Skip to main content
Clinical Trials/NCT03895190
NCT03895190
Completed
Not Applicable

Effects of a Application (Flourish App) on Stress, Well-being and Emotional Regulation in Medical Students

Hospital Israelita Albert Einstein1 site in 1 country50 target enrollmentAugust 6, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Emotional Stress
Sponsor
Hospital Israelita Albert Einstein
Enrollment
50
Locations
1
Primary Endpoint
Changes in subjective symptoms of well-being at work
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This protocol proposes a well-being program, delivered through an application for mobile devices, based on meditation and positive psychology principles such as human development, the improvement of virtues, quality of life and well-being. The investigators hypothesize that this program offered in mobile application may promote well-being, reduce stress related problems and improving emotional regulation in the participants. Objectives: To evaluate the effectiveness of a well-being program delivered through an application for mobile devices in a sample of medical students. Methods: Three hundred students of the undergraduate medical course of Albert Einstein Israelite Faculty will be recruited. The participants will be randomized in two groups of 150 participants each one, half of them in the control group (GC) and the other half to the intervention group (GI).

Detailed Description

INTRODUCTION: One population that presents an important vulnerability to stress is that of university students, facing several stressors, such as academic demands, time pressure and social adjustments. Medical students in particular may face additional challenges such as heavy workload, time commitment and the number of tests and assessments as well as the pressures of a clinical setting. Some highly successful programs in stress management are based on the principle of Mindfulness. On the other hand, Positive Psychology brings a new paradigm in terms of mental and emotional health, seeking to promote human development through the development of virtues, quality of life and well-being, instead of just treating disease. In the modern world not all people are willing to attend classroom training for several reasons. In this sense, a program offered in mobile application can be considered an interesting alternative for professionals that not only want to reduce stress-related symptoms, but also promote well-being. MAIN OBJECTIVES: Evaluate the effects of a well-being program compared to a control program, both served on mobile applications, in reducing stress, increasing well-being and improving emotional regulation in a sample of medical students. METHOD: For this purpose, 300 students of the undergraduate medical course of Albert Einstein Israelite Faculty. Participants will be randomized into groups of 150 each, half to the control group (CG) and the other half to the intervention group (IG). The IG will participate in the Flourish App Program, for 8 weeks, while the CG will have access to a control application. Then, after the evaluations, the CG will participate in the Flourish App Program, while the first group will not participate in any intervention. Before starting the program, after 4 and 8 weeks of the program, questions will be applied to assess the stress and well-being levels of participants in general and in relation to work. In addition, before and after each training period, questions will be applied to assess the stress and well-being levels of participants at the moment. Also, the Perceived Stress Scale, the 5-item World Health Organization Well-Being Index - WHO-5, the Mindful Attention Awareness Scale, the Self-Compassion Scale and the Difficulties in Emotion Regulation Scale will be applied too. Finally, at the end of the program, the Mobile Application Rating Scale - MARS will be applied.

Registry
clinicaltrials.gov
Start Date
August 6, 2019
End Date
April 21, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Women and men from 17 years
  • Students of the undergraduate medical course of Albert Einstein Israelite Faculty

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Changes in subjective symptoms of well-being at work

Time Frame: baseline, 4 weeks, 8 weeks

Sliding scale for stress level from 0 to 100

Changes in subjective symptoms of stress

Time Frame: baseline, 4 weeks, 8 weeks

Sliding scale for well-being level from 0 to 100

Secondary Outcomes

  • Changes in subjective symptoms of stress at the moment assessed using the sliding scale for stress(four times a week, before and after the period of each class (20 minutes))
  • Changes in subjective symptoms of well-being at the moment assessed using the sliding scale for well-being(four times a week, before and after the period of each class (20 minutes))

Study Sites (1)

Loading locations...

Similar Trials