Clinical Trials Logo

Filter by:
NCT ID: NCT06090552 Not yet recruiting - Clinical trials for Surgical Advanced Care Planning

I CAN DO Surgical ACP

Start date: June 2024
Phase: N/A
Study type: Interventional

The goal of the Advanced Care Planning (ACP) study is to encourage patients aged 65 or older, or with serious illness, who are referred for major elective surgery to have advanced care planning. ACP is also a critical way to support older adults in participating actively with clinicians in making real-time, complex medical decisions so that the medical care they receive is aligned with their goals. Our team has designed and tested a theory-based, interactive ACP patient-facing technology solution (PREPARE) based on the new ACP paradigm of preparing people for communication and medical decision-making. The study team hypothesizes that by including PREPARE into the electronic health record (HER)-centric pre-surgery workflow for older adults and including automated reminders, the study team can empower patients and surgical teams to engage in ACP discussions. Participants will be randomized to Arms: (1) Letter about ACP, PREPARE advanced directive (AD), PREPARE website; (2) Letter, advanced directive (AD), PREPARE plus reminder text/phone messages; (3) Letter, advanced directive (AD,) PREPARE plus reminders plus a healthcare navigator on ACP documentation (discussions and careplans, primary outcome) and patient-reported ACP engagement. Using mixed methods, the study team will assess patients' and surgical care teams' experience with surgery ACP.

NCT ID: NCT06090513 Not yet recruiting - Advanced Cancer Clinical Trials

Molecular Services and EMR-Lab Integration Application (ELIA) for Reducing Healthcare Disparities in Cancer Patients

Start date: October 18, 2023
Phase:
Study type: Observational

The goal of this observational study is to measure and try to reduce leakage in precision medicine care in the community cancer clinic. The goal of precision medicine is to identify the best possible therapy the the patient based on the biology of the tumor. Leakage is defined as a failure or inefficiency of the system that leads to dropped or lost testing, reporting or action (including drug selection). It has been observed that there are healthcare disparities in the community setting compared to academic medical centers, particularly in the use of precision medicine. The main questions the study aims to answer are: - How much leakage occurs in the use of precision medicine in the community setting? - Can we reduce leakage by providing access to better tools and services typically found in the academic medical centers? Participants will not be directly impacted and will receive standard of care. Measurements will be made of how often physicians select the appropriate test for patients, and how often they select the most appropriate therapy for their patients before and after the implementation of tools created to reduce leakage. We hope to reduce leakage in with the use of advanced tools and services, and use this study as a model to improve healthcare in the community cancer setting.

NCT ID: NCT06090279 Not yet recruiting - Thoracic Trauma Clinical Trials

Feasibility of the Gamification of Incentive Spirometry in Trauma Patients

Start date: January 2025
Phase: N/A
Study type: Interventional

Gamification may be one solution that can increase the compliance in the use of devices like incentive spirometry.

NCT ID: NCT06090097 Not yet recruiting - Knee Osteoarthritis Clinical Trials

Knee Biofeedback Rehabilitation Through Game Therapy

KneeBRIGHT
Start date: January 2024
Phase: N/A
Study type: Interventional

The goal of this study is to learn about the effect of video-game based rehabilitation exercise for patients with knee osteoarthritis. The main question the study aims to answer is: do patients who exercise with the game have better functional outcomes and engagement compared to patients who do conventional exercise? Participants will complete 10 weeks of physical therapy exercise sessions that focus on quadriceps strengthening. Two sessions per week will be conducted in the clinic, and one session will be conducted at home each week. The interventional group will conduct all exercises using the KneeBRIGHT EMG sensors and game software. The control group will conduct all exercises following a standard physical therapy regimen. Researchers will compare knee function and engagement between the group who uses the game, and the group who does conventional exercise.

NCT ID: NCT06090071 Not yet recruiting - Photoaging Clinical Trials

Trial Evaluating Both Tolerability and Improvement for Signs of Facial Photoaging, Discoloration, and Texture in Adult Females of All Skin Types by Combining a Placebo Moisturizer and Non-ablative Laser.

Start date: December 2023
Phase: Phase 4
Study type: Interventional

This is a phase 4 trial evaluating the clinical effect of combining a placebo moisturizer and non-ablative laser to improve procedural outcomes in patients with facial dyschromia. This study's objective is to evaluate both the tolerability and improvement in signs of photoaging for a placebo moisturizer used in combination with a non-ablative laser. Physician assessments, patient reported outcomes, and digital photos will be captured.

