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Neurofeedback-mindfulness Techniques on Anxiety, Stress, and Academic Performance of Nursing Students

EFFECT OF NEUROFEEDBACK-MINDFULNESS TECHNIQUES ON ANXIETY, STRESS, AND ACADEMIC PERFORMANCE OF NURSING STUDENTS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07234006
Enrollment
36
Registered
2025-11-18
Start date
2025-11-21
Completion date
2026-05-31
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Academic Performance, Anxiety, Stress

Brief summary

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.

Interventions

BEHAVIORALNEUROFEEDBACK-MINDFULNESS

The 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.

OTHERNo intervention

No intervention

Sponsors

University of Salamanca
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* 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.

Exclusion criteria

* History of serious psychiatric disorders in the 6 months prior to inclusion in the study.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in the Mean of the Depression, anxiety and stress scale at 4 weeksFrom enrollment to the end of treatment at 4 weeksZero is equivalent to no symptoms and 63 indicates the worst possible symptoms
Change from Baseline in the Mean Academic performance score at 4 weeksFrom enrollment to the end of treatment at 4 weeksZero is equivalent to the best academic performance and 40 indicates the worst academic performance

Countries

Spain

Contacts

CONTACTJosé Ignacio Recio Rodriguez, Doctor
donrecio@usal.es+34650330694

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026