RECRUITING

Swift Outpatient Alternatives for Rapid Stabilization

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to improve the effective outpatient management of acute youth suicide risk by optimizing intervention components to build an efficient, evidence-based intervention that is responsive to the needs of, and coordinated with, providers in primary care settings. The main questions are: 1. What is the strongest combination of SOARS components associated with reduction in youth suicidal thoughts and behavior (STB)? 2. Do age and STB history moderate the impact of the effects of the SOARS intervention components? 3. Do therapeutic alliance, youth and caregiver self-efficacy account for changes in youth STBs? 4. What helps medical outpatient providers refer to SOARS and continue care after SOARS?

Official Title

Swift Outpatient Alternatives for Rapid Stabilization

Quick Facts

Study Start:2023-11-09
Study Completion:2028-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05996172

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:13 Years to 21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Acute suicidal thoughts or past month suicide attempt as reported on positive responses to the Ask Suicide Screening Questionnaire (ASQ),
  1. * urgent medical care secondary to self-injurious behavior, psychosis, eating disorder that requires full or partial inpatient care, or
  2. * intellectual disability warranting a different treatment pathway;
  3. * limited English, Spanish, Vietnamese, or Chinese proficiency that would interfere with ability to complete study assessments;
  4. * unwillingness to participate in psychotherapy,
  5. * caregiver unwilling or ineligible to participate;
  6. * and previous enrollment in SOARS program or other P50 project as to not confuse longitudinal follow-up.

Contacts and Locations

Study Contact

Molly Adrian
CONTACT
206-987-7183
molly.adrian@seattlechildrens.org

Principal Investigator

Molly Adrian, Ph.D.
PRINCIPAL_INVESTIGATOR
University of Washington

Study Locations (Sites)

Seattle Children's
Seattle, Washington, 98199
United States

Collaborators and Investigators

Sponsor: University of Washington

  • Molly Adrian, Ph.D., PRINCIPAL_INVESTIGATOR, University of Washington

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-11-09
Study Completion Date2028-01

Study Record Updates

Study Start Date2023-11-09
Study Completion Date2028-01

Terms related to this study

Additional Relevant MeSH Terms

  • Suicidal Ideation
  • Suicide Attempt