Can a headband ward off PTSD in firefighters?
NCT ID NCT06203717
First seen Jun 27, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This small study looked at whether firefighters could use a mild brain stimulation device (CES) at home for four weeks. The goal was to see if it's practical and if it helps with symptoms of depression, anxiety, and posttraumatic stress. Thirteen active-duty firefighters participated, using the device daily and reporting their mood and fatigue.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
13 people
The number who actually took part.
- Started
-
Apr 2024
- Finished
-
Jun 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 56 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Active duty firefighter in Rhode Island, USA; * Age between 18 and 56 years old; * Be in good medical health or, if having chronic medical conditions, these conditions needed to be stable; * Ability to speak, read, write, and understand English sufficiently well to complete study procedures and provide informed consent. Exclusion Criteria: * MRI and CES-related contraindications, e.g., implanted metallic device or substances including pacemakers, cochlear implant, metallic tattoos, claustrophobia, pregnancy or planning to become pregnant during the study duration and nursing; * Neurological conditions such as brain neoplasm, cerebrovascular events, epilepsy or history of seizures, dementia, and neurodegenerative disorders, or had previously received brain surgery; * Report presence of suicidal ideation on QuickSCID-5 or has attempted suicide one or more times within the past twelve months; * Exhibiting a psychiatric condition that would require inpatient or partial psychiatric hospitalization; * Current moderate or severe alcohol or other substance abuse (excluding nicotine); * Major or unstable medical illness requiring further investigation or treatment.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Adults are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Butler Hospital
Providence, Rhode Island, 02906, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a broader rehab programme help people with low vision live better?
- Can online workouts bring fitness to adults with cerebral palsy?
- A simple blood test could curb antibiotic overuse in indonesia
- Could a daily probiotic help you feel fuller and eat less?
- Breathing trick and pill may rewire aging muscles
- Can simple exercises boost strength and balance in older adults?