RECRUITING

Verbal Working Memory and Attention Remediation for Adults With Traumatic Brain Injury.

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 will examine if computerized cognitive remediation will improve working memory and attention in 25 adults with a mild, moderate, or severe brain injury and compare their cognitive performance to the control group of 25 adults with a mild, moderate, or severe brain injury. The control group will train on computerized tasks of social awareness. Participants in both groups will be assessed prior to training and immediately post-training and one month-post training.

Official Title

Verbal Working Memory and Attention Remediation for Adults With Traumatic Brain Injury.

Quick Facts

Study Start:2021-08-01
Study Completion:2026-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04349852

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Medically documented mild, moderate, or severe TBI;
  2. * All subjects will be older than 18 years of age;
  3. * Free from schizophrenia or bipolar disorder, due to the potential influence of such disorders on cognitive functioning;
  4. * Free of current alcohol or drug abuse;
  5. * At least 3 months post-injury.
  1. * Younger than 18 years old.
  2. * A brain injury that is not medically documented.
  3. * Being diagnosed with schizophrenia or bipolar disorder.
  4. * Current alcohol or drug use diagnosis
  5. * Less than 3 months post-injury

Contacts and Locations

Study Contact

Gerald Voelbel, PhD
CONTACT
212-998-5827
gv23@nyu.edu

Principal Investigator

Gerald Voelbel, PhD
PRINCIPAL_INVESTIGATOR
NYU Langone Health

Study Locations (Sites)

NYU Langone Health
New York, New York, 10016
United States

Collaborators and Investigators

Sponsor: NYU Langone Health

  • Gerald Voelbel, PhD, PRINCIPAL_INVESTIGATOR, NYU Langone Health

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 Date2021-08-01
Study Completion Date2026-12-01

Study Record Updates

Study Start Date2021-08-01
Study Completion Date2026-12-01

Terms related to this study

Additional Relevant MeSH Terms

  • Traumatic Brain Injury