Neurofeedback-mindfulness Techniques on Anxiety, Stress, and Academic Performance of Nursing Students
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-45
SponsorUniversity of Salamanca
About this trial
In today's society, anxiety and stress are prevalent emotional responses in mental health globally, significantly affecting students' well-being and academic performance. In particular, undergraduate nursing students face high levels of these problems due to the heavy academic workload and demands of their training, especially during exam periods. The need for concentration, emotional management, and decision-making under pressure contribute to the prevalence of these disorders, impacting both their quality of life and academic performance.
Despite the existence of multiple strategies and techniques for managing these issues, it is still necessary to continue exploring innovative alternatives that complement traditional interventions. For this reason, this project aims to evaluate the effectiveness of mindfulness-neurofeedback as a treatment to reduce stress and anxiety in nursing students, with the goal of providing scientific evidence on this intervention. This brain training technique is presented as a promising option, based on the modulation of brain activity, with the potential to improve emotional regulation and concentration in the educational setting.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Students enrolled in the nursing degree at the University of Salamanca
Aged between 18 and 45 years
Willing to voluntarily participate in the study and sign the informed consent form.
Disqualifiers
History of serious psychiatric disorders in the 6 months prior to inclusion in the study.
Trial design
Design model
Parallel
Treatments tested in this trial
NEUROFEEDBACK-MINDFULNESS
BehavioralThe Neurofeedback-Assisted Mindfulness Training sessions will be given to the intervention group participants after randomization. Each session will vary in length depending on the session, but will last a maximum of 20 minutes. A total of 20 sessions will be held at the participant's home, preferably in the afternoon, at a rate of 5 sessions per week for 4 weeks after randomization. The organization of the sessions is described in the following table of this study's protocol.
No intervention
Other interventionNo intervention
Treatment groups
36 Participants
are divided into 2 treatment groupsGroup A: No interventionOther 1 intervention
Group B: NEUROFEEDBACK-MINDFULNESSExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Change from Baseline in the Mean of the Depression, anxiety and stress scale at 4 weeks
Zero is equivalent to no symptoms and 63 indicates the worst possible symptoms
Time frame
From enrollment to the end of treatment at 4 weeks2
Change from Baseline in the Mean Academic performance score at 4 weeks
Zero is equivalent to the best academic performance and 40 indicates the worst academic performance
Time frame
From enrollment to the end of treatment at 4 weeksSponsors and contacts
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Source ClinicalTrials.gov