk@ucsf.edu
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:
- Youth must 1) be currently incarcerated in a partnering juvenile detention center, 2) be between 13-18 years of age, and 3) have a minimum of 3 months remaining on their sentence (i.e., sufficient time required to complete CBITS-RTM). Youth will complete a screening with a study team member involving the 2-item Abbreviated PTSD Checklist-Civilian version, with scores ≥4 considered a positive screen
- Clinicians are eligible if they are behavioral health staff working with youth at the detention school..
Exclusion Criteria:
- Observable cognitive or developmental delays or active psychosis that would interfere with completing consent, assessment or intervention.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Adapted CBITS-RTM Intervention
|
The Cognitive Behavioral Intervention for Trauma in Schools (CBITS) program is a school-based, group and individual intervention designed to reduce symptoms of post-traumatic stress disorder (PTSD), depression, and behavioral problems, and to improve functioning, grades and attendance, and coping skills.
The CBITS intervention was adapted to juvenile justice settings with an added Racial Trauma Module (RTM), which provides youth with an overview of the effects of racism on levels of traumatic stress.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Child PTSD Symptom Scale (CPSS)
Tidsramme: Baseline, 3 months post-baseline
|
The CPSS is used to measure posttraumatic stress among youth (8-18 years).
It assesses past month posttraumatic stress symptom severity and impairment of endorsed symptoms on daily functioning.
Scores range from 0-80, with 31+ indicating probable PTSD.
|
Baseline, 3 months post-baseline
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Youth Alcohol and Drug Use Survey
Tidsramme: Baseline, 3 months post-baseline
|
The Youth Alcohol and Drug Use Survey will be used to gather youth's intention to use substances post-release using items rated on a scale from 1 (unlikely) to 10 (very likely).
|
Baseline, 3 months post-baseline
|
|
Texas Christian University (TCU) Drug Screen
Tidsramme: Baseline, 3-months post-baseline
|
The TCU will be administered to gather information on substance use quantity and frequency as well as risk for SUD (corresponds with DSM-5 criteria) on the 3-months prior to incarceration and past 3 months at post-release.
|
Baseline, 3-months post-baseline
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Youth Background Characteristics
Tidsramme: Baseline
|
Demographics questionnaire used to gather standard demographics (e.g., age, gender, race) and information such as state agency involvement (e.g., age at first contact with juvenile legal system, number of prior arrests), immigration status.
|
Baseline
|
|
Treatment Acceptability Form
Tidsramme: 3-months post-baseline
|
This form will be used to assess the acceptability of the adapted CBITS-RTM intervention.
Items are scored from 1 "Strongly disagree" to 5 "Strongly agree."
Scores range from 10-50 with higher scores indicating higher acceptability.
|
3-months post-baseline
|
|
CBITS-RTM Group Evaluation Posttest
Tidsramme: 3-months post-baseline
|
This will assess knowledge of trauma, changes in ability to cope with stress, and acceptability of the intervention and its delivery.
Items are true/false or qualitative in nature.
|
3-months post-baseline
|
|
Clinician personal and professional background characteristics
Tidsramme: Baseline
|
Questionnaire used to gather personal and professional background characteristics (e.g., clinical discipline, experience with trauma treatment, years of practice in juvenile detention setting).
|
Baseline
|
|
Cognitive Behavioral Intervention for Trauma in Schools-Fidelity Adherence Measure 2.0
Tidsramme: 20% of the sessions
|
This measure will be used to assess how closely clinicians adhere to the adapted CBITS-RTM intervention.
The scale describes the core components expected to be covered in each session, and the rater indicates the degree to which each component was delivered with fidelity using a 4-point item rating ranging from 0 (not covered at all) to 3 (covered thoroughly).
Higher item scores indicate greater fidelity to the intervention curriculum.
|
20% of the sessions
|
|
The Evidence-Based Practice Attitude Scale (EBPAS)
Tidsramme: Baseline
|
The EBPAS (15-items) will be used to assess clinician's attitudes toward adopting new evidence-based practices (EBPs).
It consists of four subscales: appeal, requirements, openness, and divergence.
Items are rated on a 5-point Likert scale from 0 (not at all) to 4 (to a very great extent).
Higher scores on the Appeal, Requirements, and Openness subscales indicate more positive attitudes toward adopting EBPs, whereas higher Divergence scores indicate less favorable attitudes.
|
Baseline
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Johanna Folk, PhD, University of California, San Francisco
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. september 2026
Primær færdiggørelse (Anslået)
30. juni 2027
Studieafslutning (Anslået)
31. december 2027
Datoer for studieregistrering
Først indsendt
26. juni 2026
Først indsendt, der opfyldte QC-kriterier
26. juni 2026
Først opslået (Faktiske)
2. juli 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
6. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
2. juli 2026
Sidst verificeret
1. juli 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 25-45799
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .