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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: NCT06180746 Not yet recruiting - Mediation Clinical Trials

Study of the Conditions of the Effects of Health Mediation on Underserved Population

ECEMSo
Start date: December 15, 2023
Phase: N/A
Study type: Interventional

The investigators are conducting a longitudinal mixed-method intervention study with a multi-center, multi-case explanatory sequential design. The ECEMSo study aims to identify the impact of health mediation on fostering healthcare utilization, in particular organized cancer screening uptake, by underserved populations living in informal housing in France.

NCT ID: NCT06180486 Recruiting - Clinical trials for Total Knee Replacement

Mindfulness Meditation Intervention Study

Start date: February 2, 2024
Phase: N/A
Study type: Interventional

The goal of this pilot study is to develop a randomized control trial study with sufficient power to definitely address if a preop mindfulness meditation intervention can improve post-total knee arthroplasty mental well-being or physical health compared to controls, and if a preop mindfulness meditation intervention can train resilience. The main questions it aims to answer are: 1. Is this preoperative mindfulness meditation study feasible at Hospital for Special Surgery? 2. Can we estimate a control and intervention group central tendency and variability to be used to determine sample size in future study? 3. Does a preoperative mindfulness meditation interventions improve post-total knee arthroplasty mental well-being or physical health compared to controls? Can preoperative a mindfulness meditation intervention train resilience (as measured by increased resilience score)? Participants will be randomly assigned to be in the intervention group or the waitlist control group. The intervention group gets the mindfulness mediation intervention prior to their day of surgery, and the control group will be given the mindfulness meditation intervention 90 days after their day of surgery. The waitlist control group allows for comparison between those who got the mindfulness meditation intervention prior to surgery and those who did not while still offering the potential benefits of the intervention after 90 days.

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.

NCT ID: NCT05760768 Completed - Clinical trials for Gestational Weight Gain

The Effect of Individualized Exercise Guidance on Pregnancy Outcome

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

A single center, randomized controlled trial was conducted to investigate whether individualized exercise guidance was more effective in improving pregnancy outcomes in normal pregnant women. What's more, the trial was also conducted to find out whether there is a mediating effect between prenatal exercise and pregnancy outcomes.

NCT ID: NCT04863690 Not yet recruiting - Mediation Clinical Trials

Assessing the Effects of the Muse Sleep Intervention on Sleep

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

In this study, we will examine whether use of the Sleep Intervention protocol marketed by Interaxon (the 'Muse'), leads to improvements in sleep quality (e.g. decreased latency to sleep, improved sleep duration), as well as knock-on improvements on measures of mindfulness, improvement in quality of life scores, reduction in perceived stress levels, anxiety, improvements in cognitive performance, improvement in markers relevant for safety, and increased success in the workplace in healthy participants.

NCT ID: NCT04301700 Active, not recruiting - COPD Clinical Trials

Effects of Progressive Muscle Relaxation and Mindfulness Meditation in Patients With Chronic Obstructive Pulmonary Disease

Start date: April 20, 2018
Phase: N/A
Study type: Interventional

Patients with COPD will be entered. Participants will be randomized to one of three study arms: Arm 1: meditation; Arm 2: relaxation; Arm 3: Control. Hypothesis: Progressive muscle relaxation and mindfulness meditation will decrease severity of dyspnea, fatigue and care dependency.

NCT ID: NCT04189146 Active, not recruiting - Depression Clinical Trials

Inner Engineering Yoga Program on Short and Long Term Health Effects (ISHA-Impact): A Longitudinal Study

ISHA-Impact
Start date: March 12, 2019
Phase: N/A
Study type: Interventional

This study will include any participant who registered, and plans to attend the Inner Engineering In-Person Completion Course. In 2019, this course was offered in: Los Angeles in March, Philadelphia in April and Toronto & Dallas in November. This study has been involved in every IECO Course since 2019 and is still active today. Beginning in August 2021, investigators will recruit for the August Inner Engineering In-Person Completion Course. Investigators anticipate that this study can include up to 5,000 study participants. Participants would attend this course and complete the pre-modules regardless of whether or not they participate in this study.

NCT ID: NCT03139110 Completed - Mediation Clinical Trials

Impact of a Mediator for Patient Intake in Emergency Departments

MEDIA
Start date: November 15, 2017
Phase:
Study type: Observational

Violence in the workplace is becoming a serious phenomenon in the contemporary world of work. Hospital staff, like any employee working in contact with the public, is particularly exposed to this violence. In emergency departments, the number of patients treated and their heterogeneity, the problems of communicating with healthcare professionals, and waiting times, favor conflict situations. In the already tense context of the emergencies, the incivilities or violent acts have an impact on the well-being of professionals. In order to prevent these situations of violence, a solution could be to integrate a professional with specific skills into the teams to perform mediation functions between caregivers and patients. The aim of the study is to evaluate the impact of the presence of a mediator in emergency services on personal (verbal or physical) attacks on professionals (caregivers, doctors, administrative staff).