ACTIVE_NOT_RECRUITING

Tele-Rehabilitation to Improve Mild Traumatic Brain Injury Recovery and Reduce Subsequent Injury Risk

Conditions

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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 goal of this clinical trial is to examine the feasibility, utility, and efficacy of a smartphone-based assessment battery and remotely administered virtual Neuromuscular/Dual-Task (vNDT) intervention among healthy U.S. military service members and physically active young adults with a recent concussion.

Official Title

Tele-Rehabilitation to Improve Mild Traumatic Brain Injury Recovery and Reduce Subsequent Injury Risk

Quick Facts

Study Start:2023-08-23

Study Completion:2025-09-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05594225

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 Criteria	Exclusion Criteria
* 18-40 years of age at the time of enrollment * Mild TBI or concussion diagnosis by a physician * Confirmed MTBI diagnosis via VA/DOD guidelines at time of enrollment * Participation in regular physical activity prior to injury (confirmed via the Global Physical Activity Questionnaire \[GPAQ\]) (Cleland et al., 2014; Keating et al., 2019) * Access to a smartphone for app download	* Moderate or severe TBI * Pre-injury neurological disorder * Abnormal brain imaging findings (if performed as a part of routine care) * Previous TBI (mild/moderate/severe) \<12 months prior to enrollment other than the current injury for which they are being seen

Contacts and Locations

Principal Investigator

David R Howell, PhD

PRINCIPAL_INVESTIGATOR

University of Colorado School of Medicine

Study Locations (Sites)

University of Colorado Denver

Aurora, Colorado, 80045

United States

Brooke Army Medical Center

Fort Sam Houston, Texas, 78236

United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

David R Howell, PhD, PRINCIPAL_INVESTIGATOR, University of Colorado School of Medicine

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 Date2023-08-23

Study Completion Date2025-09-30

Study Record Updates

Study Start Date2023-08-23

Study Completion Date2025-09-30

Terms related to this study

Additional Relevant MeSH Terms

Brain Concussion