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NCT ID: NCT04612868 Completed - Diabetes Mellitus Clinical Trials

Efficacy and Safety of AEYE-DS Software Device for Automated Detection of Diabetic Retinopathy From Digital Fundus Images

Start date: October 16, 2020
Phase: N/A
Study type: Interventional

AEYE-DS is a software device developed to increase compliance with diabetic retinopathy screening by automatically detecting more-than-mild diabetic retinopathy from digital fundus images using Artificial Intelligence (AI)-based software. This study has been designed to validate the safety and efficacy of the device at primary care and other point of care sites.

NCT ID: NCT04612842 Completed - Behavior Clinical Trials

Engaging Older Adults in Fall Prevention Using Motivational Interviewing (MI)

Start date: September 9, 2020
Phase: N/A
Study type: Interventional

This mixed-methods, two-arm, randomized controlled trial will evaluate the impact of Motivational Interviewing (MI) as a follow-up care to patients who received fall prevention recommendations at Oregon Health & Science University Internal Medicine and Geriatrics Clinic provided over 12 months.

NCT ID: NCT04612660 Completed - Cervical Cancer Clinical Trials

HPV Self-test to Increase Cervical Cancer Screening in Asian Women

Start date: September 2014
Phase: N/A
Study type: Interventional

The study was to pilot test the feability of using HPV self-sampling testing to increase cervical cancer screening among under-served Asian women through engaging community-based organizations in the greater Philadelphia and New York City area, addressing a significant global cancer burden, the preventable infection-related cervical cancer.

NCT ID: NCT04612647 Completed - Clinical trials for Autism Spectrum Disorder

Fit Families Program: Fundamental Motor Skill Intervention in Children With Autism Spectrum Disorders and Their Parents

Start date: January 2, 2020
Phase: N/A
Study type: Interventional

The investigators aim to identify the effect of a 12-week fundamental motor skills (FMS) (e.g., throwing, catching, running) intervention on the active participation in physical recreation activities and a variety of other factors (child behaviors, communication, and adaptive skills) and to identify patterns, benefits, constraints, and strategies to active participation in physical recreation activities among families of children with autism spectrum disorders (ASD) (pre-post) through in-person or via phone interviews with parents and children with ASD.

NCT ID: NCT04612608 Completed - ARDS, Human Clinical Trials

Assessing the Role of Inclined Positioning in Acute Respiratory Distress Syndrome Patients Recovery

ARISE
Start date: May 26, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of intermittent, nearly vertical, patient positioning in a specialized upright bed, on outcomes of mechanically ventilated patients with acute respiratory distress syndrome (ARDS) who are in the ICU.

NCT ID: NCT04612478 Completed - Clinical trials for Musculoskeletal Injury

Use of a Self-Directed Exercise Program (SDEP) Following Selected Lower Extremity Fractures

Start date: March 14, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effectiveness and value of clinic-based physical therapy (PT) and a home-based, self-directed exercise program (SDEP). The home exercise program will be developed by a team of physical therapists, orthopaedic trauma surgeons and experts in rehabilitation engagement in collaboration with patients recovering from traumatic lower-extremity injuries. The study will also determine which subgroups of individuals based on patient and injury characteristics are the best candidates for a home exercise program.

NCT ID: NCT04612400 Completed - Healthy Clinical Trials

Whole Body Protein Metabolism of a Whey/EAA Supplement Using Continuous Oral Stable Isotopes

Start date: November 4, 2020
Phase: N/A
Study type: Interventional

To evaluate the validity of a continuous oral sip-feeding method of stable isotope tracer for the evaluation of whole-body protein metabolism in response to two different doses of an EAA/whey protein supplement (Low=6.3g and High=12.6g). Results will be compared to those previously determined by constant infusion with the same EAA/whey supplement.

NCT ID: NCT04612374 Completed - Misophonia Clinical Trials

Exploring the Acceptability and Efficacy of a Transdiagnostic Treatment for Misophonia

Start date: December 21, 2020
Phase: N/A
Study type: Interventional

Despite increasing recognition of misophonia, there are currently no evidence-based treatments to help those who are suffering. Therefore, the primary purpose of this study is to assess the acceptability, feasibility, and preliminary efficacy of a treatment for misophonia. This study will be conducted in two phases. In the Phase 1, participants will receive a treatment the investigators believe can help manage symptoms of misophonia: The Unified Protocol. This treatment uses evidence-based psychological principles (e.g., managing attention or behavior) in a flexible manner and will focus on developing skills to help reduce the distress and impairment associated with Misophonia. After treatment, patients will provide feedback about their experience. The investigators will use this feedback to revise the treatment as indicated. In Phase 2, participants will receive the revised treatment and provide feedback on their experience. Throughout treatment in either phase, participants will provide daily and weekly information about their symptoms. The aims of this study are (1) to explore the acceptability and feasibility of the Unified Protocol for individuals who experience Misophonia and (2) to examine whether this treatment helps reduce symptoms associated with Misophonia.

NCT ID: NCT04612231 Completed - Clinical trials for Autism Spectrum Disorder

Examining the Efficacy of the T-STEP

Start date: December 11, 2020
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the TEACCH School Transition to Employment and Post-Secondary Education (T-STEP) Program. Through randomized assignment young adults (18-21 year-old) with ASD will participate in the full T-STEP Program or a counseling only condition. Effectiveness will be assessed by caregiver report (social communication, executive function, employment readiness), self-report (self-determination, coping, depression), and behavioral observation (i.e., a mock employment experience). The long-term impact of this intervention is to promote a more positive quality of life for young adults with high functioning ASD including increased postsecondary education completion, employment, self-determination, and decreased difficulties with coping and depression.

NCT ID: NCT04612114 Completed - Clinical trials for Obstructive Sleep Apnea

Pulse Oximeter for Sleep Evaluation

ROSA
Start date: July 21, 2020
Phase:
Study type: Observational

The investigators will conduct this study to validate Belun Ring for sleep assessment. The investigators will compare Belun Ring data collection and overnight in-lab polysomnography (PSG) measures of SDB and sleep architecture in adults with OSA symptoms. The investigators propose to recruit a total of 40 participants with symptoms of obstructive sleep apnea. The investigators will i) validate the overall accuracy, sensitivity and specificity of Belun Ring to assess SDB and sleep architecture, using PSG analysis as a gold standard.