RECRUITING

Validating an Autonomous Interactive Internet-Based Delivery of an Empirically Supported Cognitive Behavioral Therapy for Comorbidity

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

This project is designed to determine if a computer-delivered cognitive-behavioral treatment can improve the otherwise poor alcohol use disorder treatment outcomes for individuals with a co-occurring anxiety disorder. In the past, the investigators showed that this treatment does improve outcomes for these individuals when delivered by a therapist. If the present work shows that the computer-delivered version is also effective, it would provide an inexpensive program with virtually unlimited scalability to enable access to the treatment by many more individuals than is currently the case.

Official Title

Validating an Autonomous Interactive Internet-Based Delivery of an Empirically Supported Cognitive Behavioral Therapy for Comorbidity

Quick Facts

Study Start:2022-01-04
Study Completion:2026-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05117255

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 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * current (past 30 days) Diagnostic and Statistical Manual of Mental Disorders-IV (DSM-IV) diagnosis of panic disorder with or without agoraphobia (PD/Ag), generalized anxiety disorder (GAD) or social anxiety disorder (SAD)
  2. * receiving treatment primarily for alcohol (vs. drug) dependence
  3. * ability to provide informed consent
  4. * a minimum of an eighth grade English reading level
  5. * status as a residential patient in the Lodging Plus (LP) addiction treatment program
  6. * sufficient time left in their residential LP care to complete the study protocol through the post-treatment assessment
  1. * cognitive or medical impairments that prohibit study participation as determined by study PI
  2. * serious suicide risk determined by study PI
  3. * court-ordered treatment. (The exclusion is based on its classification as a "vulnerable" population.)
  4. * Self-reported past participation in a Kushner intervention study while in Lodging Plus

Contacts and Locations

Study Contact

Nikki Degeneffe
CONTACT
612-625-7546
anxietystudy@umn.edu

Study Locations (Sites)

Lodging Plus Program, Fairview Hospital
Minneapolis, Minnesota, 55454
United States

Collaborators and Investigators

Sponsor: University of Minnesota

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 Date2022-01-04
Study Completion Date2026-03-01

Study Record Updates

Study Start Date2022-01-04
Study Completion Date2026-03-01

Terms related to this study

Additional Relevant MeSH Terms

  • Generalized Anxiety Disorder
  • Panic Disorder
  • Social Anxiety Disorder
  • Alcohol Use Disorder
  • Depression