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NCT ID: NCT04665479 Completed - Pediatrics Clinical Trials

Digital-storytelling Intervention for Rural-dwelling Children

Start date: February 12, 2021
Phase: N/A
Study type: Interventional

The overall purpose of this study is to test the feasibility of a web-based storytelling intervention for rural-dwelling children (ages 8-17) with serious advanced illnesses. There is a growing need for home-based end-of-life and palliative care for children with serious illnesses. While palliative care interventions offered in home settings are significantly lacking, the problems are magnified by substantial gaps in access to palliative care for rural populations. Web-based recruitment and intervention methods have the potential to access hard-to-reach rural populations and provide a cost-effective health care. In particular, legacy-making (i.e., actions/behaviors aimed at being remembered) is one strategy to help decrease suffering and improve psychosocial outcomes for children with serious illness and end of life needs. Storytelling has successfully documented child legacies and may be an ideal format for children. Guided by our existing, web-based digital storytelling intervention and previous work, this project will offer a remotely-delivered legacy-making intervention to rural-dwelling children with diverse serious, advanced health conditions and their parents.

NCT ID: NCT04665323 Completed - Clinical trials for Fibrodysplasia Ossificans Progressiva

An International Cross-sectional Survey to Evaluate the Burden of Fibrodysplasia Ossificans Progressiva (FOP) on Patients and Their Families.

Start date: January 18, 2021
Phase:
Study type: Observational

The FOP burden of illness (BoI) survey aims to assess the impact of the burden of FOP on patients and their families. The study is being conducted online and available for residents in Argentina, Brazil, Canada, France, Germany, Italy, Japan, Mexico, Poland, Russia, South Korea, Spain, Sweden, the US, and the UK.

NCT ID: NCT04665154 Completed - Healthy Volunteers Clinical Trials

A First-in-human Study to Investigate the Safety, Tolerability and Pharmacokinetics of MAS825 in Healthy Volunteers

MAS-FIH
Start date: June 7, 2019
Phase: Phase 1
Study type: Interventional

The study is conducted to investigate the safety, tolerability and pharmacokinetics of MAS825 in healthy volunteers.

NCT ID: NCT04665011 Completed - Heart Failure Clinical Trials

Validation of Indicor Photoplethysmography (PPG) Valsalva Pulse Response vs Non-invasive Blood Pressure

Start date: December 14, 2020
Phase:
Study type: Observational

This study designed is compare the pulse response to the Valsalva maneuver between a photoplethysmography sensor (PPG) and non-invasive blood pressure sensor for the purpose of validating the PPG methodology in deriving a value for the Valsalva pulse response. The aim is to show that the PPG method captures the same phase responses as the blood pressure monitor and the primary outcome is the correlation between pulse amplitude ratios for the pulse at the end of the Valsalva to an average baseline pulse.

NCT ID: NCT04664881 Completed - Clinical trials for Myocardial Infarction

Home Telemonitoring In Patients After Myocardial Infarction

Start date: October 14, 2020
Phase: N/A
Study type: Interventional

This study is being done to determine if taking an electrocardiogram (ECG) by a portable device (SmartHeart) followed by a phone call will improve patient outcomes by early recognition of abnormalities and decrease emergency room visits and hospital readmissions compared to standard therapy alone.

NCT ID: NCT04664855 Completed - Stress Clinical Trials

A Trauma-Informed Approach for Positive Youth Development for Montana Students

Start date: January 15, 2021
Phase: N/A
Study type: Interventional

Given the prevalence of suicide and mental health issues in rural Montana, this project is intended to help mitigate stressors that may contribute to poor behavioral and mental health in high school-aged children. The immediate goal is to measure physical and mental health outcomes in adolescents resulting from a trauma-informed yoga intervention designed to foster positive youth development and student success. It builds on feasibility study for year one in which 19 experimental condition participants engaged in an 8-week yoga program.

NCT ID: NCT04664608 Completed - Epilepsy Clinical Trials

Pediatric EEG Monitoring

Start date: January 1, 2021
Phase:
Study type: Observational

The purpose of this study is to understand if a new, smart, wireless EEG developed by our team can be used to monitor the continuous electrical activity of the brain in the ICU and EMU and whether it works as well as the current standard, wired EEGs.

NCT ID: NCT04664400 Completed - Healthy Clinical Trials

N-of-few Study of Pain Perception

NOF
Start date: January 22, 2021
Phase: N/A
Study type: Interventional

A behavioral study that will examine how pain perception is affected by different types of conditioning and by context, with a few participants and multiple sessions ("N-of-few" design).

NCT ID: NCT04664309 Completed - COVID-19 Clinical Trials

Understanding Immunity to the COVID-19 Vaccines

Start date: March 26, 2021
Phase:
Study type: Observational

The purpose of this study is to test over time immunity to the COVID-19 vaccines. Adults who are receiving COVID-19 vaccines will be invited to participate.

NCT ID: NCT04664205 Completed - Clinical trials for Diabetes Mellitus, Type 1

Isoenergetic High Intensity Interval Training and Moderate Intensity Training in Adults With Type I Diabetes

HI1T
Start date: February 1, 2021
Phase: N/A
Study type: Interventional

Type 1 diabetes (T1D) is associated with increased risk of poor cardiometabolic health. Regular exercise is recommended for optimal management of comorbidities in T1D. Unique barriers to exercise exist for T1D, including fear of hypoglycemia, unpredictable glycemic excursions with exercise, and inadequate knowledge about exercise. Unlike traditional moderate intensity continuous training (MICT) which requires extended periods of time, high intensity interval training (HIIT) requires minimal time (~10 minutes of exercise per session), with the potential to rapidly stimulate mitochondrial biogenesis and metabolism. The extent to which these exercise strategies alter metabolomic signatures of carbohydrate, fat, and amino acid metabolism in T1D is unknown. The overall goal of the proposed project is to identify the acute metabolic effects and physiological modifiers of HIIT compared to MICT and control (CON) using metabolomic profiling and cardiometabolic assessments in 14 adults with T1D. Using a randomized cross-over approach, the primary aim is to compare the metabolomics response immediately post, 1 hr post, and glycemic control through 48 hrs after HIIT, compared to MICT matched for total energy expenditure, versus a no exercise CON. An additional aim will be to characterize the influence of biological sex and physiological outcomes (i.e. body composition, lean mass, visceral fat) on the metabolomics profile of these subjects. Outcomes from the present study, with existing data from our team, will lay the foundation for a larger diet and exercise lifestyle intervention that will ultimately lead to changes in clinical practice to co-manage glycemia and cardiometabolic comorbidities.