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Hand Hygiene clinical trials

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NCT ID: NCT05872581 Completed - Hand Hygiene Clinical Trials

Education Program of Hand Hygiene for Nursing Students

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

The goal of this observational study is to design and test a multicomponent education program of hand hygiene in nursing students. The main aims are: 1. conduct a randomized controlled trial (RCT) to test the effectiveness of this program on knowledge and practice of hand hygiene in nursing students; 2. evaluate the effects of each component and collect feedbacks from participants. Participants will be randomly assigned into the three intervention: Group A (Hand scanner instant feedback) , Group B (Video training), Group C (Hand scanner + Video training) , and Group D (Control group without intervention). Pre- and post-intervention assessment will be used to evaluate the effectiveness of the program and individual components.

NCT ID: NCT05848596 Completed - Hand Hygiene Clinical Trials

Handwashing Knowledge and Practice of Palliative Care

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

This study was planned as a randomized controlled study to evaluate the effect of hand hygiene training given to the companions in the palliative care service with standard patient simulation on hand washing knowledge and practices. Companions who are over the age of eighteen, who are at least literate, who can communicate effectively, and who fully fill in the data collection tools will be included in the study. The key questions it aims to answer Does the hand hygiene training given with standard patient simulation have an effect on the hand washing knowledge of the attendants? Do the attendants participating in the hand hygiene training given with standard patient simulation have an effect on hand washing practices?

NCT ID: NCT04830761 Completed - Hand Hygiene Clinical Trials

Behavior Change in Context to Contain the Spread of COVID-19

Start date: March 26, 2021
Phase: N/A
Study type: Interventional

Project BECCCS (=Behavior Change in Context to Contain the Spread of COVID-19) aims to optimise and test a behaviour change intervention to promote correct hand hygiene at key times in the short and long term. The study's specific aims are: 1. Optimisation phase: Identify the most effective combination and sequence of three different intervention modules (habit, motivation, social norms), and to assess usability and fidelity measures in order to optimise the intervention 2. Evaluation phase: Test the final intervention against an active control group (basic app content including "Federal Office of Public Health" advice)

NCT ID: NCT04773288 Completed - Hand Hygiene Clinical Trials

Handy Hygiene of Children: Understanding the Effect of Live Feedback on Handwashing Behavior

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Objective of the randomized controlled trial is to assess the impact of a digital intervention on hand hygiene of young children. Children in intervention kindergartens / elementary schools will see live instructions and feedback on their current hand washing activity while washing hands. We hypothesize that the digital intervention will improve hand hygiene practices of children in kindergarten / elementary school.

NCT ID: NCT04654182 Completed - Hand Hygiene Clinical Trials

Evaluation of the Residual Antimicrobial Efficacy of One Test Material Based on a Modification of ASTM E1115-11 Test Method

Start date: November 30, 2020
Phase: Phase 4
Study type: Interventional

To evaluate the residual antimicrobial effectiveness of one test product when tested using a modification of the methodology of the standardized ASTM E115-11 (2017)

NCT ID: NCT04267952 Completed - Hand Hygiene Clinical Trials

Hand Hygiene Intervention Program on Primary School Students' Health Outcomes and Absenteeism in School

Start date: September 9, 2019
Phase: N/A
Study type: Interventional

The most common infections in schools are acute respiratory infections (colds, pharyngitis, influenza and others) and diarrheal diseases. The incidence of these infections may also be an important cause of school absenteeism, leading to negative outcomes in both education and health. WHO states that handwashing a well-known primary infection control measure, is the most important hygiene measure to prevent the spread of infection when handwashing is done with soap and water. Since behavioral choices that determine lifestyle are made in childhood, it is important that health education in hand hygiene be implemented as early as possible to improve healthy behaviors. In this context, schools are important structures for information and behavior change about water, sanitation and hygiene interventions. Planned Behavior Theory (PBT) states that intention is the main precursor of behavior. According to the theory, intention is guided by three independent variables (perceived behavior control, attitudes and subjective norms), and intention formation leads to the development of behavior. The theory has been used in a study to improve hand hygiene behavior in health workers, but it has not been used in the literature to improve hygiene behaviors in children. Researches indicate that students who do not attend school frequently or for a long time have difficulty in mastering the subject described in the lesson and that school absenteeism is an issue that should be emphasized in education. Therefore, hand hygiene has a simultaneous effect that improves both education and health and contributes to a safe and healthy learning environment. The aim of this research is; To test the effect of hand hygiene intervention program based on Planned Behavior Theory on students' health outcomes and school absenteeism.

