Clinical Trials Logo

Filter by:
NCT ID: NCT05704764 Enrolling by invitation - HIV Clinical Trials

Using the Ending Self-Stigma Intervention to Reduce Internalized Stigma Among People Living With HIV Who Use Substances

IRIS
Start date: February 17, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to test an intervention to reduce stigma among people living with HIV who use opioids and cocaine. The main question it aims to answer is: - Does reducing internalized stigma about HIV and/or drug use lead to improved HIV care outcomes? After a year spent adapting an existing intervention to be applied specifically among people living with HIV who use substances, 70 participants will be randomized to receive either treatment-as-usual or the newly adapted intervention. The intervention itself will consist of less than ten group-based meetings to discuss and work through the stigmas people commonly associate with HIV and/or drug use.

NCT ID: NCT05704309 Enrolling by invitation - Diabetes Clinical Trials

The Diabetes Prevention Program Outcomes Study AD/ADRD Project

DPPOS-4
Start date: November 7, 2022
Phase:
Study type: Observational

The DPPOS AD/ADRD project will address the overarching question: What are the determinants and the nature of cognitive impairment among persons with pre-diabetes (PreD) and type 2 diabetes (T2D), who are a high-risk group for cognitive impairment and represent a large fraction of the United States (US) population? This U19 proposal addresses the National Alzheimer's Project Act goal to "prevent, halt, or reverse AD" in the high-risk group of persons with pre-diabetes and type 2 diabetes, who represent over half of the population aged 60 years and older in the US.

NCT ID: NCT05703412 Enrolling by invitation - Schizophrenia Clinical Trials

Effectiveness of mHealth Post-discharge Intervention for Patients With Severe Mental Illness

tFOCUS
Start date: February 14, 2023
Phase: N/A
Study type: Interventional

The overall aim of this program of research is to improve the continuity of care for patients with serious mental illness (SMI) by supporting a safer and more efficient bridge from hospital to outpatient care using a mobile device-delivered app called Transition-FOCUS (tFOCUS), which has previously been tested in community samples. The purpose of the proposed project is to establish the effectiveness of our empirically-supported, multi-component mHealth intervention.

NCT ID: NCT05702515 Enrolling by invitation - Peripheral ICC Clinical Trials

Vascular Positioning System G4 Algorithm ECG Data Collection for Model Training Study

Start date: July 21, 2023
Phase:
Study type: Observational

The objective of this study is to collect intravascular and extravascular echocardiogram (ECG) data from subjects receiving peripherally inserted central catheters (PICC) while using the Vascular Positioning System G4 and a 12 lead ECG machine. The data obtained will be used to update the G4 algorithm.

NCT ID: NCT05700370 Enrolling by invitation - Prostate Cancer Clinical Trials

MyProstateScore Equivalency With and Without DRE

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to quantify the concordance of MPS results between first-catch urine samples collected post-DRE and those collected without a DRE.

NCT ID: NCT05699343 Enrolling by invitation - Surgery Clinical Trials

Surgical Treatment of Peri-implantitis Using a Bone Substitute With or Without a Resorbable Collagen Membrane

Start date: January 30, 2023
Phase: N/A
Study type: Interventional

The objective of the present randomized clinical trial will be to compare two surgical methods of treating peri-implantitis. This study will determine if surgical debridement of peri-implantitis bone defects, including air decontamination of implant surfaces, in combination with the placement of a bone graft, differs in treatment outcomes compared to placing the same bone graft material with a resorbable collagen membrane placed over the bone graft.

NCT ID: NCT05696899 Enrolling by invitation - Pain Clinical Trials

Determining the Efficacy of Essential Oil Aromatherapy in Children Undergoing Port Access

Start date: December 5, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of aromatherapy impacts patient anxiety and pain scores surrounding port access in pediatric oncology patients between the ages of 4 years and 18 years.

NCT ID: NCT05694832 Enrolling by invitation - Clinical trials for Graft Versus Host Disease

Expressive Writing in GVHD

EXPRESS-C-GVHD
Start date: January 21, 2023
Phase: Early Phase 1
Study type: Interventional

Graft-versus-host-disease (GVHD) is a disease phenomenon that occurs when immune cells of the donor recognize and attack healthy tissue within the transplant recipient, or host. It is ultimately the result of the same immunological mechanisms that provide benefit to patients receiving hematopoietic stem cell transplantation (HSCT). In patients with hematologic malignancies, HSCT can be therapeutic, as donor T cells recognize and mount a response against cancerous cells. HSCT is also used in the setting of certain immunodeficiencies and inborn errors of metabolism for which therapeutic benefit is found in immunologic repletion. To our knowledge, support groups have yet to be investigated in academic literature as a nonpharmacologic, therapeutic intervention for cutaneous GVHD patients to improve their distress, systemic disease, and quality of life. Given the dearth of research on nonpharmacologic therapies for cutaneous GVHD that address quality of life impairments, we seek to characterize the effect of an expressive writing and peer helping intervention contextualized within the framework of a support group. The primary goal of this study is to provide preliminary efficacy data of expressive writing as an intervention in patients with cutaneous GVHD to trial.

NCT ID: NCT05692440 Enrolling by invitation - Low Back Pain Clinical Trials

Basivertebral Nerve Ablation With the Intracept Procedure

Start date: May 3, 2021
Phase: Phase 4
Study type: Interventional

This is an independent prospective, noninterventional, single arm post market data collection of the patient-reported effectiveness, ongoing safety, and satisfaction outcomes for patients treated with intraosseous basivertebral nerve ablation using the Intracept Procedure at a single study site.

NCT ID: NCT05692401 Enrolling by invitation - Body Weight Changes Clinical Trials

Weight Change With Controlled Ankle Movement (CAM) Boot Use

CAM
Start date: June 7, 2023
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if patients wearing a CAM boot have a change in weight compared to patients who wear a CAM boot and are provided nutritional guidelines and perform upper body exercises.