What is the attainability of a study examining the stress-reducing effect of a new neurofeedback device?

Completed

• Conditions: Het heeft niet betrekking op mensen met een aandoening: gezonde vrijwilligers die meer dan gemiddeld gestresst zijn maar verder gezond, zijn de doelgroep; Healthy volunteers

• Registration Number: NL-OMON31743
• Lead Sponsor: Philips Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 12 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

1) A score of at least 1 standard deviation above the reported mean of the Perceived Stress Questionnaire
2) 18 - 30 years old
3) Written informed consent

Exclusion Criteria

1) Evidence of a significant psychiatric (e.g. sleep disorder or major depression), neurological (e.g. epilepsy) or other medical (particularly cardiovascular and adrenocortical) disorder at the time of inclusion
2) Pregnancy at the time of inclusion (based on the subjective report of the subject)
3) The excessive use of medication, particularly corticosteroid medication at the time of inclusion
4) Significant alcohol abuse at the time of inclusion
5) An education level that is lower than high school
6) With occurrence of certain medical diseases (for example fever) a subject can be temporarily be excluded from the intervention

Study & Design

• Study Type: Interventional
• Study Design: Not specified