Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who provide at least 10 hours of caregiving per week (any type of caregiving counts)
- People who are willing to give their informed consent to participate
- People who are able to follow basic instructions
- People who are able to sit comfortably for up to 90 minutes and attend up to three 60-minute sessions per week over a 4-week period
- People who report experiencing stress, anxiety, or sleep problems, and whose symptoms reach a certain level on at least one of the study's standard questionnaires (confirm with trial site for exact score thresholds)
Who may not be able to join:
- People who provide fewer than 10 hours of caregiving per week
- People who are unable or unwilling to attend the sessions during the study period
- People who are unable or unwilling to give their consent to participate
- People who are not experiencing symptoms of stress, anxiety, or insomnia
- People with a hearing impairment severe enough that they cannot hear tones through earbuds
- People with a known seizure disorder, or who have had thoughts of suicide in the last 3 months
- People who weigh more than 400 pounds (due to the weight limit of the chair used in the study)
- People who are currently taking part in another intervention study
- People who have used the specific technology being tested in this trial within the past 3 years
- People who have used certain brain or nervous system therapies — such as neurofeedback, biofeedback, deep brain stimulation, EMDR, electroconvulsive therapy, or similar treatments — within the last month
- People with a pacemaker, or who take medications (such as beta blockers) that may affect heart rate measurements
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Charles Tegeler, MD, Wake Forest University Health Sciences
Phone: 336-716-9447
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in Blood Pressure Measurements; Change in Heart Rate (HR); Change in Heart Rate Variability (HRV); Change in Baroreflex Sensitivity; Blood Pressure Variability
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.