RECRUITING

Treatment Optimization of Brain-injured Warfighters

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

Prescribed sub-symptomatic adaptable exercise treatment (SAET) is a potential solution that promotes recovery needs following a TBI. SAET has been shown to benefit the mind and body in ways that decrease the severity and frequency of mild TBI (mTBI) symptoms. This study aims to validate SAET as an alternative, adaptable treatment or SMs with mTBI that focuses on reducing symptoms, improving mental health, increasing physiological functioning, and ultimately returning to duty. The objective of this study is to develop a prescribed exercise treatment program for warfighters with mTBI that can be personalized for SM's needs (i.e., medical and occupational) and is adaptable to various clinical resources (e.g., forward operating bases, rural clinics, and mTBI specialty programs). The key question raised by this study is whether SAET is more effective than a stretching control group (SCG) in reducing neurobehavioral symptoms among SMs with persistent complaints following a mTBI.

Official Title

Treatment Optimization of Brain-injured Warfighters: A Prescribed Sub-symptomatic Exercise Treatment

Quick Facts

Study Start:2023-09-27
Study Completion:2026-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06561100

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 55 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Active duty, male or female, ages 18 to 55
  2. * History of at least one mTBI sustained more than 1 month ago
  3. * Service members (SMs) with ongoing symptoms
  1. * SMs who sustained a TBI of any severity within 1 month of enrollment
  2. * History of moderate, severe, or penetrating TBI
  3. * Current substance use disorder
  4. * History of a neurological disease (e.g., multiple sclerosis, cerebral vascular accident, brain tumor, neurodegenerative disease, or neuro-motor disorder)
  5. * An acute orthopedic injury that limits the capacity to complete study procedures

Contacts and Locations

Study Contact

Jason M Bailie, PhD
CONTACT
(760) 719-4202
jason.m.bailie.ctr@health.mil
Juan J Lopez, BA
CONTACT
(760) 719-4229
juan.j.lopez120.ctr@health.mil

Principal Investigator

Jason M Bailie, Phd
PRINCIPAL_INVESTIGATOR
Traumatic Brain Injury Center of Excellence (TBICoE)

Study Locations (Sites)

Intrepid Spirit Center
Camp Pendleton, California, 92055
United States

Collaborators and Investigators

Sponsor: United States Naval Medical Center, San Diego

  • Jason M Bailie, Phd, PRINCIPAL_INVESTIGATOR, Traumatic Brain Injury Center of Excellence (TBICoE)

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 Date2023-09-27
Study Completion Date2026-09

Study Record Updates

Study Start Date2023-09-27
Study Completion Date2026-09

Terms related to this study

Keywords Provided by Researchers

  • Progressive Return to Activity
  • Warfighter Readiness

Additional Relevant MeSH Terms

  • Mild Traumatic Brain Injury