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NCT ID: NCT06046378 Completed - Education Clinical Trials

The Effect of Digital Stories Prepared With Digital Audio File (Podcast) on Midwifery Learning

Start date: October 3, 2022
Phase: N/A
Study type: Interventional

This study was conducted as a randomized controlled study to determine the effect of digital stories prepared with a digital audio file (podcast) on learning in midwifery education. The study was carried out with Kocaeli University Midwifery 3rd grade students. Between October 3 and October 7, 2022, which is the beginning of Kocaeli University 2022-2023 academic year academic calendar, a meeting was held with students about working outside the classroom. The study was completed with 65 students as experimental (n=33) and control group (n=32). Data were collected with participant information form, knowledge test, digital stories evaluation questionnaire prepared with digital audio file (podcast). These stories, which consist of three parts about preparation for natural birth, ideal birth environment and natural birth, were recorded in an appropriate environment and quality, accompanied by a trainer who is an expert in digital audio files (podcast) designs. The knowledge test was applied as a pre-test in the first encounter with the students who accepted the study. Digital stories were sent to the students in the experimental group in the form of e-mails. At the end of the unit, a post-test was administered to both groups. Again, 21 days later, the study was completed by conducting a retention test (knowledge test) and a digital story evaluation questionnaire prepared with a digital audio file (podcast) for both groups. After the study, digital stories prepared with a digital audio file (podcast) were sent to all students in the control group who completed the study, allowing the students to reinforce the subject. While evaluating the findings in the study, Number Cruncher Statistical System 2020 Statistical Software (NCSS LLC, Kaysville, Utah, USA) program was used for statistical analysis. While evaluating the research data, quantitative variables were shown with mean, standard deviation, median, min and max values, and qualitative variables were shown with descriptive statistical methods such as frequency and percentage. Shapiro Wilks test and Box Plot plots were used to evaluate the suitability of the data for normal distribution. Student's t-test, Mann Whitney-U test, Kruskal Wallis test, Dunn test, Spearman correlation analysis, linear regression, chi-square test, Fisher's Exact test, Isher's Exact test and Fisher Freeman Halton and F test were used. The results were evaluated at 95% confidence interval and p<0.05 significance level.

NCT ID: NCT06015984 Not yet recruiting - Clinical trials for Kidney Transplantation

Renal Transplantation Nurse Training on Patient-Centered Care Competence and Counseling Skills

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

There are two main treatments for end-stage renal disease (ESRD): dialysis and transplantation.Renal transplantation is the best and most preferred treatment for ESRD patients.Self management after renal transplantation is difficult. Individuals need appropriate care,education, counseling and support in order to change their behavior to cope with health problems during the transplantation process.The aim of nursing care and education is to enable the individual to acquire the knowledge, skills and attitude to independently carry out daily life activities and to adopt this as a lifestyle.Nursing care and education requires an interdisciplinary teamwork, and in this process, the nurse plays a key role as she constantly interacts with the donor, recipient and family.The research was designed as a randomized controlled experimental study with pretest-posttest design.A total of 60 nurses, 30 in the control group and 30 in the intervention group,who met the criteria for inclusion in the study, will form the sample of the study.After obtaining consent from the nurses in the intervention and control groups, they will be asked to fill out the Nurse InformationForm, the Patient-Centered Care Competency Scale and the Nurses Counseling Skills Scale. Aftercompleting the web-based training, intervention group nurses will be asked to fill in the Patient Centered Care Competency Scale and the Counseling Skills in Nurses Scale at the 1st and 3rd months. No training will be given to the nurses in the control group and they will be asked to fill the Patient-Centered Care Competency Scale and the Counseling Skills for Nurses Scale again.

NCT ID: NCT06005025 Recruiting - Breast Cancer Clinical Trials

Examination of the Effect of Counselling and Follow-up After Breast Cancer Awareness Education

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

The aim of the study was to examine the effect of counselling and follow-up after education on the risks and prevention methods of breast cancer on early diagnosis behaviours and healthy lifestyle behaviours. The population of the study will consist of female administrative staff working at Mersin University. The sample of the study will consist of 160 people. A total of 160 personnel determined by randomisation will be divided into group A (study) and group B (control) formed by the independent researcher in the computer environment. All participants will be given a one-hour training on breast cancer and will be practised with a model as well as a presentation. Group A will be counselled for 6 months after the training and a reminder message will be sent via SMS on Monday every week as "Check your modifiable risk factors for breast cancer" and their feedback will be received. In group B, no additional application will be made except for the training. The data of the study will be collected before and 6 months after the training by using the Descriptive Characteristics Form, Breast Cancer Early Diagnosis Behaviours Form, Counselling Form and Healthy Lifestyle Behaviours Scale II. The data obtained from the study will be analysed in a computer environment. Number, percentage, mean and standard deviation will be used as descriptive statistics in the evaluation of the data.

