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Clinical Trials/NCT05340296
NCT05340296
Terminated
N/A

Network Health Intervention for Adolescents Leaving Acute Psychiatric Care

University of Rochester1 site in 1 country19 target enrollmentJuly 1, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Suicide, Attempted
Sponsor
University of Rochester
Enrollment
19
Locations
1
Primary Endpoint
Number of youth who complete the intervention
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this pilot study is to refine and then assess the feasibility, acceptability, and target engagement of Acute Youth Connect - a network health intervention for adolescents leaving acute psychiatric care with suicide-related concerns.

Detailed Description

This pilot study includes only one arm of subjects, all of whom will receive Acute Youth Connect, in addition to treatment as usual. The Acute Youth Connect treatment protocol lasts for 12 weeks following discharge, for a total intervention period of roughly 13 weeks including pre-discharge consent and nomination of supports. Patients will be assessed at baseline, mid-intervention, immediately post-intervention, and 12 weeks following the scheduled intervention completion. Feedback from the first 5-10 patients will be used to modify the treatment protocol to improve patient acceptability. All remaining patients will receive this refined treatment protocol. At the time of registration, the Acute Youth Connect treatment protocol is as follows. Adolescents in acute psychiatric care (partial hospitalization) will be screened for eligibility approximately one week before discharge. After patient assent and parental consent are received, the patient and a parent/caregiver will together nominate 3-4 trusted adults in the patient's life to serve as a post-discharge support team. The nominees will then be contacted, consented, and receive a 45-90 minute training on how to provide social support to the patient. Each adult support will also receive weekly (3-15 minute) check in calls from study staff to monitor progress and resolve any concerns related to the patient's progress. In addition, each patient will attend 3 interactive sessions with a study interventionist, and will be encouraged to bring an adult from their support team to participate as well. These sessions will be evenly spaced throughout the post-discharge intervention period. Adolescents will receive weekly reflection-prompting text messages to practice skills taught in the interactive sessions.

Registry
clinicaltrials.gov
Start Date
July 1, 2022
End Date
October 6, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ian Cero

Senior Instructor

University of Rochester

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Number of youth who complete the intervention

Time Frame: Interactive sessions by the end of the 12-week intervention.

Youth subjects who complete all three interactive sessions will be marked as "treatment completers."

Text message responses

Time Frame: A text message must be responded to before the next text message prompt is sent (roughly one week).

Text message prompts will be marked as "responded to" when a recipient produces at least one reply.

Adult support team treatment completion

Time Frame: Psychoeducation sessions must be completed before week 4 after youth's discharge. Check-in calls must be completed in seperatecalendar weeks, all before the end of the 12-week intervention.

Adult support team members who complete their initial psychoeducation training session and complete 75% of their check-in phone calls will be marked as "treatment completers".

Secondary Outcomes

  • Change in weekly contact to supportive adults in their lives(Baseline to 3 months post-treatment, approximately 6 months)
  • Utilization of intervention content(Baseline to 3 months post-treatment, approximately 6 months)

Study Sites (1)

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