Sleep Clinical Trial
— RESTOfficial title:
Resilience to Sleep Deprivation and Changes in Sleep Architecture in Shoonya Meditators
This study aims to investigate the effect of a 15-minute meditation practice on sleep architecture and high-frequency Heart Rate Variability (HF-HRV), as well as cognitive performance after both a well-rested and sleep-deprived night.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: 1. Shoonya meditation program participants/individuals eligible to participate who are healthy adults of age 18 or older, and reside in the United States. Participants must be able and willing to travel to Boston. 2. Nap Group: Healthy adults of age 18 or older that reside in the United States, nap regularly (at least 3 times a week), and do not meditate regularly. Exclusion Criteria: 1. History of any neurological condition (i.e. Parkinson's disease, Alzheimer's disease, Huntington's disease, brain tumors, brain surgery, or multiple sclerosis) 2. History of any psychiatric disorder, within last 5 years (i.e. anxiety, psychosis, posttraumatic stress disorder, attention deficit hyperactive disorder) 3. Current use of cognition enhancing medications 4. Active history (within the last 5 years) of alcohol or drug abuse (> 10 drinks per week) 5. History (within the last 5 years) of stroke/aneurysm 6. Recent history (< 3 months) of seizures 7. 60 years of age or older 8. History of Heart Attack and Ejection Fraction less than or equal to 30% 9. Pregnancy 10. Non-English speaking 11. History/Diagnosis of any sleep disorder 12. Consumption of 3 or more cups of coffee a day 13. Previously learned shoonya meditation (for the meditator groups) |
Country | Name | City | State |
---|---|---|---|
United States | Beth Israel Deaconess Medical Centre | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Beth Israel Deaconess Medical Center |
United States,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Error frequency Change: Go-No Go Task | The primary outcome is the difference in number of commission and omission errors on the Go-No Go task. The difference in scores pre- and post-sleep deprivation will be analyzed between the control and intervention group. | 2 months post learning meditation | |
Secondary | Reaction Time Change: Go-No Go | The difference in reaction times on the Go-No Go task. The difference in scores pre- and post-sleep deprivation will compared between the control and intervention groups. | 2 months post learning meditation |
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