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Combined Transcranial Magnetic Stimulation and Cognitive Treatment in Blast Traumatic Brain Injury

Combining Cognitive Treatment With Noninvasive Brain Stimulation in Blast TBI

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01596569
Acronym
COST-TBI
Enrollment
15
Registered
2012-05-11
Start date
2012-05-31
Completion date
2017-11-18
Last updated
2018-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blast Injury, Cognitive Dysfunction, Traumatic Brain Injury

Keywords

Blast Traumatic Brain Injury, Cognitive Rehabilitation, Transcranial Magnetic Stimulation, Combined Treatment

Brief summary

This study investigates the efficacy of a novel neurorehabilitation program combining noninvasive brain stimulation (transcranial magnetic stimulation or TMS) and cognitive therapy, on cognitive function and quality of life in individuals with blast-induced traumatic brain injury (bTBI).

Detailed description

The most common blast-induced traumatic brain injury (bTBI)-associated problems are cognitive deficits, such as executive functioning and memory. This study evaluates a combined rehabilitation program: transcranial magnetic stimulation (TMS) and cognitive therapy for treatment of patients with bTBI. TMS is a noninvasive way of stimulating the brain, which is not painful and does not involve any needles or any form of surgery. It acts by delivering a magnetic stimulation to a particular brain region. Half of the study participants will receive cognitive intervention with active TMS, and a control group will receive cognitive intervention with sham TMS. This study takes place in Boston, Massachusetts: at the VA Boston Healthcare System and Beth Israel Deaconess Medical Center.

Interventions

DEVICERepetitive Transcranial Magnetic Stimulation (rTMS)

Daily rTMS treatment for one week. Sham TMS participants receive the same study procedures as patients receiving active TMS.

BEHAVIORALCognitive Intervention

Cognitive intervention designed specifically to address the most common cognitive deficits (executive function and memory) in bTBI. All participants receive weekly cognitive treatment sessions for 10 weeks.

Sponsors

Boston Medical Center
Lead SponsorOTHER
National Center for Research Resources (NCRR)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DEVICE_FEASIBILITY
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* OEF/OIF active-duty personnel or veterans exposed to blast * Meets criteria for mild TBI * LOC of 30 min or less * Age: 21-50 * Primary language is English

Exclusion criteria

* Evidence of penetrating head injury * History of previous neurological diagnosis * History of previous psychotic disorder prior to the blast exposure * Hearing or vision impairment

Design outcomes

Primary

MeasureTime frameDescription
Post concussive symptoms in TBI4 weeksNeurobehavioral Symptoms Inventory (NSI) is a 22-item measure that assesses the post-concussive symptoms in patients with TBI.The NSI asks the patient to rate each of the symptoms according to how much the symptom has disturbed him/her using a five point scale. Patient ratings are based on descriptions of the frequency of the symptom, the extent to which the symptom disrupts the patient's activities, and the patient's perceived need for help with the symptom. A total score will be summated. Lower scores are more favorable.

Secondary

MeasureTime frameDescription
Daily life and functional outcome4 weeksDysexecutive Questionnaire (DEX) is a 20-item self-report measure of real-life deficits relevant to cognitive/executive function that measures four domains: emotional, motivational, behavioral and cognitive. All items are rates in terms of frequency on a 5-point scale: 0 (never), 1(occasionally), 2 (sometimes), 3 (fairly often), 4 (very often). Scores are summed and the total scores range from 0 to 80, with higher scores indicating greater problems with executive functioning.
PTSD symptoms4 weeksMilitary version (PCL-M) 17-item self-report measure that assesses PTSD symptoms. Each item is scored on the frequency of the problem from 1 to 5 where 1= not at all and 5= extremely. A total score is calculated and lower scores are more favorable..

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026