PRMNURSEProgressive Muscle Relaxation Impact on Nursing Students' Mental Health and Biopsychosocial Responses
This study investigates how Progressive Muscle Relaxation affects nursing students' mental health and biopsychosocial responses. We will measure changes in depression, anxiety, and stress levels before and after a 4-week intervention using the Depression Anxiety Stress Scale - 21.
Progressive relaxation exercise
Psychological Well-Being+9
+ Anxiety Disorders
+ Behavior
Supportive Care Study
Summary
Study start date: January 1, 2025
Actual date on which the first participant was enrolled.Nursing students often deal with academic stress, emotional challenges, and clinical duties, which can result in psychological issues like depression, anxiety, stress, and worries about their future. These issues can impact their overall well-being and professional abilities. The study explores the use of progressive muscle relaxation exercises (PMRE), a recognized method for reducing muscle tension, managing stress, and improving emotional control, to help nursing students manage these challenges. This study, conducted between June 2024 and June 2025, involves nursing students who are randomly assigned to either an experimental group that receives PMRE or a control group. The impact of PMRE is measured using a pre-test-post-test design, with tools like the Depression, Anxiety and Stress Scale (DASS-21), the Future Orientation Scale, and the Biopsychosocial Response Scale for Nursing Students. The primary outcome of interest is the change in depression, anxiety, and stress levels, as measured by the DASS-21 scale at the beginning and end of the 4-week intervention period.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.104 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location