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NCT ID: NCT06444724 Recruiting - Colonoscopy Clinical Trials

The Effect of Smartphone Application on the Quality of Bowel Preparation for Colonoscopy

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

The goal of this clinical trial is to learn about bowel preparation methods compared between standard techniques and enhanced education with application for elective colonoscopy. The main questions it aims to answer are: Which bowel preparation method results in an adequate bowel preparation rate? Participants will: - Random to 1:1 ratio to be educated via the smartphone application (APP group) or the standard education (control group). - Received the same purgative regimen and diet restriction. - Endoscopist-blinded colonoscopy the participants and give score of bowel preparation scale (use Boston Bowel Preparation Scale)

NCT ID: NCT05700435 Recruiting - Anxiety Clinical Trials

Resiliency in U.S. Air Force Personnel

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

The goal of this clinical trial is to examine the effectiveness of the Stress Management and Resilience Training (SMART) in increasing resilience in a population of U.S. Air Force personnel at Joint Base Andrews, Joint Base San Antonio-Lackland, Nellis Air Force Base, and Wright-Patterson Air Force Base. The main questions it aims to answer are: 1. When delivered in real-world conditions, to what extent does SMART increase levels of resiliency and decrease levels of stress in a sample of active component U.S. Air Force personnel? 2. Does SMART have a sustained effectiveness from baseline to 12, 24 and 36-weeks after training completion in a sample of active component U.S. Air Force personnel? 3. Does SMART provided via an in-person/video-teleconference (VTC) or Computer-Based Training (CBT) modality demonstrate equivalent effectiveness in increasing resilience and decreasing stress in active component Air Force personnel? Participants will be asked to complete a pre-intervention survey, complete the assigned modality of SMART ( in-person/VTC or CBT), and complete follow-up measurements at 12-, 24-, and 36-weeks post-intervention completion. Researchers will compare in-person/VTC and CBT groups' measurements to see if a difference in self-reported resilience, stress, anxiety, or quality of life is present pre-intervention. Researchers will compare in-person/VTC and CBT groups' measurements to see if a difference in self-reported resilience, stress, anxiety, or quality of life is present post-intervention.

NCT ID: NCT05132868 Recruiting - Quality Clinical Trials

Assessments of Genetic Counseling Augmented With an Educational Video or Pamphlet Versus Traditional Counseling

Start date: August 25, 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to understand the impact of an educational video or pamphlet on the patient experience in a hereditary cancer genetic counseling program. In order to make this assessment, it is necessary to perform qualitative and quantitative research among patients in a hereditary cancer genetic counseling clinic.

NCT ID: NCT04676347 Recruiting - Evaluation Clinical Trials

Health-care Quality in Semi-intensive Care Units

Start date: July 1, 2021
Phase:
Study type: Observational

The main aim of this study is to realize a system of continuous evaluation of healthcare quality in semi-intensive care units.

NCT ID: NCT04039997 Completed - Resuscitation Clinical Trials

How to Learn Cardiopulmonary Resuscitation

Start date: July 20, 2019
Phase: N/A
Study type: Interventional

the aim of the study is to evaluate two methods of teaching cardiopulmonary resuscitation in the context of chest compression quality. We will evaluate the usefulness of the application cpr feedback device (CPRMeter) for quality of chest compression.

NCT ID: NCT02274441 Completed - Gynecology Clinical Trials

Activity and Quality of Care Indicators' for a Sentinel Network Creation

URGO
Start date: January 2015
Phase: N/A
Study type: Observational

There is no large-scale data in France or internationally, on the quality of care in gynecological emergencies, or the consequences of delay or misdiagnosis of women's health or on determinants of these delays or misdiagnosis. The creation of a sentinel network for gynecological emergencies could help quantify these links and test strategies to avoid the worst effects by implementing simple diagnostic tools from clinical research. The network will be designed to promote research in women's health and the emergency reception by focusing on: (i) Assessment of the quality and organization of care and professional practice for the management of gynecological emergencies. (ii) The study of severe morbidity and its determinants (iii) comparison of organizational practices and health outcomes of women over time within the same department or between services having substantially the same recruitment (iv) Comparison of organization systems gynecological emergencies departement between different high resource francophone countries (France, Switzerland, Belgium). (v) The assessment of new diagnostic strategies (sorting or diagnostic aid) or therapeutic derived from clinical research.

NCT ID: NCT01069107 Completed - Morbidity Clinical Trials

Acute Admission to Hallingdal Sjukestugu

Start date: April 2010
Phase: N/A
Study type: Interventional

The main objective of the project is to assess whether a community hospital may have or should have a role in the Norwegian health care system in the acute treatment of a defined group of patients.