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NCT ID: NCT05119192 Completed - Amputation Clinical Trials

Dual-tasking for Individuals With Lower Limb Amputation: Exploring the Relationship to Falls and Instrumental Activities of Daily Living

DIAL
Start date: December 1, 2021
Phase:
Study type: Observational

Veterans with dysvascular lower limb amputation (LLA) have a high fall risk, which persists despite completion of conventional rehabilitation. The presence of fall risk could be a primary reason for the high disability and low quality of life outcomes in this Veteran population. A potential novel intervention for this population is to train performance of tasks that require both physical and cognitive attention (i.e., dual-tasking). Therefore, the purpose of this study is to explore relationships between dual-task performance and self-reported falls for Veterans with dysvascular LLA. Further, dual-tasking occurs during everyday life and this project will examine the association between dual-task performance and participation in activities of daily living (basic and instrumental). The results will form the foundation for development and future study of a novel dual-task training program for Veterans with dysvascular LLA.

NCT ID: NCT05119153 Completed - Hyperglycemia Clinical Trials

Effects of Coffee Roasting on Blood Sugar Levels in Healthy Humans

Start date: November 5, 2019
Phase: N/A
Study type: Interventional

The present study determined the effects light, medium, and dark roasted, brewed coffees on blood glucose responses in normal (n = 19) subjects.

NCT ID: NCT05119127 Completed - Cataract Clinical Trials

Rotational Stability of Acrysof IQ Vivity Extended Vision Toric IOL and Refractive Visual Outcome.

Start date: September 30, 2020
Phase: N/A
Study type: Interventional

The purpose of this research is to assess the rotational stability of the AcrySof IQ Vivity Extended Vision Toric IOL and Refractive Visual outcome.

NCT ID: NCT05119023 Completed - Aphasia Clinical Trials

Determining Learning Ability in People With Aphasia

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

Aphasia is an impairment in the expression or comprehension of language that results from stroke, traumatic brain injury or progressive neurological disease. Approximately two million people in the United States suffer from aphasia, which has profound impacts on quality of life, the ability to return to work and participation in life activities. Research has shown that speech-language therapy, the treatment for aphasia, can significantly improve people's ability to communicate. However, a major limitation in the field of aphasia rehabilitation is the lack of predictability in patients' response to therapy and the inability to tailor treatment to individuals. Currently, aphasia treatments are selected largely based on patient's language abilities and language deficits with little consideration of learning ability, which this study refers to as learning phenotype. Learning phenotype has been used to inform rehabilitation approaches in other domains but is not currently considered in aphasia. The overarching hypothesis of this work is that poor alignment of learning ability and language therapy limits progress for patients and presents a barrier to individualizing treatment. The objectives of the proposed study are to (1) determine the learning phenotype of individuals with aphasia, and (2) examine how lesion characteristics (size and location of damage to the brain), language ability and cognitive ability relate to learning ability. To accomplish objectives, investigators propose to measure implicit (observational) and explicit (rule-based) learning ability in people with aphasia via computer-based tasks. Regression models will be used to examine brain and behavioral factors that relate to learning ability.

NCT ID: NCT05118802 Completed - Clinical trials for Malignant Solid Neoplasm

Measuring the Impact of MANNA s Medically Tailored Meal Program in Patients With a Non-terminal Cancer Diagnosis

Start date: August 11, 2021
Phase:
Study type: Observational

This study identifies patient-important outcome measures and develops a survey that assesses the impact of nutritional interventions among cancer patients. Currently, data on the impact of medically tailored meals on outcomes that are meaningful to patients, providers, and payers are limited. For this reason, access to medically tailored meals as a covered benefit for cancer patients is limited. Thus, there is a need to explore the efficacy of nutritional interventions among this population. This study identifies outcome measures for nutritional interventions that are meaningful to patients and providers.

NCT ID: NCT05118750 Completed - Clinical trials for Major Depressive Disorder

ALTO-300 in Depression

Start date: December 13, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to collect biologically-based data for defining predictors and correlates of the effects of ALTO-300.

NCT ID: NCT05118516 Completed - Healthy Volunteer Clinical Trials

Safety, Tolerability, and Pharmacokinetics of ASC43F, a Fixed Dose Combination Tablet in Healthy Subjects

Start date: November 1, 2021
Phase: Phase 1
Study type: Interventional

This is a phase 1, open-label study in healthy adults. This study is aimed at evaluating the safety, tolerability, and pharmacokinetics of ASC43F, a fixed-dose combination (FDC) and single dose tablet containing ASC41, a THR β agonist and ASC42, an FXR agonist in healthy subjects.

NCT ID: NCT05118503 Completed - Stroke Clinical Trials

Personalized Patient and Caregiver Education After Stroke

MyStroke
Start date: October 20, 2021
Phase: N/A
Study type: Interventional

This is a randomized pilot trial to evaluate the impact of a customizable stroke education app (vs standard of care discharge education) on patient satisfaction and education retention. The impact of the intervention will be assessed 7, 30, and 90 days post-discharge.

NCT ID: NCT05118386 Completed - RSV Infection Clinical Trials

Safety, Tolerability, and Pharmacokinetics of RSV Monoclonal Antibody RSM01 in Healthy Adults

Start date: November 16, 2021
Phase: Phase 1
Study type: Interventional

Gates MRI-RSM01-101 was a Phase 1, randomized, double-blind, placebo-controlled, dose-escalation study to evaluate the safety and tolerability, pharmacokinetics, occurrence of Anti-drug antibody (ADA), and assessment of neutralizing antibody against RSV after administration of single intravenous or intramuscular doses of RSM01 to healthy adults.

NCT ID: NCT05118191 Completed - Sleep Quality Clinical Trials

Efficacy of Commercially Available Technology in Augmenting Sleep and Well-being

Start date: October 18, 2021
Phase: N/A
Study type: Interventional

The objective of this research study is to assess how the implementation of various commercially available devices affect sleep quality, sleep structure, nocturnal physiology, subjective wellness, recovery from stressors, and resultant effects on performance and well-being.