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NCT ID: NCT05380635 Completed - Clinical trials for Cutaneous T-Cell Lymphoma/Mycosis Fungoides

PK and ECG Determinations Following 8 Weeks of HyBryte Treatment for Cutaneous T-Cell Lymphoma

Start date: May 9, 2022
Phase: Phase 2
Study type: Interventional

To assess the blood levels of hypericin and any electrocardiogram (ECG) changes during 8 weeks of HyBryte (topical hypericin ointment) photodynamic therapy.

NCT ID: NCT05380505 Completed - Food Choices Clinical Trials

Influence of Facebook Ads on Food Choice

Start date: March 16, 2022
Phase: N/A
Study type: Interventional

This is a randomized trial to examine the influence of race-congruent food marketing on social media among Black and White adolescents.

NCT ID: NCT05380362 Completed - Multiple Sclerosis Clinical Trials

Prospective Randomized Endovascular Therapy in Multiple Sclerosis

PREMiSe
Start date: June 2010
Phase: Phase 1
Study type: Interventional

1. To assess the safety of endovascular therapy (balloon angioplasty) for venous stenoses in MS patients with CCSVI as documented by sonographic (extracranial echocolor-Doppler (ECD) and transcranial color Doppler (TCD) 2. To study the morphology of the venous anomalies by using intraluminal ultrasound (IVUS). 3. To evaluate preliminary efficacy of endovascular therapy (angioplasty) as measured by clinical (relapse rate, disability progression (EDSS)), sonographic (ECD/TCD) and MRI/MRV parameters. 4. To evaluate change in patients self-reported QOL following the therapeutic angioplasty 5. To evaluate whether changes in QOL, fatigue, MSFC or attention following therapeutic angioplasty are associated with brain changes as measured by functional MRI (fMRI).

NCT ID: NCT05380180 Completed - Aging Clinical Trials

Enhancing Quality of Life for Older Adults With and Without Mild Cognitive Impairment (MCI) Through Social Engagement Over Video Technology

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

The goal of this randomized controlled trial is to rigorously assess the efficacy of an 8-week social engagement OneClick intervention. A total of 120 older adults with and without mild cognitive impairment (60 per group) will be randomized after a baseline assessment to the social engagement OneClick intervention group or the waitlist control group. Participants assigned to the intervention group will receive the social engagement OneClick intervention for 8 weeks, and will complete a mid-assessment at week 4, and a post-assessment at week 8. Participants assigned to the waitlist control group will receive no intervention for the first 8 weeks and will complete assessments at week 4 and week 8. Subsequently, as an extension to this study, participants assigned to the waitlist control group will have an opportunity to participate in 8 weeks of social engagement OneClick intervention, with intervention effects assessed at week 4 and week 8.

NCT ID: NCT05380167 Completed - Clinical trials for Cardiovascular Diseases in Old Age

Efficacy Long-term Dietary Nitrate Consumption to Plasma Nitrite Conversion

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

The objective of this study was to determine the chronic effects of beetroot juice supplementation on the acute (90-minute post nitrate consumption) efficacy of converting dietary nitrate to plasma nitrate and plasma nitrite in healthy middle-to-older aged adults. the investigators were also interested in determining the effect of this intervention on fasting levels of plasma nitrate and nitrite over time. Furthermore, the number of participants classified as "non-responders" was determined based on increases in plasma nitrite achieved using tolerable volumes of beetroot juice by other studies.

NCT ID: NCT05380102 Completed - Clinical trials for No Specific Medical Conditions or Disease States

Pilot Evaluation of an Continuous Contactless Vitals Parameter Monitoring System Dozee VS

Start date: April 28, 2022
Phase:
Study type: Observational

The Dozee VS device developed by Turtle Shell Technologies Pvt. Ltd., is a contactless continuous vital parameters monitoring system. It is designed for continuous and contactless measurement of Heart Rate (HR) and Respiratory Rate (RR). The device uses the concept of ballistocardiography and deploys piezoelectric sensors to capture the micro-vibrations originating from cardiac contractions, upper respiratory tract activity and body movements. This data is then analyzed by a proprietary algorithm and the values of the vital parameters - Heart Rate (HR) and Respiratory Rate (RR) are generated. The captured vital parameters can be accessed remotely via a dashboard which can be accessed on any web browser and a smartphone application. The sensor sheet is placed below the mattress and captures data while the user is resting or sleeping and does not require a sensor to be fixed to the body. It consists of the following sub - units: Contactless sensor sheet, Dozee Pod with power cord, 5 Volt Universal Serial Bus (USB) Power Adapter, Health data compute server and Web Dashboard/Mobile App. This provides a more comfortable solution for long-term continuous patient monitoring. Continuous monitoring of people's vital signs, in particular Heart Rate (HR) and Respiratory Rate (RR), may provide a mechanism to alert doctors or nurses of clinical deterioration. Monitoring people's vital signs outside an ICU often relies on nursing staff conducting checks at set intervals. The device can reduce the workload for nursing staff in non-ICU wards.

NCT ID: NCT05379959 Completed - Motivation Clinical Trials

Effects of Stimulants on Behavioral and Neural Markers of Social Motivation, Ability, and Neural Markers of Social Function

MASM
Start date: May 11, 2022
Phase: Early Phase 1
Study type: Interventional

To study the effects of MDMA, compared to a prototypical stimulant, on social motivation, social ability, and neural indices of social function in healthy volunteers

NCT ID: NCT05379933 Completed - Quality of Life Clinical Trials

Caregiver Protocol for Remotely Improving, Monitoring, and Extending Quality of Life

C-PRIME
Start date: May 11, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to test an intervention to improve health promoting behaviors in family caregivers of patients receiving cancer therapy

NCT ID: NCT05379920 Completed - Concussion, Brain Clinical Trials

Salivary Biomarkers for Concussion Recovery

Start date: March 22, 2022
Phase: N/A
Study type: Interventional

The overarching purpose of this proposed research is to determine whether BDNF and/or specific miRNAs can serve as biomarkers for recovery from a concussion during prescribed exercise. The investigators hypothesize salivary BDNF and specific miRNA signatures will change in a statistically significant manner as participants proceed from injury to recovery and participants who show recovery in ANS regulation will show significant differences in salivary BDNF and specific miRNA expression. This study also aims to determine if BDNF and/or specific miRNA can serve as biomarkers of the return of ANS function in concussed patients. The basic premise here is that the volume of exercise will significantly affect the rate of change in the expression of salivary BDNF and miRNA from injury to recovery.

NCT ID: NCT05379881 Completed - Depression Clinical Trials

Efficacy of COMET on Prolific Participants

COMET-Prol
Start date: July 5, 2022
Phase: N/A
Study type: Interventional

In this study, the investigators will test the effectiveness of a digital, single-session mental health intervention. There will be two conditions: the COMET intervention and the control group. The program, COMET (Common Elements Toolbox), will include a variety of modules which will focus on cognitive restructuring, gratitude, behavioral activation, and self-compassion. A similar intervention has previously been tested with Indian adolescents and adapted for US graduate students.