This study is not yet accepting patients

Veteran's Interdisciplinary Care for Traumatic Brain Injury and Co-Occurring Disorders Rehabilitation Trial

a study on Brain Injury Traumatic Brain Injury

Summary

Eligibility
for people ages 18-65 (full criteria)
Dates
study started
study ends around

Description

Summary

The goal of this clinical trial is to learn if the Avalon Action Alliance Interdisciplinary Outpatient Rehabilitation Program (IORP) can reduce long-lasting symptoms of traumatic brain injury (TBI) and co-occurring disorders in veterans and first responders. The main questions it aims to answer are:

  • Does a 3-week IORP reduce symptoms of long-lasting TBI and co-occurring disorders in military veterans and first responders?
  • Does the 3-week IORP improve life quality and function in military veterans and first responders?

Researchers will compare the Control group to the Invention group to see if a 3-week of IORP reduced symptoms of TBI and co-occurring disorders in military veterans and first responders.

Participants will complete the following activities. The items with an asterisk(*) are not required or available at all sites.

Official Title

Veteran's Interdisciplinary Care for Traumatic Brain Injury & Co-Occurring Disorders Rehabilitation Trial - A Pragmatic, Randomized, Controlled Clinical Trial

Keywords

Traumatic Brain Injury and Co-occurring Disorders, Traumatic Brain Injury, Veterans, First Responders, TBI, Interdisciplinary Outpatient Rehabilitation Program, IORP, Traumatic Brain Injuries, 3-week interdisciplinary outpatient rehab program (IORP)

Eligibility

You can join if…

Open to people ages 18-65

  • Meets general eligibility requirements for site specific 3-week IORP
  • Capable of providing informed consent for IORP and study participation
  • English speaking
  • 18 to 65 years old

You CAN'T join if...

  • History of TBI of any severity in the past 6 months
  • Active substance use disorder that precludes study participation
  • Neurologic, psychiatric, or other medical condition that would prohibit full study participation
  • Active-duty military service member
  • Any other circumstance that, in the opinion of the investigator, would undermine the integrity or success of the project

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
Medical College of Wisconsin
ID
NCT07463027
Study Type
Interventional
Participants
Expecting 416 study participants
Last Updated