Neurofeedback-mindfulness Techniques on Anxiety, Stress, and Academic Performance of Nursing Students
NCT ID: NCT07234006
Last Updated: 2025-12-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
36 participants
INTERVENTIONAL
2025-11-21
2026-05-31
Brief Summary
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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.
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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No intervention
No intervention
No intervention
No intervention
NEUROFEEDBACK-MINDFULNESS
Neurofeedback-Assisted Mindfulness Training Program
NEUROFEEDBACK-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.
Interventions
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NEUROFEEDBACK-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.
No intervention
No intervention
Eligibility Criteria
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Inclusion Criteria
* Aged between 18 and 45 years
* Willing to voluntarily participate in the study and sign the informed consent form.
Exclusion Criteria
18 Years
45 Years
ALL
Yes
Sponsors
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University of Salamanca
OTHER
Responsible Party
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José Ignacio Recio Rodriguez
Doctor
Locations
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Faculty of Nursing
Salamanca, , Spain
Countries
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Central Contacts
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Facility Contacts
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Jose I Recio-Rodriguez
Role: primary
Other Identifiers
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25CO1/005243
Identifier Type: -
Identifier Source: org_study_id