Epileptiform Activity Clinical Trial
Official title:
Sensitivity and Specificity of Mainstream Sleep Tracking Devices Compared to Polysomnography
| Verified date | April 2017 |
| Source | New York University School of Medicine |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to compare two popular portable sleep monitoring devices—the Fitbit Charge®, Jawbone UP®, and SleepTime smartphone app—to the "gold standard" Polysomnography (PSG). Parameters that will be analyzed include sleep onset latency, sleep efficiency, and sleep staging. Specifically, this study will investigate the validity of the Jawbone UP®, Fitbit Charge®, and SleepTime app in detecting sleep and wakefulness in comparison to conventional Polysomnography (PSG).
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | April 2017 |
| Est. primary completion date | April 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Patients undergoing Polysomnography Exclusion Criteria: - severe sleep apnea - severe insomnia with less than two hours of sleep per night - epileptiform activity - electrical status epilepticus of sleep |
| Country | Name | City | State |
|---|---|---|---|
| United States | New York University School of Medicine | New York | New York |
| Lead Sponsor | Collaborator |
|---|---|
| New York University School of Medicine |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Time it takes subject to fall asleep | Up to 3 Months | ||
| Primary | Number of Minutes of Sleep | Up to 3 Months | ||
| Primary | Number of Arousals | Up to 3 Months |