RECRUITING

UCF Deciding Brains

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 research study is to understand how people make trust-related decisions in healthy aging. Participants will be asked to complete one study session on the University of Central Florida (UCF) campus. The study session will be conducted in a private testing room and include a series of computerized cognitive tasks and learning games, as well as surveys of your beliefs, preferences, and past experiences. The study will take a total of approximately 3.5 hours to completed. You will be allowed to take breaks during the session as needed. If you begin the study but do not complete the session, you will receive credit commensurate with your participation.

Official Title

UCF Deciding Brains

Quick Facts

Study Start:2023-09-21
Study Completion:2029-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06176092

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:20 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Younger adults only: Age 20-39 years old
  2. * Older adults only: Age 60 years old and older
  3. * Fluent English speaker
  4. * At least 8th grade education
  5. * On a stable regimen of medications
  6. * Able to provide verbal and written informed consent
  7. * Normal cognitive function
  8. * Older adults only: The above will be assessed/confirmed via cognitive screening assessments
  9. * Telephone Interview for Cognitive Status (TICS-M; see "Telephone Interview for Cognitive Status" in Local Site Documents)
  1. * Pregnant
  2. * Presence of:
  3. * Schizophrenia Spectrum or Other Psychotic Disorders
  4. * Bipolar and Related Disorders
  5. * Depressive Disorders
  6. * Anxiety Disorders
  7. * Trauma- and Stressor-Related Disorders
  8. * Substance-Related and Addictive Disorders
  9. * Current anticonvulsant, neuroleptic, or sedative use
  10. * Uncorrected visual and hearing impairments
  11. * Neurologic condition or event affecting the brain in the last 12 months (e.g., stroke, epilepsy, traumatic brain injury with \>30-minute loss of consciousness)
  12. * History of brain surgery including tumor resection, deep brain resection, pallidotomy, and thalamotomy
  13. * Unstable medical illness (e.g., metastatic cancer)
  14. * Significant cardiovascular condition or event in the last 12 months (e.g., major heart attack, heart bypass surgery

Contacts and Locations

Study Contact

Amoy Fraser, PhD
CONTACT
4072668742
amoy.fraser@ucf.edu
Erica Martin, B.S.
CONTACT
4072668742
erica.martin@ucf.edu

Principal Investigator

Nichole Lighthall, PhD
PRINCIPAL_INVESTIGATOR
University of Central Florida

Study Locations (Sites)

University of Central Florida
Orlando, Florida, 32827
United States

Collaborators and Investigators

Sponsor: University of Central Florida

  • Nichole Lighthall, PhD, PRINCIPAL_INVESTIGATOR, University of Central Florida

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 Date2023-09-21
Study Completion Date2029-01

Study Record Updates

Study Start Date2023-09-21
Study Completion Date2029-01

Terms related to this study

Keywords Provided by Researchers

  • Healthy
  • Psychology

Additional Relevant MeSH Terms

  • Trust