Clinical trials: Wearable Devices
Sleep Quality
Understanding Physiology During Float-REST and the Consequential Effects on Subjective and Objective Recovery
The objective of this research study is to assess how the implementation of various modern strategies for augmented recovery and physiological monitoring via wearable biotechnologies and subjective measurements affect sleep…
- Trial name
- NCT04415970
- Testing
- Flotation therapy sensory deprivation tank, Sleep Pod
- Where
- United States
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- West Virginia University
Sleep Apnea
Validation of Sleep Apnea Diagnosis Device
Obstructive sleep apnea (OSA) is common and largely underdiagnosed disease. The standard method for the diagnosis of OSA is a complete night polysomnography (PSG). Simple methods for OSA diagnosis are necessary.
- Trial name
- NCT03526133
- Testing
- Polysomnography (PSG) and wireless sensor Oxistar
- Where
- Brazil
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- University of Sao Paulo General Hospital
Breast Cancer Female, Survivorship
Nurse-led Physical Activity Program Among Breast Cancer Survivors
A nurse-led physical activity program including an individualized exercise program using wearable technology and health coaching based on Social Cognitive Theory will be implemented for women surviving cancer.
- Conditions
- Breast Cancer Female, Survivorship, Health Behavior
- Trial name
- WATSOCPAP (NCT06248918)
- Testing
- WATSOCPAP
- Where
- Turkey (Türkiye)
- Volunteers
- 84 people, healthy volunteers welcome
- Sponsor
- Istanbul Medipol University Hospital
Hypertension, Blood Pressure Monitoring
Wearable Blood-Pressure Monitoring Comparison Study
The goal of this clinical trial is to compare the accuracy, clinical applicability, and usability of different wearable blood pressure monitoring methods integrated in wearable devices, such as smartwatches, in hospitalized…
- Conditions
- Hypertension, Blood Pressure Monitoring, Wearable Devices, Photoplethysmography
- Trial name
- WBPMCS (NCT07719660)
- Where
- 2 sites in Germany, Italy
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Technische Universität Dresden
Healthy Participants
A Sub Study to Evaluate the Study Medication (Etrasimod) Using Wearable Sensors in Healthy Participants
The purpose of this study is to look at how healthy adults process Etrasimod when assessed by wearable sensors. Etrasimod is taken without food and assessments taken by site staff and then by participants after training.
- Trial name
- NCT06140290
- Testing
- Etrasimod Immediate Release (IR)
- Where
- Belgium
- Volunteers
- 8 people, healthy volunteers welcome
- Sponsor
- Pfizer
Medical Device Complication, Brain Injuries
Transcranial Doppler Using Wearable Ultrasound Patch
The main objective of this research is to measure the Doppler signal by the ultrasonic patch. Blood flow measurement is critical for vasospasm, stroke, and embolism monitoring on patients in the ICU or understanding the…
- Conditions
- Medical Device Complication, Brain Injuries, Brain Diseases, Stroke
- Trial name
- TCD (NCT06073145)
- Testing
- conventional transcranial Doppler probe and wearable ultrasound patch.
- Where
- United States
- Volunteers
- 36 people, healthy volunteers welcome
- Sponsor
- University of California, San Diego
Covid19, Stress
Stress and Recovery in Frontline COVID-19 Workers
The novel coronavirus (COVID-19) pandemic has caused an unprecedented stress on healthcare systems in affected countries, and in particular, on the healthcare workers at the frontline working directly with COVID-19 positive…
- Conditions
- Covid19, Stress, Wearables
- Trial name
- NCT04713111
- Testing
- Lifestyle (Meditation), Lifestyle (Exercise)
- Where
- United States
- Volunteers
- 383 people, healthy volunteers welcome
- Sponsor
- 4YouandMe
Major Depressive Disorder, Mood Disorders
Clinical Validation of Samsung Smartwatch
Objective: Wearable technology holds promising potential for mental health monitoring and detection. Samsung has developed an algorithm that they believe can detect signs of depression and anxiety in smartwatch users.
- Conditions
- Major Depressive Disorder, Mood Disorders, Mental Health Issue
- Trial name
- NCT05767593
- Testing
- Wearing Samsung smartwatch and filling out daily surveys
- Where
- United States
- Volunteers
- 220 people, healthy volunteers welcome
- Sponsor
- Massachusetts General Hospital
Insomnia, Sleep Initiation and Maintenance Disorders
Assessment of Smartwatch SAMSUNG to Monitor Sleep Quality: an Observational Prospective Study - SleepEx2 Protocol
The goal of this study is to learn if a smartwatch is effective to identify factors related to sleep quality and habits of adults (30 years old or more), enabling the improvement and/or creation of instruments to assess overall…
- Conditions
- Insomnia, Sleep Initiation and Maintenance Disorders, Health Status, Wearable Electronic Devices
- Trial name
- SLEEP-EX2 (NCT06363656)
- Testing
- Wears the smartwatch during the sleep time to capture sleep characteristics and answer questionaires
- Where
- Brazil
- Volunteers
- 158 people, healthy volunteers welcome
- Sponsor
- University of Sao Paulo General Hospital
Burnout
Vital Coach: A Study of Resiliency in Medical Students
Medical students often begin training with psychological and physiological health metrics superior to their age-matched peers. By graduation, however, rates of depression, anxiety, and physiologic dysregulation are markedly…
- Trial name
- NCT07342673
- Testing
- Arena Strive
- Where
- United States
- Volunteers
- 36 people, healthy volunteers welcome
- Sponsor
- Wake Forest University Health Sciences
Chronic Obstructive Pulmonary Disease
Utilizing Wearable Device to Observe the Clinical Response of COPD Patients Treated With Combined Bronchodilator and Home-based Pulmonary Rehabilitation Program
The effectiveness of combined bronchodilator and exercise training on improving exercise capacity has been reported in COPD. However, little is known about effect of respective treatment in a real-time monitoring.