NCT ID: NCT04102488 Completed - Hand Hygiene Clinical Trials

Simplifying the World Health Organization (WHO) Protocol for Hand Hygiene: Three Steps and 15 Seconds

SIHAG II
Start date: September 15, 2019
Phase: N/A
Study type: Interventional

This study is to investigate that non-inferiority in terms of reduction of bacterial counts will be retained when combining the simpler three-step technique for the use of hand rub with a shorter application time of 15 seconds.

NCT ID: NCT04053257 Completed - Neonatal Infection Clinical Trials

Effect of Video Camera Monitoring Feedback on Hand Hygiene Compliance and Infections in NICU

CaM-HAI
Start date: July 29, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if use of the video camera surveillance system for HH observation and performance feedback about HH compliance rates can improve the HH compliance of HCWs and reduce healthcare-associated infections in the NICU.

NCT ID: NCT04023682 Completed - Hand Hygiene Clinical Trials

ProvodineTM Decreases Hand Contamination

Start date: December 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see whether Provodine, an FDA approved product, provides long-lasting protection on the hands of staff who provide anesthesia for patients. If this product does provide long-lasting protection, it could be used for hand hygiene in the operating room and it could help prevent infections after operations. Fifteen anesthesia providers (15 main operating room [MOR] and 5 ambulatory surgery center [ASC]) who agree to participate will participate in the pre-intervention and intervention periods. During the pre-intervention or baseline period, the investigators will do bag broth cultures of anesthesia providers' hands just before the start of their first case of the day . The participants will then rinse and dry their hands to remove the culture medium. The investigators will also obtain cultures after the first case of the day, and after the second case. During the intervention period (ProvodineTM; usual hand hygiene practice), the investigators obtain hand cultures from the same anesthesia providers at the beginning of the day. The participants will then then do a hand scrub with ProvodineTM. The investigators will obtain a second hand culture at this point and participants will rinse and dry their hands to remove the culture medium and then apply a small amount of ProvodineTM as a hand rub. The investigators will obtain cultures after the first case of the day, and after the second case of the day. If participants are still providing anesthesia to their second case 6 hours after they applied ProvodineTM, the participants will apply a small of ProvodineTM amount as a hand rub at this time. For anesthesia providers in the ASC, the investigators will use the same protocol with the following exception. Because cases are likely to be shorter, the investigators will obtain the final cultures after the last case of the day or after the case that ends closest to 6 hours after ProvodineTM was applied in the morning.

NCT ID: NCT03992209 Completed - Hand Hygiene Clinical Trials

Reducing Intraoperative Infection Transmission in the Pediatric Operating Room

Start date: December 17, 2019
Phase: N/A
Study type: Interventional

Patients becoming infected during hospitalization occurs frequently and causes harm. It is important for healthcare facilities to take action to prevent these infections and their spread between patients. Despite the presumption of a "sterile" environment, one place where spread of infection is known to happen is in the operating room. This occurs as a result of frequent interaction among healthcare providers, the patient and the environment of the room. Hand washing is an important component of preventing the spread of infections. Scientific evidence has shown that making it easier for people to wash their hands can have two important impacts: (1) reduction of environmental bacterial contamination and (2) reduction in spread of bacterial pathogens. OR PathTrac is new technology that allows tracking of bacterial spread. While data exists about bacterial contamination and transmission in the adult operating room, there is very minimal data about this in the pediatric operating room. Primary aim: To use OR PathTrac to evaluate the effect of a personal hand washing device in reducing operating room exposure to bacterial pathogens in pediatric patients. We hypothesize that this hand washing system will decrease exposure to pathologic bacteria in the pediatric operating room. Secondary aim: To gain knowledge about baseline bacterial contamination and transmission in pediatric operating rooms. We will answer this question by comparing bacterial cultures taken from operating rooms whose personnel are trained to use the hand washing device to operating rooms who are not trained to use the device.