Actively Recruiting

Phase Not Applicable
Age: 60Years - 85Years
All Genders
Healthy Volunteers
NCT06633978

Studying the Effects of Digital Interventions on Cognition, Wellbeing, Stress, and Sleep in Older Adults

Led by University of California, San Francisco · Updated on 2026-02-24

90

Participants Needed

1

Research Sites

98 weeks

Total Duration

On this page

Sponsors

U

University of California, San Francisco

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this proposed research is to collect pilot data to test the hypothesis that treatment with a novel form of closed-loop digital meditation (MediTrain) will lead to a greater magnitude of gains in cognitive abilities in patients with mild cognitive impairment (MCI), compared to OA without cognitive impairment, and will lead to improvements in quantitative measures of sleep.

CONDITIONS

Official Title

Studying the Effects of Digital Interventions on Cognition, Wellbeing, Stress, and Sleep in Older Adults

Who Can Participate

Age: 60Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Between 60 and 85 years old
  • Comfortable walking and in good physical health
  • Normal or corrected vision
  • Normal hearing
  • Fluent in spoken English
Not Eligible

You will not qualify if you...

  • History of neurological or psychiatric disorders
  • History of substance abuse
  • Taking anti-depressant or anti-anxiety medications
  • History of seizures
  • Color blindness
  • Glaucoma
  • Macular degeneration
  • Amblyopia (lazy eye)
  • Strabismus (cross eyed)
  • Presence of aneurysm clips
  • Cardiac pacemaker or implanted cardioverter defibrillator
  • Any electronic, magnetically-activated, or neurostimulation implants or devices
  • Spinal cord stimulator or internal electrodes/wires
  • Bone growth or bone fusion stimulators
  • Cochlear, otologic, or other ear implants
  • Insulin or other infusion pumps
  • Implanted drug infusion devices
  • Any type of prosthesis (eye, penile, etc.)
  • Heart valve prosthesis
  • Eyelid spring or wire
  • Artificial or prosthetic limbs
  • Metallic stents, filters, or coils
  • Shunts (spinal or intraventricular)
  • Vascular access ports or catheters
  • Radiation seeds or implants
  • Swan-Ganz or thermodilution catheters
  • Medication patches (e.g., Nicotine, Nitroglycerine)
  • Metallic fragments or foreign bodies in/on the body that cannot be removed
  • Wire mesh implants
  • Tissue expanders (e.g., breast)
  • Surgical staples, clips, or metallic sutures
  • Joint replacements (hip, knee, etc.)
  • Bone or joint pins, screws, nails, wires, plates, etc.
  • IUDs, diaphragms, or pessaries
  • Dentures or partial plates that cannot be removed
  • Tattoos or permanent makeup
  • Body piercing jewelry
  • Claustrophobia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University of California, San Francisco

San Francisco, California, United States, 94158

Actively Recruiting

Loading map...

Research Team

J

Joseph Chen, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here