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Knowledge, Attitudes, Practice clinical trials

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NCT ID: NCT05580939 Completed - Satisfaction Clinical Trials

The Effect of a Web-based Simulation Application

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

Cardiopulmonary resuscitation (CPR) training for nursing students is important. The importance of using computer-assisted simulation in gaining skills for basic life support applications is increasing. In addition to the use of simulation-based teaching methods in many different fields, it is seen that they are also used for the development of cardiopulmonary resuscitation practices of students and produce effective results.The aim of the study is to evaluate the effect of a web-based simulation application used in basic life support education on the level of knowledge, satisfaction and self-confidence of nursing students.

NCT ID: NCT05567900 Completed - Clinical trials for Urinary Incontinence

Health Care Seeking Behavior and Knowledge Assessment of Hungarian Women About Pelvic Floor Disorders

Start date: March 4, 2022
Phase:
Study type: Observational

The aim of this study is to assess women's health care seeking behavior and knowledge of urinary incontinence and pelvic organ prolapse and to culturally adapt the Prolapse and Incontinence Knowledge Questionnaire (PIKQ) for the Hungarian population.

NCT ID: NCT05564507 Completed - Clinical trials for Cardiovascular Diseases

Effectiveness of Simulation-based Training on Transoesophageal Echocardiography Learning

SIMULATOR
Start date: November 1, 2020
Phase: N/A
Study type: Interventional

Background: Simulation-based training in transesophageal echocardiography (TEE) seems promising. However, data are limited to non-randomized or single-center studies. Objectives: This large multicenter randomized, parallel-group, unblinded, study will assess the impact of simulation-based versus traditional teaching on TEE knowledge and performance for medical fellows in cardiology. Eligibility: - All consecutive fellows in cardiology of all training levels (year 1-4) - who have never performed a TEE alone Design: - Multicenter, parallel-group, unblinded, randomized study with a prospective enrollment of all consecutive fellows in cardiology of all training level (year 1 to 4) who were recruited in 42 centers throughout France. - Randomization with stratification by center will be performed at the individual (fellow) level in 1:1 ratio to assign all the fellows to the traditional group or to the TEE simulation-based training group. - Each participant will complete two different tests during the study: 1) a pre-training test before starting the educational program; and 2) a final test performed 3 months after the end of the educational program. Each of these tests will include a theoretical test and a practical test on a TEE simulator. - The coprimary outcomes of the study to compare the two groups will be the scores in the final theoretical and practical tests after the training will be completed.

NCT ID: NCT05514808 Completed - Clinical trials for Knowledge, Attitudes, Practice

An Intervention to Improve Knowledge on Dietary Supplements Among Varsity Athletes

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

The aim of this project is to increase knowledge on and influence intention (and related determinants) toward the use of dietary supplements in populations at risk for doping such as university student athletes. Our objectives are to increase athletes' knowledge on dietary supplements, change their attitude, subjective norms and perceived behavioural control toward the use of these supplements, increase their body appreciation and thus increase their intention to take nutrients from diet first before considering dietary supplements. We are proposing the conceptualization, implementation, and evaluation of a nutrition education program on dietary supplements targeting varsity athletes at universities across Ontario. Participants will be recruited from varsity teams at the University of Guelph. The intervention will be tested for validity and reliability and implemented online through Courselink modules over 4 weeks. Participants will be randomly assigned to a control or intervention group, using a randomized control trial approach. Each week, participants will learn about a topic related to nutrition, health and values-based ethics of clean sport. The intervention group will receive additional information on dietary supplements, their benefits and their risks. Doping and body appreciation and their links to the use of dietary supplements will also be covered in this group. A questionnaire assessing outcome objectives will be administered before and at the end of the intervention as well as 3 months post-intervention. Among the different components covered in the questionnaire, one section will assess knowledge on health, sports nutrition, and dietary supplements; and another will gather responses to statements reflecting the different theory of planned behaviour (TPB) cognitive constructs.

