Non-invasive vagal nerve stimulation and sleep
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StatusAccepting Candidates
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Age18 Years - 55 Years
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SexesAll
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Healthy Volunteers
Description
This study is investigating if using a stimulation devise can improve quality of sleep for veterans suffering from PTSD.
Details
Protocol number | 201700541 |
Eligibility
Inclusion
Between 18 and 50 years old Veteran Meets PTSD criteria (consider a combination of the following):
PTSD dx Meets criteria for all PTSD DSM-5 criteria on CAPS-5 (A-E) and symptoms have lasted for at least one month
Exclusion
TBI < 6 months ago Current significant neurologic (e.g., dementia, stroke) or psychiatric illness (e.g., bipolar disorder, schizophrenia) History of major psychiatric illness prior to PTSD (e.g., bipolar disorder, schizophrenia) Untreated sleep apnea Habitual sleeping conditions that cannot be realistically recreated Prescribed medications that can interfere with the autonomic nervous system Current illicit or prescription drug abuse Current marijuana or alcohol use beyond low risk Currently pregnant
Lead researcher
Participate in a study
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Step1
Contact the research team
Call or email the research team listed within the specific clinical trial or study to let them know that you're interested. A member of the research team, such as the researcher or study coordinator, will be available to tell you more about the study and to answer any questions or concerns you may have.
Primary contact
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Step2
Get screened to confirm eligibility
You may be asked to take part in prescreening to make sure you are eligible for a study. The prescreening process ensures it is safe for you to participate. During the prescreening process, you will be asked some questions and you may also be asked to schedule tests or procedures to confirm your eligibility.
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Step3
Provide your consent to participate
If you are eligible and want to join the clinical trial or study, a member of the research team will ask for your consent to participate. To give consent, you will be asked to read and sign a consent form for the study. This consent form explains the study's purpose, procedures, risks, benefits and provides other important information, such as the study team's contact information.
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Step4
Participate
If you decide to participate in a clinical trial or study, the research team will keep you informed of the study requirements and what you will need to do to throughout the study. For some trials or studies, your health care provider may work with the research team to ensure there are no conflicts with other medications or treatments.