Trial Outcomes & Findings for Bioboosti Device for Insomnia Treatment (NCT NCT02924116)

NCT ID: NCT02924116

Last Updated: 2026-03-04

Results Overview

Change in Insomnia Severity Index (ISI) will be measured. The Insomnia Severity Index (ISI) is a short, 7-item self-report questionnaire used to screen for insomnia, assess its severity, and monitor treatment effectiveness by evaluating sleep problems (like falling/staying asleep, early waking) and their impact on daytime functioning over the past two weeks. Scoring from 0 to 28, with higher scores indicating greater severity, the ISI helps classify insomnia as none, subthreshold, moderate, or severe, guiding clinical decisions in research and practice. This will be done before and after treatment.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

20 participants

Primary outcome timeframe

Baseline to 2 weeks

Results posted on

2026-03-04

Participant Flow

Bioboosti arm was only arm to enroll. No participants were enrolled in the "sustained efficacy" or "insomnia and migraine arms" as seen in results section and study publication

Participant milestones

Participant milestones
Measure
Bioboosti
Treatment with the Bioboosti device for two weeks. The device produces a pulsed micro-magnetic field. Subjects will use it once a day for about one hour, before habitual sleep time.
Sustained Efficacy
Treatment with Bioboosti device for a year. In order to see if the device has sustained efficacy in treating insomnia. Subjects will use it once a day for about one hour, before habitual sleep time.
Insomnia and Migraine
Treatment with the Bioboosti device for a month. Subjects will use it once a day for about one hour, before habitual sleep time.
Overall Study
STARTED
20
0
0
Overall Study
COMPLETED
17
0
0
Overall Study
NOT COMPLETED
3
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Race and Ethnicity were not collected from any participant.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Bioboosti
n=20 Participants
Treatment with the Bioboosti device for two weeks. The device produces a pulsed micro-magnetic field. Subjects will use it once a day for about one hour, before habitual sleep time.
Sustained Efficacy
Treatment with Bioboosti device for a year. In order to see if the device has sustained efficacy in treating insomnia. Subjects will use it once a day for about one hour, before habitual sleep time.
Insomnia and Migraine
Treatment with the Bioboosti device for a month. Subjects will use it once a day for about one hour, before habitual sleep time.
Total
n=20 Participants
Total of all reporting groups
Age, Categorical
<=18 years
0 Participants
n=20 Participants
0 Participants
n=20 Participants
Age, Categorical
Between 18 and 65 years
18 Participants
n=20 Participants
18 Participants
n=20 Participants
Age, Categorical
>=65 years
2 Participants
n=20 Participants
2 Participants
n=20 Participants
Age, Continuous
45.6 Years
STANDARD_DEVIATION 17.1 • n=20 Participants
45.6 Years
STANDARD_DEVIATION 17.1 • n=20 Participants
Sex: Female, Male
Female
14 Participants
n=20 Participants
14 Participants
n=20 Participants
Sex: Female, Male
Male
6 Participants
n=20 Participants
6 Participants
n=20 Participants
Race and Ethnicity Not Collected
0 Participants
Race and Ethnicity were not collected from any participant.
Region of Enrollment
United States
20 participants
n=20 Participants
20 participants
n=20 Participants

PRIMARY outcome

Timeframe: Baseline to 2 weeks

Population: Study only managed to progress to Bioboosti Arm, and not the other arms. Of the 20 enrolled patients, only 17 completed all necessary testing and were therefore included in data analysis.

Change in Insomnia Severity Index (ISI) will be measured. The Insomnia Severity Index (ISI) is a short, 7-item self-report questionnaire used to screen for insomnia, assess its severity, and monitor treatment effectiveness by evaluating sleep problems (like falling/staying asleep, early waking) and their impact on daytime functioning over the past two weeks. Scoring from 0 to 28, with higher scores indicating greater severity, the ISI helps classify insomnia as none, subthreshold, moderate, or severe, guiding clinical decisions in research and practice. This will be done before and after treatment.

