Evaluation of the Impact of Stress on IVF Outcome
- Conditions
- Stress, PhysiologicalStress, PsychologicalInfertility
- Registration Number
- NCT05589571
- Lead Sponsor
- Inception Fertility Research Institute, LLC
- Brief Summary
The purpose of this study is to determine if physiological measures of stress, measured by the non-invasive OTO device, are significantly correlated with IVF outcome.
- Detailed Description
The OTO device is a wearable device that utilizes multiple methods of electrophysiology to identify the impact of stress on humans. The device consists of the OTO sensor, a belt with two electrode pads worn around the chest, one electrode placed on the thenar of the dominant hand and one electrode placed on the forehead; the sensor pairs with the OTO App via Bluetooth. It tracks 54 physiological properties including temperature, HRV, amplitude frequency analysis (AFA) of ECG and DC potential. This data is analyzed by the proprietary OTO Expert System which creates the overall conclusions on levels of stress, functional reserves, adaptive capacity and level of readiness to additional stressors.
Physiological data will be collected from the study participant using the OTO device for the duration of one IVF and frozen embryo transfer (FET) cycle. Study participants will complete questionnaires online related to perceived stress at the beginning and the end of study participation. Study participant's IVF cycle treatment and outcome data will be collected and analyzed in conjunction with the physiological data collected with the OTO device.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- Female
- Target Recruitment
- 240
- Women age 25-40 years old
- Planning to undergo their first IVF cycle with frozen embryo transfer at one of the participating fertility clinics
- Have access to the internet and own a smartphone
- Ability and willingness to wear the OTO device for a few minutes each morning during their IVF and FET cycle
- Able to read and speak English
- Medical history of cardiac arrhythmias
- History of cardiac surgery within a year of study enrollment
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Physiological Stress 7 weeks Physiological stress will be measured using the non-invasive OTO device, which tracks 54 physiological properties including temperature, hear rate variability (HRV), amplitude frequency analysis (AFA) of electrocardiogram (ECG) and direct current (DC) potential.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (18)
Aspire Houston Fertility Institute - Memorial City
đşđ¸Houston, Texas, United States
Indiana Fertility Institute
đşđ¸Indianapolis, Indiana, United States
Aspire Fertility San Antonio - Sonterra
đşđ¸San Antonio, Texas, United States
Tennessee Fertility Institute
đşđ¸Nashville, Tennessee, United States
IVFMD
đşđ¸Viera, Florida, United States
Reproductive Biology Associates
đşđ¸Marietta, Georgia, United States
Main Line Fertility
đşđ¸West Chester, Pennsylvania, United States
Aspire Houston Fertility Institute - Main Street
đşđ¸Houston, Texas, United States
Aspire Houston Fertility Institute - Willowbrook
đşđ¸Houston, Texas, United States
Aspire Houston Fertility Institute - Medical Center
đşđ¸Houston, Texas, United States
Aspire Fertility McAllen
đşđ¸McAllen, Texas, United States
Aspire Fertility San Antonio - Medical Center
đşđ¸San Antonio, Texas, United States
Aspire Houston Fertility Institute - Piney Point
đşđ¸Houston, Texas, United States
Center for Reproductive Medicine
đşđ¸Winter Park, Florida, United States
Aspire Fertility Dallas
đşđ¸Dallas, Texas, United States
Advanced Fertility Center of Chicago
đşđ¸Gurnee, Illinois, United States
Aspire Houston Fertility Institute
đşđ¸Webster, Texas, United States
Aspire Fertility Austin
đşđ¸Austin, Texas, United States