Neurological Diseases or Conditions Clinical Trial
Official title:
Cereset Research Exploratory Study
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.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | January 2026 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 11 Years and older |
Eligibility | Inclusion Criteria: - 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. Exclusion Criteria: - 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. - Severe hearing impairment (because the subject will be using ear buds during CR). - Anticipated and ongoing use of alcohol or recreational drugs. - Weight is over the chair limit (285 pounds). - Currently in another active intervention research study. - Prior use of HIRREM, Brainwave Optimization, Cereset, or a wearable configuration of the same (B2, or B2v2). - 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. - Known seizure disorder. |
Country | Name | City | State |
---|---|---|---|
United States | Department of Neurology, Wake Forest School of Medicine | Winston-Salem | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Wake Forest University Health Sciences | The Susanne Marcus Collins Foundation, Inc |
United States,
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* Note: There are 69 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Heart Rate Variability | Heart rate variability is measured in the time domain as standard deviation of beat-to-beat interval (SDNN, milliseconds). For calculation of SDNN, the R-R intervals are visually inspected, and data considered as artifact is manually removed. Heart rate are acquired from 10 minute recordings of noninvasive finger arterial pressure measurements and ECG with participants lying quietly, supine. Systolic BP and beat to beat, RR intervals files generated via the data acquisition system (BIOPAC acquisition system and Acknowledge 4.2 software, Santa Barbara, CA), at 1000 Hz, are analyzed using Nevrokard BRS software (Nevrokard BRS, Medistar, Ljubljana, Slovenia). Analysis is conducted on the first complete 5-minute epoch that is considered to be acceptable for analysis. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Primary | Change in Baroreflex Sensitivity | BRS calculated by this method is based on quantification of sequences of at least three beats (n) in which SBP consecutively increases (UP sequence) or decreases (DOWN sequence), which are accompanied by changes in the same direction of the RRI of subsequent beats (n+1). The software scans the RRI and SBP records, identifies sequences, and calculates linear correlation between RRI and SBP for each sequence. The mean of all individual regression coefficients (slopes), a measure of sequence BRS, is calculated for Sequence UP, DOWN and ALL (ms/mmHg). Blood pressure and heart rate are acquired from 10 minute recordings of noninvasive finger arterial pressure measurements and ECG with participants lying quietly, supine. Systolic BP and beat to beat, RR intervals files generated via the data acquisition system (BIOPAC acquisition system and Acknowledge 4.2 software, Santa Barbara, CA), at 1000 Hz, are analyzed using Nevrokard BRS software (Nevrokard BRS, Medistar, Ljubljana, Slovenia). | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Primary | Change in Blood Pressure | BP measurements will be obtained using an automate oscillometric blood pressure device. Three samples will be obtained and the last two averaged to get the value that will be used as the reading for that visit. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Primary | Change in Blood Pressure Variability | Systolic BP and beat to beat, RR intervals (RRI) files generated via the data acquisition system (BIOPAC acquisition system and software, Santa Barbara, CA) at 1000 Hz are analyzed using Nevrokard SA-BRS software (by Nevrokard Kiauta, d.o.o., Izola, Slovenia) for measures BPV.Frequency Method. Power spectral densities of SBP and RRI oscillations are computed by 512 points Fast Fourier Transform (FFT) and integrated over specified frequency ranges (LF: 0.04-0.15 Hz; HF: 0.15-0.4 Hz). | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in Insomnia Severity Index (ISI) | The severity of insomnia symptoms is measured using the ISI with each data collection visit. The ISI is a 7 question measure, with responses from 0-4 for each question, yielding scores ranging from 0-28. Higher scores indicate the strength of the insomnia severity. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in Pittsburgh Sleep Quality Index (PSQI) | The PSQI is a 19 item inventory that assesses sleep quality over a 1-month time interval. Items are weighted on a 0-3 interval scale. A global PSQI score is calculated by totaling the seven component scores, providing an overall score ranging from 0 to 21, where lower scores denote a healthier sleep quality. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in Center for Epidemiologic Studies Depression Scale (CES-D) | The CES-D is a 20-item survey assessing affective depressive symptomatology to screen for risk of depression. Scores range from 0-60, with a score of 16 commonly used as a clinically relevant cut-off. Higher scores indicate the presence of more symptomatology. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in Generalized Anxiety Disorder-7 (GAD-7) | The GAD-7 is a seven item screening tool for anxiety that is widely used in primary care. Scores range from 0-21. A lower score denotes a lower level of anxiety. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in Perceived Stress Scale (PSS) | The PSS is a ten-item psychological instrument for measuring the perception of stress. It is a measure of the degree to which situations in one's life are appraised as stressful. Scores range from 0-40. A lower score denotes a lower level of perceived stress. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in Quality of Life Scale (QOLS) | The QOLS is a 16-item scale that was modified from a 15-item scale used in chronic disease patients. Topics include different components of daily life such as relationships, community engagement, personal fulfillment, and recreation. Each item is scaled from 1 to 7 and a sum score is calculated to represent higher levels of satisfaction in life (range is 16-112). | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in PTSD Checklist for Civilians (PCL-C) | The PCL-C measures the American Psychiatric Association's Diagnostic and statistical manual of mental disorders (DSM-IV) Criteria B, C, & D of PTSD symptoms based on traumatic life experience related to civilians. Seventeen items are rated on a Likert scale with a composite score range of 17 to 85. A score of 44 or higher correlates with probability of civilian-related PTSD. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in International Physical Activity Questionnaire (IPAQ-SF) | This is a four item questionnaire asking about physical activity in the last 7 days. Scores are calculated and categorized as low, moderate, or high. A higher score denotes more physical activity. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) | |
Secondary | Change in HIRREM Physical Activity Satisfaction Questions | This is a four item questionnaire asking about the participants level of satisfaction with their physical activity. Responses range from 0-6 for each question, yielding scores ranging from 0-24. Higher scores denote a higher level of satisfaction. | Baseline, V2 (0-14 days after final session), and V3 (4-6 weeks after V2) |
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