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Patient Satisfaction clinical trials

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NCT ID: NCT05607238 Withdrawn - Clinical trials for Patient Satisfaction

Patient Perspective Midline Catheter in the Emergency Department

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

This study examines the patient satisfaction and perspective on the use of ultrasound guided midline intravenous catheters compared to standard ultrasound guided peripheral catheters.

NCT ID: NCT05350488 Withdrawn - Stroke Clinical Trials

Qualitative Analysis of the Post-Stroke Continuum Among African Stroke Survivors in Alabama

Start date: February 1, 2023
Phase:
Study type: Observational [Patient Registry]

This proposal seeks to improve the investigators' post-stroke TOC process through developing an innovative, patient informed and guided solution aimed at addressing the investigators' deep south African American population within the UAB system. The investigators will engage participants in both urban and rural Alabama through informational interviews and work to find common themes to address so that future interventions are useful to their unique needs and desires. This goes beyond simply identifying barriers and endeavors to discovering solutions.

NCT ID: NCT05182320 Withdrawn - Clinical trials for Patient Satisfaction

Study Measuring the Effects of Patient Data for Total Hip and Total Knee Arthroplasty Patients Using an APP Based Sensor for Home Exercise Performance Before and After Operation

ORTHOPATH
Start date: June 1, 2023
Phase:
Study type: Observational

Multicenter, Prospective, Randomized, Comparative Study Measuring the Effects on Clinical Outcomes, Patient Satisfaction, Costs and Benefits of Combined Pre-, Intra- and Postoperative Patient Data for THA and TKA Patients Using an APP Based Sensor for Home Exercise Performance Before and After Operation

NCT ID: NCT04647084 Withdrawn - Pain, Acute Clinical Trials

Pilot Trial: Comparing Buzzy to Intradermal Lidocaine for Peripheral IV Cannulation in Adults

Start date: October 15, 2022
Phase: Phase 4
Study type: Interventional

IV placement is necessary for surgical procedures. Unfortunately, some patients say that placing an IV is painful. The investigators are conducting this study to evaluate two techniques that could make the placement of the IV more comfortable.

NCT ID: NCT03934918 Withdrawn - Clinical trials for Patient Satisfaction

Outpatient Cervical Preparation to Reduce Induction Duration in NTSV Women

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

This study is to compare 2 groups in nulliparous women undergoing cervical ripening for induction of labor. The study hypothesis is that outpatient cervical preparation with a foley catheter can reduce the induction of labor (IOL) time interval from admission to delivery by 50%. A 30 ml transcervical foley catheter is a safe mode of cervical preparation in the outpatient setting, as concluded in Diederen et al, Sciscinoe et al, and Kelly et al. Findings from studies on nulliparous, term, singleton vertex (NTSV) showed patients can be applied to a wide variety of maternity unit sizes as discussed by Main et al. No previous study has evaluated the effectiveness of outpatient cervical preparation in the NTSV population by PUBMED search. Further, no previous study has assessed patient satisfaction cervical preparation in the outpatient setting and no previous study has evaluated whether outpatient cervical preparation has an impact on the length of stay and cost of hospitalization. This study will explore these important questions with the goal of improving current practices in labor induction to be more patient-centered, pragmatic, and cost-effective.

NCT ID: NCT03197311 Withdrawn - Post Operative Pain Clinical Trials

A Mobile Application for Post-op Analgesic Consumption

Start date: October 2019
Phase: N/A
Study type: Interventional

Surgical extraction of third molars is one of the most common outpatient procedures performed by oral surgeons. The prescription of postoperative narcotic and NSAID analgesics is the standard of care practice to relieve symptoms of pain, swelling, and trismus after these procedures. The majority of these patients do not return for follow up unless they experience a problem. There is limited data on whether the patients use the narcotics as directed and what is their practice of disposal of the remaining medications that were not consumed. In this research the effectiveness of postop analgesic consumption, analgesic disposal practice, pain control, and patient satisfaction will be compared between patients who are randomized to the intervention group who will use a developed mobile application and a control group who will not use the mobile app.

NCT ID: NCT03173794 Withdrawn - Clinical trials for Patient Satisfaction

CommunityRx for Hunger: A Hospital-Based Intervention

Start date: April 2018
Phase: N/A
Study type: Interventional

The goal of this research program is to reduce health disparities by deploying an information-based intervention to increase caregiver utilization of community-based food supports and satisfaction with care among food insecure caregivers of hospitalized children. We will conduct a randomized controlled trial to evaluate, versus usual care, the effects of the CommunityRx-H intervention on caregiver use of food resources (primary), caregiver patient satisfaction with care (primary), caregiver mental health-related quality of life (secondary), and caregiver household food security (secondary). The proposed research will yield an understanding of how to leverage a child's hospitalization to effectively intervene on the problem of food insecurity. Findings will inform the rapidly growing field of healthcare-based interventions to address health-related social needs.

NCT ID: NCT01350739 Withdrawn - Clinical trials for Patient Satisfaction

The Umbilical Access in Laparoscopic Surgery

Start date: May 2015
Phase: N/A
Study type: Interventional

The aim of this study is to access to the abdominal cavity using different incision-types within the umbilical area. Effects of different incisions on scarring and on the umbilical form will be investigated.