NCT ID: NCT06089746 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Lumbosacral Spinal Stenosis - Non-Invasive Postural Therapy for Older Adult Veterans

LSS-NIPT
Start date: February 15, 2024
Phase: N/A
Study type: Interventional

Lumbosacral spinal stenosis (LSS) is a leading cause of limited mobility, reduced independence, and poor health outcomes in older adults, and is very common in older adult Veterans. Several years ago, major research studies indicated that surgery for LSS was more effective than usual (medical) management. Nonetheless, there are many patients for whom surgery is not the ideal therapy. There have been reports that modifications in daily activities including temporary use of a modified rolling walker and changes in sleep positioning may help relieve LSS. The investigators have assembled a VA team to study this carefully. The investigators will recruit a small group of older adult Veterans with LSS to try out this program; the investigators will monitor them closely for relief of their symptoms and improvements in walking. The investigators will, as part of this small study, try to understand potential barriers to use of this therapy. The investigators will interview the Veterans and healthcare providers to identify problems that may arise in trying this therapy. If this small study works, the investigators plan to expand the effort.

NCT ID: NCT06089499 Not yet recruiting - COPD Clinical Trials

Palliative Care Health Literacy Education and QOL Compared to Usual Care

PACED
Start date: November 1, 2023
Phase: N/A
Study type: Interventional

The goal of this pilot randomized controlled trial is to compare health literacy (HL) and quality of life (QOL) among older adults with chronic obstructive pulmonary disease (COPD) who completed a series of standardized palliative care (PC) educational video learning modules to usual care (US). The main question[s] it aims to answer are: Between Groups: - What effect does completing a series of standardized PC education video learning modules have on HL among older adults with COPD treated in the emergency department (ED) compared to usual care? - What effect does completing a series of standardized PC education video learning modules have on QOL among older adults with COPD treated in the ED compared to usual care? Within Groups: - What is the change from baseline to study completion for older adults with COPD who receive the educational intervention series of PC learning modules on HL? - What is the change from baseline to study completion for older adults with COPD who receive the educational intervention series of PC learning modules on QOL? - What is the change from baseline to study completion for older adults with COPD who receive UC on HL? - What is the change from baseline to study completion for older adults with COPD who receive UC on QOL? All participants will complete a baseline and study completion health literacy questionnaire (HLQ) and Medical Outcomes Study: Short Form 36 survey. The treatment group will view one standardized learning module per week for four weeks provided by Get Palliative Care and log their weekly completion in REDCap. The control group will receive usual COPD care. Researchers will compare the treatment group receiving weekly palliative care education to usual care to see if HL and QOL change.

NCT ID: NCT06089135 Not yet recruiting - Clinical trials for Treatment in Calcified Coronary Disease

Shockwave Lithoplasty Compared to Cutting Balloon Treatment in Calcified Coronary Disease - A Randomized Controlled Trial

Short-Cut
Start date: December 31, 2023
Phase: Phase 4
Study type: Interventional

The Short-Cut trial is a prospective, investigator-initiated, multicenter, randomized controlled trial that is designed to compare the efficacy of cutting balloon angioplasty vs. intravascular lithotripsy prior to drug-eluting stent implantation in patients with moderate to severely calcified coronary arteries.

NCT ID: NCT06089057 Not yet recruiting - Clinical trials for Lower Extremity Muscle Strength

Pro-social Power Training Activity for Aging and Well-being With Chronic Kidney Disease

Start date: July 1, 2025
Phase: N/A
Study type: Interventional

This is a pilot trial of a 16-week physical activity and power training program among 30 Veterans/arm with advanced chronic kidney disease. The trial aims to test whether the program is tolerable to Veterans.

NCT ID: NCT06088355 Not yet recruiting - Parkinson Disease Clinical Trials

Moderate Versus High Volume Light-Moderate Intensity Exercise for People With Moderate Parkinson's Disease

HI-LITE
Start date: June 1, 2024
Phase: N/A
Study type: Interventional

Veterans with mid to later stage Parkinson's disease (PD) may not be able to work out as hard as they need to, to prevent brain cell loss. Maybe they could work out longer and more frequently to make up for this during their good times and good weeks and then rest during the bad weeks. The investigators will compare how effective working out a lot one week per month with a break of three weeks is to continuously exercising weekly with no breaks in people with mid stage PD. The investigators will look at how fast participants walk per minute, whether they become more physically active, the biochemicals in their blood, and at how stiff their blood vessels are before and after the exercise.