- Trial name
- NCT03364829
- Testing
- Indacaterol/Glycopyrronium
- Where
- Taiwan
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Taipei Medical University Shuang Ho Hospital
Spinal Cord Injuries, Tetraplegia
MyHand-SCI: An Active Hand Orthosis for Spinal Cord Injury
The purpose of this study is to develop and test the hardware and software components of the MyHand-SCI device to assist with hand function for individuals with C6-C7 spinal cord injury.
- Trial name
- NCT05553457
- Testing
- Testing of MyHand-SCI Device
- Where
- United States
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Columbia University
Pregnancy Related
Feasibility of Using NeoSpot at Community Settings
Continuous vital sign monitoring is a basic tenet of specialized care in the developed world that is vastly underutilized during hospital or clinic admissions or outpatient routine visits in most low-and-middle income countries…
- Trial name
- NCT05652777
- Testing
- NeoSpot
- Where
- Zambia
- Volunteers
- 149 people, healthy volunteers welcome
- Sponsor
- Centre for Infectious Disease Research in Zambia
Digital Health Intervention, Remote Consultation, Teleconsultation
Evaluation and Implementation of Digital Health Ecosystem in Academic Health Center
Mobile health technologies, such as smartwatches, wearable sensors, and digital applications, have the potential to support healthier lifestyles and improve the management of health conditions.
- Conditions
- Digital Health Intervention, Remote Consultation, Teleconsultation, Lifestyle Factors, Stress
- Trial name
- e-IDEA (NCT07831837)
- Testing
- Integrated Digital Health Ecosystem, Usual Primary Care
- Where
- 2 sites in Canada
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Laval University
Parkinson Disease (PD), Healthy (Controls)
Clinical Validity of the DANU Sports System for Gait and Balance Assessment in Parkinson's Disease
This observational study aims to explore the use of the DANU Smart Socks for gait and balance assessment in people with Parkinson's (PwP).
- Trial name
- NCT07281794
- Where
- 2 sites in United Kingdom
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Northumbria University
Blood Loss, Surgical, Postoperative Hemorrhage
Study of the Hemorai Vysio Wearable Device for Monitoring Changes Related to Blood Loss in Patients During and After Surgery.
The goal of this clinical trial is to learn whether the Hemorai Vysio wearable device can be used safely and feasibly to track relative changes over time in tissue oxygen, hemoglobin-related signals, blood flow, and oxygen use…
- Trial name
- VYSIO-FEASIBIL (NCT07826637)
- Testing
- Wearable optical hemodynamic monitoring device
- Where
- United States
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Hemorai Inc
Sleep
Enhancement of Sleep With Wearables
Sleep, specifically deep sleep, plays a central role in healthy brain function, cardio-vascular processes, mood and quality of life.
- Trial name
- WESA (NCT03420677)
- Testing
- Application of tones, No application of tones
- Where
- Switzerland
- Volunteers
- 33 people, healthy volunteers welcome
- Sponsor
- Swiss Federal Institute of Technology
Circadian Rhythm
Circadian Rhythm Monitoring Study
This will be a single-center, prospective observational study designed to evaluate the feasibility and accuracy of a new wearable device for non-invasive continuous monitoring of physiological signals to derive circadian rhythm.
- Trial name
- NCT07336654
- Testing
- Circadian monitoring device
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- ResMed
Respiratory Rate Monitoring
Validation of Respiratory Rate Measurement Accuracy Using a Smartwatch
This prospective study evaluates the accuracy of commercial wearable devices by comparing their respiratory rate measurements against clinical standards like spirometers and ECGs in healthy adults.
- Trial name
- BREATHWATCH (NCT07578389)
- Testing
- Respiratory rate monitoring using wearable device
- Where
- Czechia
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Czech Technical University in Prague
Physical Activity, Poor Quality Sleep
SMART Technology to Promote Heart Health in Midlife Adults
This study aims to increase weekly minutes of moderate-to-vigorous physical activity and improve sleep quality in a sample of mid-life adults between ages 50 and 64 years.
- Conditions
- Physical Activity, Poor Quality Sleep, Hypertension
- Trial name
- BeSMART (NCT03724474)
- Testing
- Be SMART
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- University of Delaware