Cereset Research Exploratory Study
A legfontosabb adatok
- Hol
- Winston-Salem (Egyesült Államok)A helyszín megnézése
Helyszínek itt: Egyesült Államok
- Wake Forest University Health Scienc\essWinston-Salem, Egyesült ÁllamokContact: Kenzie BrownRésztvevőt keres
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Wake Forest University Health Sciences
- Azonosító
- NCT03777267
- A regiszteradat frissítve
- 2026. július 20.
- Eredeti leírás
The purpose of this study is to evaluate the use of Cereset Research to improve autonomic function in participants with symptoms of stress, anxiety, or insomnia.A teljes eredeti leírásKevesebb
The purpose of this study is to evaluate the use of Cereset Research to improve autonomic function in participants with symptoms of stress, anxiety, or insomnia.
Bevonási feltételek: Subjects must have the ability to comply with basic instructions and be able to sit still comfortably with the sensor leads attached; Subjects experiencing symptoms of stress, anxiety, or insomnia, who meet threshold scores on one or more self-reported inventories for the same. This includes the Insomnia Severity Index (ISI, ≥ 8), the Perceived Stress Index (PSS, ≥ 14), or the Generalized Anxiety Disorder 7-item (GAD-7, ≥ 5) scale.
Kizáró feltételek: Prior use of HIRREM, Brainwave Optimization, Cereset, or a wearable configuration of the same (B2, or B2v2) within the last 3 years; Prior use of electroconvulsive therapy (ECT); Prior use of transcranial magnetic stimulation (TMS), transcranial direct current stimulation (TDCS), alpha stimulation, neurofeedback, biofeedback, or deep brain stimulation (DBS) within one month before enrollment; Severe hearing impairment (because the subject will be using ear buds during CR); Known seizure disorder; Unable, unwilling, or incompetent to provide informed consent/assent; Physically unable to come to the study visits, or to sit comfortably in a chair for up to 1.5 hours; Weight is over the chair limit (285 pounds); Currently in another active intervention research study.