RECRUITING

S.T.A.N.D. Alacrity Center Signature Project

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 purpose of this study is to evaluate clinical decision-making algorithms for (a) triaging to level of care and (b) adapting level of care in a low income, highly diverse sample of community college students at East Los Angeles College (ELAC). The target enrollment is 200 participants per year, for five years (N=1000). Participants are between the ages of 18 and 40 years and will be randomized into either symptom severity decision-making (SSD) or data-driven decision-making (DDD). Participants in each condition will be triaged to one of three levels of care, including self-guided online prevention, coach-guided online cognitive behavioral therapy, and clinician-delivered care. After initial triaging, level of care will be adapted throughout the entire time of the study enrollment. Participants will complete computerized assessments and self-report questionnaires as part of the study. The total length of participation is 40 weeks.

Official Title

Screening and Treatment for Anxiety & Depression (S.T.A.N.D): Alacrity Center Signature Project on Triaging and Adapting to Level of Care

Quick Facts

Study Start:2022-08-29
Study Completion:2027-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05591937

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:18 Years to 40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Currently enrolled in the East Los Angeles College
  2. * Either uninsured or covered by California Medicaid
  3. * Own or have private access to internet to complete the assessments and online prevention and therapy programs
  1. * Unable to fully comprehend the consent form, respond adequately to screening questions, or maintain focus or to sit still during assessment
  2. * Diagnosed with disorders requiring more specialized care (e.g., psychotic disorder, severe eating disorder, severe substance use disorder, severe neurological disorder), or marked cognitive impairment
  3. * Currently treated by psychiatrist or psychologist during timeframe that the treatment is offered through STAND and is unwilling to fully transfer care to STAND

Contacts and Locations

Study Contact

Amelia Welborn, Ph.D.
CONTACT
916-202-5952
awelborn@mednet.ucla.edu
Alainna Wen, Ph.D.
CONTACT
AAWen@mednet.ucla.edu

Principal Investigator

Michelle Craske, Ph.D
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles
Kate Taylor, Ph.D
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles

Study Locations (Sites)

East Los Angeles College
Los Angeles, California, 91754
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

  • Michelle Craske, Ph.D, PRINCIPAL_INVESTIGATOR, University of California, Los Angeles
  • Kate Taylor, Ph.D, PRINCIPAL_INVESTIGATOR, University of California, Los Angeles

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 Date2022-08-29
Study Completion Date2027-04-30

Study Record Updates

Study Start Date2022-08-29
Study Completion Date2027-04-30

Terms related to this study

Keywords Provided by Researchers

  • personalized care
  • cognitive behavioral therapy
  • depression
  • anxiety

Additional Relevant MeSH Terms

  • Depression
  • Anxiety