[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cardiovascular-conditions-after-birth\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cardiovascular-conditions-after-birth":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":5},"100345405","cereset-research-exploratory-study-100345405",false,"NCT03777267","Cereset Research Exploratory Study","Inclusion Criteria:\n\n* Subjects must have the ability to comply with basic instructions and be able to sit still comfortably with the sensor leads attached\n* 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.\n\nExclusion Criteria:\n\n* Unable, unwilling, or incompetent to provide informed consent\u002Fassent.\n* Physically unable to come to the study visits, or to sit comfortably in a chair for up to 1.5 hours.\n* Severe hearing impairment (because the subject will be using ear buds during CR).\n* Weight is over the chair limit (285 pounds).\n* Currently in another active intervention research study.\n* Prior use of HIRREM, Brainwave Optimization, Cereset, or a wearable configuration of the same (B2, or B2v2) within the last 3 years.\n* Prior use of electroconvulsive therapy (ECT).\n* 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.\n* Known seizure disorder.","ALL","11 Years",{"count":18,"type":19},200,"ESTIMATED","INTERVENTIONAL",[22],"NA","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.",[25,26,27],"Neurological Diseases or Conditions","Cardiovascular Conditions After Birth","Psychophysiologic Disorders",[29,30,31,32,33,34,35,36,37,38],"Stress","Neurotechnology","Autonomic Dysregulation","Hyperarousal","Brain electrical activity","Allostasis","HIRREM","Cereset Research","Insomnia","Anxiety","RECRUITING","2026-04-28",{"date":42,"type":43},"2026-05-04","ACTUAL",{"date":45,"type":43},"2019-04-12",{"date":47,"type":19},"2028-04",{"name":49,"class":50},"Wake Forest University Health Sciences","OTHER"]