Outcome measures

Outcome measures
Measure
Bioboosti
n=17 Participants
Treatment with the Bioboosti device for two weeks. The device produces a pulsed micro-magnetic field. Subjects will use it once a day for about one hour, before habitual sleep time.
Sustained Efficacy
Treatment with Bioboosti device for a year. In order to see if the device has sustained efficacy in treating insomnia. Subjects will use it once a day for about one hour, before habitual sleep time.
Insomnia and Migraine
Treatment with the Bioboosti device for a month. Subjects will use it once a day for about one hour, before habitual sleep time.
Insomnia Severity Index
5.4 Scores on a scale
Standard Deviation 4.5

PRIMARY outcome

Timeframe: Baseline to 2 weeks

Population: Study only managed to progress to Bioboosti Arm, and not the other arms. Of the 20 enrolled patients, only 17 completed all necessary testing and were therefore included in data analysis.

The change in the Pittsburgh Sleep Quality Index (PSQI) from baseline to 2 weeks will be measured. The PSQI is a widely used, self-rated questionnaire that assesses sleep quality and disturbances over a one-month period. It consists of 19 items that generate seven component scores (subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction), which are summed to yield a global score ranging from 0 to 21. Higher global scores indicate worse sleep quality. Change will be calculated as the PSQI score at 2 weeks minus the PSQI score at baseline (Week 2 - Baseline). Because lower PSQI scores indicate better sleep quality, a negative change score reflects an improvement in sleep quality, whereas a positive change score reflects worsening sleep quality.

Outcome measures

Outcome measures
Measure
Bioboosti
n=17 Participants
Treatment with the Bioboosti device for two weeks. The device produces a pulsed micro-magnetic field. Subjects will use it once a day for about one hour, before habitual sleep time.
Sustained Efficacy
Treatment with Bioboosti device for a year. In order to see if the device has sustained efficacy in treating insomnia. Subjects will use it once a day for about one hour, before habitual sleep time.
Insomnia and Migraine
Treatment with the Bioboosti device for a month. Subjects will use it once a day for about one hour, before habitual sleep time.
Pittsburgh Sleep Quality Index
4.1 Score on a scale
Standard Deviation 3.4

PRIMARY outcome

Timeframe: Baseline to 2 weeks

Population: Study only managed to progress to Bioboosti Arm, and not the other arms. Of the 20 enrolled patients, only 17 completed all necessary testing and were therefore included in data analysis.

Daytime sleepiness will be assessed using a Visual Analog Scale (VAS) from baseline to 2 weeks. The VAS is a subjective measure consisting of a 100 mm horizontal line anchored by "not at all sleepy" (0 mm) on the left and "extremely sleepy" (100 mm) on the right. Participants mark the point on the line that best represents their current level of daytime sleepiness. Higher scores indicate greater sleepiness. Change will be calculated as the VAS score at 2 weeks minus the VAS score at baseline (Week 2 - Baseline). Because higher scores indicate greater sleepiness, a negative change score reflects a reduction in daytime sleepiness (improvement), whereas a positive change score reflects an increase in daytime sleepiness (worsening). The mean change and standard deviation of the change scores will be reported.

Outcome measures

Outcome measures
Measure
Bioboosti
n=17 Participants
Treatment with the Bioboosti device for two weeks. The device produces a pulsed micro-magnetic field. Subjects will use it once a day for about one hour, before habitual sleep time.
Sustained Efficacy
Treatment with Bioboosti device for a year. In order to see if the device has sustained efficacy in treating insomnia. Subjects will use it once a day for about one hour, before habitual sleep time.
Insomnia and Migraine
Treatment with the Bioboosti device for a month. Subjects will use it once a day for about one hour, before habitual sleep time.
Daytime Sleepiness
1.7 Score on a scale
Standard Deviation 2.8

Adverse Events

Bioboosti

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Sustained Efficacy

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Insomnia and Migraine

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Milena Pavlova, M.D.

Brigham and Women's Hospital

Phone: (617) 983-7580

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place