Clinical Trials Logo

Filter by:
NCT ID: NCT05419219 Enrolling by invitation - Fatigue Clinical Trials

TaiChi-DTx for Treating Long Covid Symptoms

TaiChi-DTx
Start date: June 1, 2022
Phase: N/A
Study type: Interventional

The randomized controlled trial will be conducted to evaluate the effectiveness of a Multi-domain Tai Chi Digital Therapy for treating the individuals suffering from the long term COVID-19 syndrome (Long COVID).

NCT ID: NCT05417685 Enrolling by invitation - Clinical trials for Musculoskeletal Diseases

Digital Care Programs for Musculoskeletal Health

Start date: July 26, 2022
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to create a research repository, composed of data collected in the course of digital care programs for musculoskeletal conditions and musculoskeletal health delivered by SWORD Health to individuals undergoing those programs. This will allow the investigators to observe the acceptance, engagement and outcomes of programs using this approach in the treatment of multiple musculoskeletal disorders (MSD).

NCT ID: NCT05416281 Enrolling by invitation - Clinical trials for Environmental Exposure

Customized Approaches for Evaluating and Reducing Chemical Exposures From Home Building Materials

Start date: August 11, 2022
Phase: N/A
Study type: Interventional

This project will evaluate new approaches to quantify and reduce chemical exposures from common building materials, with an emphasis on plastic additives, pesticides, flame retardants and lead in addition to other environmental contaminants. The objective of this project is to develop methods to quantify and reduce chemical exposures from the home environment using approaches that are adaptable and customizable to individuals and households. To achieve this goal investigators will: 1) Identify the types of building materials and housing characteristics associated with higher levels of exposure to different classes of contaminants; 2) Assess the effectiveness of a simple robotic vacuuming intervention for reducing exposure to a range of indoor contaminants; and 3) Evaluate a new wearable silicone wristband for monitoring exposure to lead and other metals.

NCT ID: NCT05415800 Enrolling by invitation - Cancer Clinical Trials

Quality Improvement Pilot

Start date: April 29, 2022
Phase: N/A
Study type: Interventional

The overall goal of this study is to develop and pilot test the use of practice facilitation as an intervention for healthcare providers and staff, with the goal of improving the implementation of cancer prevention and screening guidelines in primary care settings.

NCT ID: NCT05415371 Enrolling by invitation - Pregnancy Clinical Trials

Persistent Poverty Counties Pregnant Women With Medicaid

Start date: September 30, 2022
Phase: N/A
Study type: Interventional

Although many women initially quit smoking during pregnancy, most will return to smoking by the end of pregnancy or during the first 6 months postpartum. The proposed pilot project is designed to evaluate the feasibility and potential efficacy of offering small financial incentives for the completion of smoking cessation coaching and biochemically-verified smoking abstinence at follow-up among pregnant women with Medicaid insurance who contact the Oklahoma Tobacco Helpline (OTH). The study will enroll 100 pregnant women who will be randomly assigned to OTH care or OTH plus escalating incentives (OTH+I) for completing up to 5 coaching calls over the first 8 weeks after enrolling (prepartum) and for biochemically-verified smoking abstinence at 9 weeks post-enrollment (assessed remotely via smartphone). In addition, participants will be incentivized for completing a postpartum coaching call by 8 weeks postpartum. Feasibility outcomes for the incentives based intervention will focus on coaching call completion, rates of prepartum and postpartum follow-up, biochemically-verified smoking cessation, and perceptions of the intervention. Potential effectiveness will be evaluated by comparing biochemically-verified smoking abstinence rates in OTH+I relative to OTH alone at 12 weeks post-enrollment (prepartum) and 12 weeks postpartum.

NCT ID: NCT05414955 Enrolling by invitation - IBD Clinical Trials

Boom-IBD Clinical Trial

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

Feasibility study of neuromodulation in patients with IBD.

NCT ID: NCT05413070 Enrolling by invitation - Back Pain Clinical Trials

Quality Improvement re: Choosing Wisely Back Pain Measures

SCV LBP
Start date: June 15, 2022
Phase:
Study type: Observational

As

NCT ID: NCT05412342 Enrolling by invitation - Opioid Use Clinical Trials

Characterizing the Association Between Preoperative Depressive Symptoms and Opioid Use/Misuse After Surgery

Start date: May 10, 2019
Phase:
Study type: Observational

This observational study aims to characterize the relationship between preoperative depressive symptoms and opioid use/ misuse after surgery using a perioperative learning health care system. We will follow a prospective cohort of patients undergoing elective surgery.

NCT ID: NCT05411393 Enrolling by invitation - Frailty Clinical Trials

Synergizing Home Health Rehabilitation Therapy

Start date: October 6, 2022
Phase: N/A
Study type: Interventional

The objective of this project is to pilot test an ADL (activities of daily living)-enhanced program as an adjuvant therapy to usual home health rehabilitation to improve patient outcomes. The project will compare the ADL-enhanced program plus usual care with usual care using an RCT design in home health patients.

NCT ID: NCT05408520 Enrolling by invitation - Amputation Clinical Trials

Targeted Muscle Reinnervation Study (TMR)

TMR
Start date: May 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effect of targeted muscle reinnervation on the outcomes of amputees at a level 1 trauma center. The investigators propose to randomize all patients requiring amputation with and without targeted muscle reinnervation. This study will help delineate the efficacy of targeted muscle reinnervation in the general population.