Screening and Support for Youth (SASY)
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age12-17
SponsorCambridge Health Alliance
About this trial
To adapt the Screening and Support for Youth (SASY) intervention and approach to recruitment for racial, ethnic and linguistic diverse youth aged 12-17 in the Denver Health catchment area
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
12 to 17 year old teens
Disqualifiers
younger than 12 or older than 17
Trial design
Design model
Parallel
Treatments tested in this trial
Behavioral: Screening and Support for Youth (SASY) Multi-component Platform: includes screening, feedback, single session intervention, and resource information
BehavioralDescription: Description: Participants who interact with a QR code and express interest in participating will be randomized to receive either: 1) recruitment from a Research Coordinator (standard research staff approach) or 2) recruitment from an EYE for Prevention Youth Researcher. The process of consent, screening, providing feedback, and offering access to a Single Session Intervention and information on additional resources (per scoring on the screening into Tier 1 (low risk/normal), 2 (moderate/at risk), or 3 (high/clinical risk): Tier 1 = screening+feedback; Tier 2=screening+feedback+SSI; Tier 3=screening+feedback+SSI+resource information) will be the same in each group. The randomization is simply changing who provides the process and platform to the participant.
Behavioral: Screening and Support for Youth (SASY) Multi-component Platform: includes screening, feedback, single session intervention, and resource information
BehavioralDescription: Description: Participants who interact with a QR code and express interest in participating will be randomized to receive either: 1) recruitment from a Research Coordinator (standard research staff approach) or 2) recruitment from an EYE for Prevention Youth Researcher. The process of consent, screening, providing feedback, and offering access to a Single Session Intervention and information on additional resources (per scoring on the screening into Tier 1 (low risk/normal), 2 (moderate/at risk), or 3 (high/clinical risk): Tier 1 = screening+feedback; Tier 2=screening+feedback+SSI; Tier 3=screening+feedback+SSI+resource information) will be the same in each group. The randomization is simply changing who provides the process and platform to the participant.
Treatment groups
220 Participants
are divided into 2 treatment groupsGroup A: Recruitment by Research Coordinator (RC)Other 1 intervention
Group B: Recruitment by EYEOther 1 intervention
Trial outcomes
Primary outcomes
1
Completion of Single session intervention
Number and proportion of participants in Tiers 2 and 3 that start and/or complete the single session intervention. This will be a measure of engagement in services.
Time frame
1 month following initial screening2
Participation
Total number and proportion of 12-17 year olds recruited by the Research Coordinator vs. EYE Youth Researchers; also will examine this by proportion racial, ethnic and linguistic (REL) minoritized youth who participate (comparing Research Coordinator vs. EYE)
Time frame
Immediate at time of enrollmentSecondary outcomes
1
K-CAT/WFIRS scores - preliminary effectiveness
Change on the K-CAT/WFIRS scores between time of screening (pre-) and post-intervention (SSI as the intervention) for Tiers 2 and 3
Time frame
1 month following initial screening2
Therapeutic Alliance
Measure of therapeutic alliance with a) recruitment, screening, feedback and b) SSI.
Time frame
1 month following initial screening3
Engagement in Mental Health Treatment/Behavioral Change Activities
Self-reported measure of engagement for youth who scored in Tier 3 (and were provided SSI + resources).
Time frame
1 month following initial screeningLocations
Sponsors and contacts
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Source ClinicalTrials.gov
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