Bioboosti Device for Insomnia Treatment

Completed · Not applicable

Conditions studied: Insomnia

In brief

The purpose of this study is to determine the effects of the Bioboosti device on sleep for patients who have been diagnosed with insomnia.

Key facts

Study ID

NCT02924116

Run by

Brigham and Women's Hospital

People needed

20

Starts

2016-09-01

Expected to finish

2025-04-01

Last updated by the study team

2026-03-04

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with insomnia

You may not qualify if…

• Untreated moderate or severe sleep apnea
• Major circadian rhythm disorder
• Pregnant women
• Breastfeeding
• Cardiac pacemaker
• Cancer
• Severe conditions related to heart, brain, kidney and hematopoietic system
• Severe/unstable angina pectoris
• Arteria coronaria/ peripheral arterial bypass graft
• Acute congestive heart failure
• Renal insufficiency
• Mechanical intestinal obstruction
• Any electrical devices

Where it is running

• Brigham and Women's Hospital — Boston, Massachusetts, United States
• Brigham and Women's Faulkner Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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