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Effectiveness of Heart Rate Variability Biofeedback Training Versus a Meditation Program in Reducing Stress Levels in University Undergraduate Students.

U

University of Seville

Status

Not yet enrolling

Conditions

Anxiety State
Stress

Treatments

Behavioral: Heart rate variability biofeedback training
Behavioral: Guided meditation

Study type

Interventional

Funder types

Other

Identifiers

NCT06457932
77859612N

Details and patient eligibility

About

The objective of this trial is to evaluate the efficacy of a heart rate variability biofeedback training protocol, compared to a guided meditation program and a control group, in reducing stress and anxiety levels among university undergraduate students.

Enrollment

54 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Second- and third-year students of the Physiotherapy Degree at various universities in the province of Seville.
  2. Enrolled in all courses for the academic year.
  3. Enrolled in the courses for the first or second time.

Exclusion criteria

  1. Having a job in addition to academic responsibilities.
  2. Having a dependent family member under their care.
  3. Diagnosed with any mental health issues.
  4. Diagnosed with severe metabolic, cardiovascular, or respiratory conditions, or cancer.
  5. Simultaneously pursuing another degree or a dual degree program.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 3 patient groups

Biofeedback training
Experimental group
Description:
An 8-week intervention based on daily 10-minute HRV biofeedback training at rest using the Pulse HRV smartphone application.
Treatment:
Behavioral: Heart rate variability biofeedback training
Meditation
Active Comparator group
Description:
An 8-week intervention based on daily 10-minute guided meditation sessions led by an instructor with over 20 years of experience in teaching meditation.
Treatment:
Behavioral: Guided meditation
Control
No Intervention group
Description:
Passive, waitlist control group.

Trial contacts and locations

0

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Central trial contact

Hermann Fricke-Comellas, PhD Student

Data sourced from clinicaltrials.gov

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