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NCT ID: NCT06202352 Enrolling by invitation - Mediation Clinical Trials

Basic Yoga and Meditation Techniques

Start date: February 15, 2024
Phase: N/A
Study type: Interventional

Purpose of the research; To determine the effect of basic yoga techniques and meditation intervention on midwifery students' anxiety and perceived stress levels. Yoga is alternative mind-body exercises that aim to establish a connection between the brain and body. Derived from the Sankiritic term "yuj", yoga means to integrate. Yoga techniques focus on self-awareness and require careful coordination of body movements/postures (asanas), deep breathing (pranayama) and meditation. Yoga can be used as a complementary and alternative method for various diseases or improving well-being. Yoga is becoming increasingly important in improving mental health. In this planned study, we aim to manage the anxiety and perceived stress that students studying in the field of health mostly suffer from with yoga techniques. After the sociodemographic data of the volunteer participants who agree to take part in the research are identified and recorded in the first stage, the screening phase, according to the power analysis, the minimum number of participants determined will be assigned to the experimental and control groups by randomization. In the second stage of the research, the experimental group; Yoga techniques and meditation practices (once a week for 8 weeks) will be performed at times when anxiety and stress are most intense (before exams, laboratory and hospital applications). Students in the control group will continue their routine coping habits with anxiety and stress. Students will complete pre- and post-intervention surveys to assess changes in anxiety and perceived stress. The anxiety and stress levels of students in both groups will be determined by applying the "Beck Anxiety Inventory" and the "Perceived Stress Scale" before and after the intervention. The data obtained after the interventions will be compared with appropriate statistical analysis and converted into a report. The proposed research aims to provide scientific research skills and experience to the 2nd year students of Atatürk University, Faculty of Health Sciences, Department of Midwifery, who are involved in the project. In addition, it is expected that the proposed project will show how it affects the anxiety and perceived stress levels of midwifery students in the international media and literature and emphasize its positive effects on the management of the well-being of these individuals.

NCT ID: NCT05804838 Enrolling by invitation - Depression Clinical Trials

Investigation of the Effect of Mindfulness-Based Stress Reduction Program on in Pregnant Women

Start date: June 6, 2023
Phase: N/A
Study type: Interventional

This study was planned to examine the effects of the Mindfulness-Based Stress Reduction Program, which is one of the popular concepts of the 21st century, on depression, psychological well-being and prenatal attachment, which are likely to occur as a result of increased stress during an important period that requires adjustment as a result of physical, mental and cognitive changes during pregnancy. It will be conducted in a randomized parallel controlled experimental design type using Consolidated Standards of Reporting Trials (CONSORT) guidelines. It is planned to be carried out with the ZOOM Cloud Meetings program, which is an online education platform, with pregnant women who apply to the Health Sciences University Ümraniye Training and Research Hospital pregnancy polyclinic in the Ümraniye district of Istanbul. The universe of the research will be the pregnant women who applied to the Health Sciences University Ümraniye Training and Research Hospital pregnant outpatient clinic. Primiparous pregnant women who meet the inclusion criteria and willingly agree to participate in the study will be included in the study. 54 people in the intervention group, 54 people in the control group, and a total of 108 people will be taken. While the Conscious Awareness-Based Stress Reduction Program adapted for pregnant women will be applied to the intervention group, routine follow-up will be applied to the control group within the scope of the outpatient clinic follow-up of the relevant institution. Informed Voluntary Consent Form, Descriptive Characteristics Information Form, Psychological Well-Being Scale, Beck Depression Scale, Prenatal Attachment Scale and Conscious Awareness Scale will be administered to the participants included in the study. As a result of the findings, the discussion and results of the study will be written.