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Biostrap/Apollo Device Use for Heart Rate Variability
N/A
Waitlist Available
Research Sponsored by Joseph Maroon
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Neurosurgical Resident (UPMC)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, two month. analyzed via paired t-test and assessing change between each outcome time point
Awards & highlights
Study Summary
This trial will compare the stress levels of neurosurgery residents with and without the addition of a device that modulates heart rate variability.
Eligible Conditions
- Heart Rate Variability
- Stress
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, two month. analyzed via paired t-test and assessing change between each outcome time point
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, two month. analyzed via paired t-test and assessing change between each outcome time point
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change from baseline to two month Perceived Stress Scale
Change from baseline to two month Quick Inventory of Depressive Symptomatology (QIDS)
Change from baseline to two month heart rate variability
Trial Design
1Treatment groups
Experimental Treatment
Group I: Biostrap/Apollo Device UseExperimental Treatment1 Intervention
Participants wear a Biostrap wearable device which measures steps, heart rate, heart rate variability, sleep metrics, and quantitative data in typical day-to-day activities of residents. Participants then again wear Biostrap except now also with the Apollo device which is worn around the ankle and is suggested to modulate heart rate variability and perceived stress of participants.
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Who is running the clinical trial?
Apollo NeuroUNKNOWN
Joseph MaroonLead Sponsor
Frequently Asked Questions
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