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NCT ID: NCT04560647 Completed - Psoriasis Clinical Trials

Pilot Studies Testing Levels of P63 in Psoriasis Skin Lesions

Start date: December 3, 2020
Phase:
Study type: Observational

The purpose of this study is to understand the role of a specific protein, tumor protein p63 in the skin disease psoriasis. This study is to further understand how psoriasis lesions happens. An understanding of key mediators that lead to psoriasis might aid in the discovery of more effective treatments for this skin disorder. This is not an intervention study. The study is looking to obtain currently untreated plaque psoriasis biopsies and also biopsies from non psoriasis patients. Psoriasis and medical history will be collected then skin biopsies will be obtained from the subjects.

NCT ID: NCT04560595 Completed - Anxiety Clinical Trials

Remote Guided Caffeine Reduction

Start date: September 10, 2020
Phase: N/A
Study type: Interventional

The purpose of this online research study is to determine whether or not a gradual caffeine reduction program developed at Johns Hopkins can help people reduce their caffeine use. The investigators will provide materials to help guide caffeine reduction and ask questions to track caffeine use over several weeks. The investigators will also assess how reducing caffeine may benefit common caffeine-related problems such as anxiety, sleep disturbances, and gastrointestinal distress. The study will also determine whether or not people like participating in this caffeine reduction program in an online format.

NCT ID: NCT04560556 Completed - Clinical trials for Human Immunodeficiency Virus

Linking Persons With HIV, Discharged From Jail, With Community Care

Start date: November 10, 2020
Phase:
Study type: Observational

This is a prospective cohort study of outcomes of individuals who entered jail during a period during which one of three serial HIV testing strategies is implemented. This study involves two sub-studies. One sub-study will examine referrals to HIV prevention programs for persons testing negative for HIV while in jail. The second sub-study will monitor antiviral use among those testing positive for HIV.

NCT ID: NCT04560478 Completed - White Spot Lesion Clinical Trials

Comparing Fluoride Varnish and Sealant to Prevent White Spots in Orthodontic Patients

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is o compare the efficacy of CPP-ACP MI Varnish and ProSeal sealant in preventing white spot lesion (WSL) formation in orthodontic patients.

NCT ID: NCT04560400 Completed - Concussion, Mild Clinical Trials

Reverse King-Devick Test and History of Multiple Concussions

Start date: September 20, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effects of concussion history and reading direction on baseline King- Devick Test (KDT) performance, a common component of sideline concussion assessments. The KDT is a timed assessment of saccades, or quick movements of the eyes between two points. This test is a form of rapid automatized naming and involved subjects reading digits arranged on a tablet screen as quickly and accurately as possible. The test has three progressively more challenging test "cards," as the horizontal guidelines between digits disappear from test card 1 to 2, and the vertical spacing between the lines of digits decreases from test card 2 to 3. KDT performance is evaluated in terms of both speed (duration to all three test cards) and the number of errors (digits read incorrectly or omitted). Previous studies have identified several factors that affect KDT performance aside from head injury, including age, sex, sleep deprivation, learning disabilities, and first languages other than English. History of concussion has not been shown to influence KDT performance. The investigators hypothesize that since the left-to-right (L-R) reading direction of the KDT is the same way in which to read English, the long-term effects of prior concussions on saccadic eye movements may be masked. The investigators want to answer the following three research questions: 1) What is the effect of KDT reading direction on baseline KDT performance? If the test is performed by reading digits in a right-to-left (R-L) direction, will KDT times be slower and the number of errors increase relative to a typical L-R KDT? 2) What is the effect of a history of multiple concussions on KDT performance relative to no history of concussion? 3) Is the R-L KDT more sensitive to a history of multiple concussions? The investigators hypothesize that individuals with a history of multiple concussions will perform significantly worse (longer test durations, more errors) than individuals with no concussion history on the R-L KDT. On the other hand, the investigators hypothesize that baseline performance on the traditional L-R KDT will not be able to discriminate individuals with a history of multiple concussions from those with no concussion history.

NCT ID: NCT04560088 Completed - Loneliness Clinical Trials

Mindfulness to Reduce Loneliness in Older Caregivers

Start date: January 5, 2021
Phase: N/A
Study type: Interventional

The objective of this pilot study is to provide initial evidence of the role of mindfulness training in improving social disconnectedness - including social isolation and feelings of loneliness - in older caregivers for family members with ADRD. The investigators propose a two-arm randomized control trial: participants will be randomized to (a) smartphone-based MBSR app (Headspace) or (b) active control (breathing app) for 14 days. Loneliness and quality of social interactions will be assessed using Ecological Momentary Assessment at baseline and 14-days after randomization.

NCT ID: NCT04560075 Completed - Depression Clinical Trials

Text 2 Connect- Texting Intervention for Mental Health Treatment Utilization

T2C
Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Text2Connect (T2C) proposes to test a text-based intervention designed to improve engagement with mental health treatment.

NCT ID: NCT04559854 Completed - Breast Cancer Clinical Trials

Mindful After Cancer: A Mindfulness-based Therapy Intervention for Sexual Health After Cancer

MAC
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The objectives of this study are to: 1) adapt a mindfulness-based therapy program designed to help women manage their sexual and body image concerns after cancer (Mindful After Cancer, MAC) to a videoconference format and 2) assess the feasibility, acceptability, and preliminary effects of the program among breast and gynecologic cancer survivors.

NCT ID: NCT04559802 Completed - Tooth Loss Clinical Trials

Submerged Versus Non-Submerged Healing of Implants Subjected To Contour Augmentation

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

It is a randomized controlled trial to evaluate two surgical techniques for dental implant placement simultaneously with bone augmentation.

NCT ID: NCT04559763 Completed - Hypoxia Clinical Trials

SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion Study

Start date: August 18, 2020
Phase:
Study type: Observational

SpO2 (oxygen saturation) and pulse rate accuracy of pulse oximetry equipment, OxySoft Sensor/N-600x and OxySoft Sensor/N-395, continuous measure of arterial oxygen saturation during hypoxic state throughout motion and non-motion conditions under one system configuration. The purpose of this Non-Randomized, Prospective,Observational study is to conduct a hypoxia study to directly compare a prototype OxySoft pulse oximeter system to arterial oxygen saturation.