Remote Assessment of Digital Neurologic Testing (RADiaNT)

Mayo Clinic

Status: Enrolling

Conditions: Neurology

Treatments: Behavioral: Guided Meditation

Study type: Interventional

Funder types: Other

Identifiers

NCT07014982

24-013687

Details and patient eligibility

About

The RADiaNT study investigates whether guided meditation, using the Muse™ headband and biofeedback app, can improve sleep, mood, and cognitive performance, aiming to assess its impact on mental and emotional well-being.

Enrollment: 40 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Cognition unimpaired or mild cognitive impairment
• Fluent in English
• United States resident
• Able to tolerate wearing Muse headband
• basic competence in using electronic devices (Smartphone or tablet) to engage with the Muse application and complete digital surveys and assessments

Exclusion criteria

• Neurological and Brain Disorders
• Not Fluent in English
• Not a US Resident
• Unable to tolerate wearing Muse Headband

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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40 participants in 2 patient groups

Guided Meditation

Experimental group

Description:

This cohort will be practicing guided meditation for 5 days/week, five minutes a day for 6 weeks. Then there will be a period of testing followed by another 6 week period of practicing guided meditation.

Treatment:

Behavioral: Guided Meditation

Standard of Care

No Intervention group

Description:

This cohort will be asked to complete neurologic testing at baseline, interim, and conclusion periods while conducting NO guided meditation throughout the duration of the study.