CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 20 enrolled
Drug / intervention
Bioboostidevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02924116
NCT02924116N/ACompleted

Use of Bioboosti Non-pharmacologic Device for Insomnia Treatment: A Pilot Study

Brigham and Women's Hospital·interventional·Posted Oct 5, 2016·Updated Mar 4, 2026

In Brief

A clinical study evaluating Bioboosti for Insomnia. Completed, enrolled 20 participants across 2 sites.

Detailed Summary

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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsInsomnia
CountriesUnited States

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedOct 5, 2016
Enrollment StartSep 1, 2016
Primary CompletionNov 1, 2024
Study CompletionApr 1, 2025
TodayJul 2, 2026
Enrollment to primary: 8.2 yearsPosted 9.7 years ago

Interventions

Bioboostidevice

Subjects will place the device on the palm of their hand for 8 minutes. There is a light on the device that changes to indicate that the 8 minutes have passed. They will then place it on the palm of the other hand and keep it there for 8 minutes. Alternating 8-minute cycles between hands will be done up to 6 times.