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NCT ID: NCT05948670 Completed - Clinical trials for Satisfaction, Personal

Participant Satisfaction With the BUILD Mobile Application

Start date: October 4, 2023
Phase: N/A
Study type: Interventional

This study explores user satisfaction with the BUILD mobile application.

NCT ID: NCT05597514 Completed - Clinical trials for Satisfaction, Personal

Three-dimensional Airway Suction Model

Start date: February 22, 2023
Phase: N/A
Study type: Interventional

The main purpose of this study is to use 3D printing technology to high-fidelity simulation respiratory models Furthermore, the results of this study will extent to medical school and hospital.

NCT ID: NCT05410236 Completed - Clinical trials for Satisfaction, Personal

3D Printing in Airway Anatomy and Bronchoscopy Education

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

The main purpose of this study is to use 3D printing technology to make a human anatomical bronchial tree model, which is applied in medical education for medical students and students of the department of respiratory therapy. Most of the clinical teaching material is expansive and inaccessible. To promote accessibility of anatomy models and student learning effects in our school and hospital, we use the 3D printing technology to print bronchial tree model and apply it to anatomy and bronchoscopy education. The present study expects some benefits that the use of printed bronchial trees for anatomy and bronchoscopy education. For example, it can reduce the cost of anatomy instruction, let students have their own anatomical model, and make the learning no longer limited to the anatomical classroom.

NCT ID: NCT05207891 Completed - Pain Clinical Trials

Comparing Pressure Injury Occurrence in Patients Using Two Different Mattresses

Start date: September 14, 2021
Phase: N/A
Study type: Interventional

The purpose of this project is to compare a newly developed automatic reversing dynamic air mattress, with a regular care mattress, which is in daily use at the hospital. Focus will be on pressure relief in relation to occurrence of pressure injury, user satisfaction, and the mattresses impact on sleep and pain. The participants will be randomized to start with the intervention mattress or the control mattress. Outcomes will be measured via validated forms regarding pressure related injuries, quality of life, pain, and mattress comfort. Custom made forms will be used regarding resource use and comfort in the nursing service, especially in relation to position changes in the participants .

NCT ID: NCT05193955 Completed - Stress Clinical Trials

The Effect of Laughter Yoga Practiced Before Simulation Training

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

Simulation education has become one of the innovative educational approaches that are widely used in providing nursing students with knowledge, skills, and attitudes towards vocational courses. Simulation education provides students with the opportunity to combine their knowledge and skills and provide nursing care in a high-reality environment. However, the fact that simulation training is a method that requires the student to recognize a clinical event, make a clinical decision, and intervene with the patient in line with this decision may cause students to experience anxiety and affect their learning. Although there are limited studies conducted on nursing students, it is stated that new approaches such as laughter yoga are effective in reducing anxiety and stress levels. In this direction, this research; In this study, it was planned to investigate the effectiveness of laughter yoga in terms of reducing the anxiety experienced by nursing students during simulation training and increasing their learning satisfaction. The universe of the research will be the second-year students of Hacettepe University Faculty of Nursing. As a result of the power analysis, it is aimed to reach 54 people. The study was planned in a randomized controlled design. Research data will be collected through Personal Information Form, State Anxiety Scale, Student Satisfaction and Self-Confidence in Learning Scale, Perceived Stress Scale for Nursing Students, and Students' Vital Findings Evaluation Form. With this study, it is predicted that laughter yoga to be applied to nursing students before simulation training will have a positive effect on state anxiety, student satisfaction, and perceived stress level.

NCT ID: NCT04391075 Completed - Urinary Retention Clinical Trials

Analgesia in the Second Stage of Labour

ASL
Start date: January 1, 2017
Phase:
Study type: Observational [Patient Registry]

This study investigates efficacy, safety and childbirth experience in women receiving pudendal block during the final stage of delivery. It is an observational study and half of included primarous women recieve a pudendal block.

NCT ID: NCT03940534 Completed - Clinical trials for Medication Adherence

Utilization of the TAD Device for Dispensing Pain Medications in Hospice Patients

Start date: March 9, 2018
Phase: N/A
Study type: Interventional

A novel device, TAD, has been developed to aid adherence to prescribed regimens and may have a roll in hospice pain management. This study aims to assess medication adherence relating to missed doses or improperly timed doses with and without the aid of a mobile device as a primary endpoint. Secondary endpoints will be patient, nursing, and provider satisfaction.

NCT ID: NCT03775876 Completed - Sedation Clinical Trials

Dexmedetomidine Versus Propofol in Conjunction With Regional Block for Shoulder Arthroscopy

Start date: March 1, 2017
Phase: Phase 4
Study type: Interventional

Operative shoulder arthroscopy under regional block anesthesia often presents with hemodynamic challenges for the anesthesiologist, knowing that a low systolic blood pressure is required to minimize the bleeding. Regional anesthesia is successfully performed to many patients in whom tracheal intubation or the placement of a laryngeal tube is undesired. Propofol has traditionally been used to provide sedation in patients undergoing shoulder arthroscopy under regional anesthesia. In contrast to Propofol, Dexmedetomidine is a highly selective α-2 adrenoceptor agonist that has been shown to provide sedation, analgesia and anxiolytic effects with minimal respiratory depression. Due to the effect of both drugs on blood pressure, the investigators set out to compare intraoperative hemodynamics of both drugs, along with the surgeon's satisfaction and the degree of comfort provided to patients undergoing interscalene brachial plexus block for shoulder arthroscopy. The investigators also assessed whether the type of anesthetic agent used for sedation accounted for other differences in intra and post-operative outcome measures.

NCT ID: NCT03521453 Completed - Anesthesia Clinical Trials

PEPPER : PErcePtion of Pre-anesthesia Visit With or Without Robot

PEPPER
Start date: April 15, 2018
Phase:
Study type: Observational

Pre-anesthesia visit for scheduled surgery is mandatory by law in France. During this visit, patients should be informed of the different available technics of anesthesia (i.e. general or loco-regional) and of their own risks . Nowadays, many informations are given through written paper and leaflets, just before the consultation. In addition, patients need usually to wait for the doctor. This time may be used to give information, and new information's support, such as videos, may be used. The aim of this study is to evaluated if a robot (PEPPER), who is able to answer to patients and to give informations, may increase the satisfaction of patients having a pre anesthesia visit for a scheduled surgery.

NCT ID: NCT03372889 Completed - Clinical trials for Anterior Cruciate Ligament Injury

On-Q Catheter Caregiver Education

Start date: July 11, 2017
Phase: N/A
Study type: Interventional

The present study aims to compare caregiver satisfaction and efficacy between two modes of patient education materials (PEMs): media based and print based. The caregivers of patient's who undergo ACL (anterior cruciate ligament) reconstruction surgery and receive an On-Q Catheter pain block receive both a hand-out (print based PEM) and watch a short video (media-based PEM) describing how to care for their child's On-Q Catheter at home. Upon enrollment into the study, caregivers are randomly assigned to either first view the hand-out or the video, then complete a 10 questions standardized assessment of information that was presented in the PEMs. Caregivers are called the next day to assess caregiver satisfaction with the PEMs, which mode of PEM was more helpful to them, and how comfortable they felt managing their child's pain pump at home.