NCT ID: NCT05422872 Completed - Clinical trials for Knowledge, Attitudes, Practice

Delphi Study on Psychological Safety Competencies in Healthcare Training Curricula

Start date: January 25, 2022
Phase:
Study type: Observational

Psychological safety refers to the shared belief that a work team can face complex challenges when there is an environment of mutual respect and trust. Thus, healthcare professionals provide safer care when causes and ways to avoid clinical errors can be discussed and analyzed without fear of criticism or sanctions. A psychological safety climate can be a determinant of patient safety. In this way, this provides safer care when it is possible to discuss and analyze the causes and how to avoid clinical errors without fear of criticism or sanctions. This study aims to explore the mentors' opinion on what psychological safety competencies are being acquired by future generations of healthcare professionals (students and residents, hereafter "trainees") through current training programs and what actions should be taken to promote such competencies in clinical settings.

NCT ID: NCT05421637 Completed - Clinical trials for Knowledge, Attitudes, Practice

Knowledge and Perception of Evidence-based Psychology in Latin American Psychologists

Start date: November 15, 2020
Phase:
Study type: Observational

This was a non-experimental, descriptive, prospective and cross-sectional study, for which the CHERRIES checklist was used to report the study in order to improve the quality of the report of such designs. The open-ended survey was voluntary, consisted of 18 items and four sections, the items were not randomized and the survey was estimated to last approximately five minutes.

NCT ID: NCT05297721 Completed - Nurse's Role Clinical Trials

Nurses' Level of Knowledge on Skin Tears: A Cross-Sectional Study

Start date: September 1, 2021
Phase:
Study type: Observational [Patient Registry]

Skin tears (ST) are one of the skin integrity problems encountered in healthcare settings with rates equal to or greater than pressure injuries. However, the importance of this problem has been emphasized in the literature in recent years. This study was conducted to determine the knowledge level of nurses about ST.

NCT ID: NCT05284669 Completed - Low Back Pain Clinical Trials

Effect of an E-learning Intervention on Knowledge, Attitudes and Beliefs of Healthcare Professionals Managing Low Back Pain.

Start date: August 27, 2021
Phase: N/A
Study type: Interventional

The purpose of the current research project is to examine if the healthcare professionals (HCPs) knowledge, attitudes, beliefs and behavior about the management of low back pain (LBP) patients changes following an e-learning intervention (experimental interactive e-learning versus traditional non-interactive e-learning)

NCT ID: NCT05248542 Completed - Virtual Reality Clinical Trials

The Effects of Virtual Reality/ Augmented Reality Usage on Oral Care Knowledge in Nursing Students

Start date: March 23, 2021
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the effects of virtual reality usage on oral care knowledge in nursing students. The participants were randomly assigned to virtual-reality experimental and control groups. The students in experimental group received a 30 minutes virtual reality (VR) training for elderly oral health care at the second week and the fourth week after the first time survey. All students self-administrated questionnaire three times at first date of consent form signed, immediately after each of the intervention for period of two weeks. Linear regression in generalized estimating equations (GEE) compare the differences between both groups.

NCT ID: NCT05244161 Completed - Child Development Clinical Trials

A Quasi-experimental Evaluation of the Malezi Program in Tanzania

Malezi II
Start date: October 13, 2019
Phase: N/A
Study type: Interventional

The quality of caregiving and the parent-child relationship is critical for early child development (ECD) and has been shown to be modifiable. This study evaluated an ECD project in Tanzania, assessing the effectiveness of radio messaging (RM) alone and a combined radio messaging/video job aids/ECD (RMV-ECD) intervention, using a two-arm pre-post design study, which enrolled a cohort of caregivers of children 0-24 months in four districts of Tabora region, following them for nine months. ECD radio messages were broadcast on popular stations at least 10 times/day reaching all study districts. In two districts, community health workers (CHW) trained in UNICEF's Care for Child Development package and used ECD videos in home- and facility-based sessions with caregivers. Five outcomes were used to assess the intervention effects: ECD knowledge, early stimulation, father engagement, responsive care, and environment safety. Additionally the effect of the training and video job aids on the quality of CHWs' counseling support was evaluated primarily using structured observation checklists of household visits and facility group counseling sessions with caregivers and their children. Qualitative data was collected from a subset of caregivers and CHW participating in the study to assess acceptability and other perceptions of the project.