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Effectiveness of Neurofeedback on psychological stress

Evaluation of the effectiveness of Neurofeedback on psychological stress; salivary cortisol and a-amylase level in college students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190602043790N3
Enrollment
60
Registered
2024-02-02
Start date
2021-08-06
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Condition 1: Anxiety. Condition 2: stress. Anxiety disorder due to known physiological condition Acute stress reaction

Interventions

Intervention 1: Control group: Participants do not receive intervention during the 12 weeks. Intervention 2: Intervention group: Participants receive 2 30-minute neurofeedback training session (The EE
Montreal, Quebec) transmite the signal to the computer. The EEG serves both as a means of recording and as a source for feedback, with a sampling rate of 256 Hz samples/second, and the data was redire

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: Achieving a score above 18 on the stress scale of the Stress, Anxiety and Depression Questionnaire (DASS-21) Age range between 18 to 25 years old

Exclusion criteria

Exclusion criteria: Presence or history of severe psychiatric disorders (including periods of severe depression, anxiety disorders, substance use disorders) Smoking and psychedelic pills Using psychiatric drugs Epilepsy Various cardiovascular and respiratory disorders and blood pressure Aspirin use and acetaminophen over the past 48 hours history of cancer diabetes hypothyroidism or hyperthyroidism Addison disease Cushing's syndrome hypertension Use of corticosteroids and steroids

Design outcomes

Primary

MeasureTime frame
Anxiety symptoms. Timepoint: At the beginning of the study (before the intervention), weeks 5 and 10 after the start of neurofeedback in intervention group. Method of measurement: Stress, anxiety and depression scales (DASS-21).;Stress. Timepoint: At the beginning of the study (before the intervention), weeks 5 and 10 after the start of neurofeedback in intervention group. Method of measurement: Stress, anxiety and depression scales (DASS-21).;Cortisol. Timepoint: At the beginning of the study (before the intervention), weeks 5 and 10 after the start of neurofeedback in intervention group. Method of measurement: Stress, anxiety and depression scales (DASS-21).;a amylase. Timepoint: At the beginning of the study (before the intervention), weeks 5 and 10 after the start of neurofeedback in intervention group. Method of measurement: Stress, anxiety and depression scales (DASS-21).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaba Hasanvandi

Bagheiat-allah University of Medical Sciences

s.hasanvandi@alzahra.ac.ir+98 21 8804 0060

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026