NCT ID: NCT05998681 Completed - Education Clinical Trials

Effects of Education on Breastfeeding

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

Objective: This study aims to investigate the effectiveness of education on breastfeeding and basic maternal-neonatal care and mobile message support given to primiparous women in the postpartum period on breastfeeding and motherhood experiences. Methods: This prospective randomized controlled study was conducted in a hospital located in a city in Turkiye, with 130 primiparous patients in the postpartum period (65 individuals in the experimental group and 65 individuals in the control group). Participants in the experimental group were provided with education on "Breastfeeding and Basic Maternal-Neonatal Care" at the hospital and mobile messages were sent with the same content as education program for 6 weeks after discharge.

NCT ID: NCT05974943 Completed - Education Clinical Trials

The Effect of Problem Solving and Decision Making Training Given to Nurses Managers

Start date: October 10, 2022
Phase: N/A
Study type: Interventional

This research was conducted to evaluate the impact of the Problem Solving and Decision Making Training program, which was developed to enhance the problem-solving and decision-making skills of nurse managers at the lower, middle, and upper levels, by the subordinates and superiors of nurse managers. To assess the problem-solving and decision-making skills of nurse managers as perceived by their subordinates, the Problem-Solving Inventory-Managerial Version (PSI-MV) and Decision-Making Styles Scale-Managerial Version (DMSS-MV) underwent adaptation, validity, and reliability studies. These studies aimed to enable the evaluation of nurse managers' problem-solving and decision-making abilities from the perspective of their subordinates.

NCT ID: NCT05974891 Recruiting - Education Clinical Trials

The Effect of Simulation-Based Experience on Nursing Students

Start date: February 26, 2024
Phase: N/A
Study type: Interventional

This research was planned as a randomized controlled experimental study to determine the effect of simulation training on the acquisition of self-awareness and empathy skills in nursing students.

NCT ID: NCT05951660 Recruiting - Schizophrenia Clinical Trials

Sex, Psychopharmacology, and Diabetes

SECRET
Start date: August 24, 2023
Phase: N/A
Study type: Interventional

The term sexual (SD) dysfunction covers conditions that prevent people from having a satisfactory sex life. SD is a frequent and sometimes debilitating complication of mental illness and a known adverse reaction to psycho-pharmacological treatment. SD is also associated with diabetes, a common somatic comorbidity in psychiatric patients. SD is associated with both reduced quality-of-life and reduced treatment adherence, yet SD is far too rarely addressed between the patient and the healthcare professional in clinical consultations. The purpose of the study is to investigate whether targeted education of patients with schizophrenia and diabetes/prediabetes and/or their healthcare professionals in causes and management of SD: - Increases the number of systematic examinations of sexual side effects, - Causes changes in the psycho-pharmacological treatment, and - Reduces the severity or perception of sexual side effects. The study is a multicenter Randomized Controlled Trial (RCT) with four arms, in which the educational intervention is provided to patients, healthcare professionals, or both groups. The effect of the educational intervention is compared to a non-educated control group. The study is expected to include 192 patients recruited from 16 assertive community treatment centers evenly distributed in four Danish regions. The study is part of an interdisciplinary project named SECRET. The educational intervention was developed in an ethnographic pre-study incorporating stakeholder engagement. Parallel to the present RCT, an ethnographic field study will be carried out to broaden the perspective on the effects of the intervention.

NCT ID: NCT05951088 Recruiting - Education Clinical Trials

Long-term Evaluation of a Mobile Application for Follow-up of Cardiac Patients (Cardio2U Study)

Cardio2U
Start date: May 23, 2023
Phase:
Study type: Observational

This trial has to aim to evaluate an innovative, in-house developed mobile application supporting patients in their home environment by actively involving them in different aspects of their condition and treatment. The usability, long-term adherence and patient satisfaction will be studied in patients with atrial fibrillation (AF) and/or heart failure (HF).

NCT ID: NCT05941026 Completed - Education Clinical Trials

Developing Nursing Students' Intercultural Sensitivity Levels

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

This study; This is a randomized controlled experimental type study designed to improve the intercultural sensitivity levels of nursing students.

NCT ID: NCT05928117 Completed - Pregnancy Clinical Trials

Training Given in the Line of Coping With Fear of Birth on Fear of Birth Birth Experience

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

Pregnancy and childbirth are a natural life event for women, as well as a process in which physical, biological and psychosocial changes are experienced. This process causes women to perceive childbirth as an unknown and unpredictable situation, resulting in the fear of childbirth. Due to the fear of childbirth, the daily routines, professional lives, social activities and relationships of pregnant women are significantly affected. This study was planned to evaluate the effect of mobile education given in line with the "Guide to Coping with Fear of Birth" on fear of birth, birth preference and maternal satisfaction at birth. Research; It will be carried out at the T. C. Ministry of Health Gaziantep Cengiz Gökçek Gynecology and Pediatrics Hospital. Data; The first one is 28-30th of pregnancy. week, the second is 36-38. It will meet in three meetings in total, the third of which will be within 12-24 hours postpartum. Data, Personal Information Form (Annex-1), Wijma Birth Expectation/Experience Scale (W-DEQ) Version A (Annex-2), Wijma Birth Expectation/Experience Scale Version B (Annex-3) and Birth Experience Scale ( Annex-4) and Postpartum Questionnaire (Annex-5). The obtained data will be analyzed with the SPSS 22.0 program. In this study, it is thought that the training given to women with a high level of birth fear can reduce their fear of childbirth and increase maternal satisfaction at birth.