COMPLETED

Individualized Vocational and Educational Support and Training for Clinical High Risk for Psychosis (InVEST)

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 test the efficacy of InVEST (Individualized Vocational and Educational Support and Training) for CHR-P (clinical high risk for psychosis) to address specific role functioning difficulties associated with the CHR-P phase. Our specific goals are: 1. Part 1: Preliminary open trial of InVEST (n = 8) to collect preliminary feasibility and acceptability data by providing the intervention, administering assessments, and collecting focus group and self-report feedback from open trial participants. The open trial phase will help to refine recruitment approaches and to modify the treatment manual as needed. 2. Part 2: Preliminary randomized controlled trial of InVEST vs. Delayed InVEST (DI) to explore preliminary evidence of efficacy of InVEST vs. DI (n = 30). The investigators hope to gain understanding of the feasibility of InVEST and the study's assessment procedures, and to gain a preliminary understanding of the intervention's efficacy for functioning difficulties experienced by young people at CHR-P.

Official Title

Individualized Vocational and Educational Support and Training for Clinical High Risk for Psychosis (InVEST)

Quick Facts

Study Start:2022-02-22
Study Completion:2025-09-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05114733

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:12 Years to 22 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Principal Investigator

Michelle Friedman-Yakoobian, PHD
PRINCIPAL_INVESTIGATOR
Department of Psychiatry at BIDMC - a major teaching hospital of Harvard Medical School

Study Locations (Sites)

Beth Israel Deaconess Medical Center/ Massachusetts Mental Health Center
Boston, Massachusetts, 02115
United States

Collaborators and Investigators

Sponsor: Beth Israel Deaconess Medical Center

  • Michelle Friedman-Yakoobian, PHD, PRINCIPAL_INVESTIGATOR, Department of Psychiatry at BIDMC - a major teaching hospital of Harvard Medical School

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 Date2022-02-22
Study Completion Date2025-09-15

Study Record Updates

Study Start Date2022-02-22
Study Completion Date2025-09-15

Terms related to this study

Keywords Provided by Researchers

  • clinical high risk for psychosis
  • psychosis risk syndrome
  • school functioning
  • intervention

Additional Relevant MeSH Terms

  • Clinical High Risk for Psychosis