Actively Recruiting
Recovery Among Older Adults Following Mild TBI
Led by University of Maryland, Baltimore · Updated on 2026-05-06
250
Participants Needed
1
Research Sites
294 weeks
Total Duration
On this page
Sponsors
U
University of Maryland, Baltimore
Lead Sponsor
N
National Institute on Aging (NIA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Among fall related injuries in older adults, head injuries are the most common, yet almost nothing is known about recovery from head injury, also known as traumatic brain injury or TBI, in this population. The RETRO-TBI study is a prospective cohort study of 250 adults aged 65 and older with mild TBI to evaluate recovery in cognitive, physical and psychological function and sleep quality at four timepoints (2 weeks and 3, 6, and 12 months) over the year following injury and identify factors associated with recovery trajectories. The potential impact of this work is that it will generate new knowledge that will guide targeted treatment efforts and inform future development of strategies to optimize recovery following this common fall-related injury among older adults.
CONDITIONS
Official Title
Recovery Among Older Adults Following Mild TBI
Who Can Participate
Eligibility Criteria
You may qualify if you...
Inclusion Criteria
-
Aged 65 years or older
-
Treated for mild TBI (defined below) at the R Adams Cowley Shock Trauma Center (STC) or at one of six University of Maryland Affiliated Hospitals within 72 hours of injury
-
Mild TBI was defined as:
- Traumatically induced physiological disruption of brain function, as manifested by at least one of the following 1) loss of consciousness ≤30 minutes, post-traumatic amnesia <24 hours, observed or self-reported transient confusion, disorientation, or impaired consciousness, or neurologic deficit as defined by a Glasgow Coma Scale (GCS) score of 13-14 on admission.
- GCS of 15 with no other evidence of mild TBI was also accepted with positive computed tomography image.
Exclusion criteria
- Injury to any other body region resulting in an abbreviated injury scale (AIS) score >2
- Anticipation that patient would not be ambulatory at 2-weeks post-injury
- History of dementia as determined by patient/proxy report or medical history
- Non-ambulatory pre-injury
- No available proxy
- Not English speaking
- Prisoners
- Live >55 miles from the STC.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Maryland, Baltimore
Baltimore, Maryland, United States, 21201
Actively Recruiting
Research Team
J
Jennifer Albrecht, PhD
CONTACT
M
Michelle Newman, BSN
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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