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Pilot Study to Evaluate Feasibility of Sensory Stimulation With Gamma Frequency Entrainment

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Despite the huge healthcare and economic impact of AD, there is still no disease modifying therapeutics available. In fact, the available therapeutics show low efficacy at best in the treatment of cognitive impairment in dementia. Development of a non-invasive medical device that is effective in slowing cognitive impairment is not only revolutionary but also possibly cost- effective. In this study, participants will come to MIT for a 1-day visit and the investigators will evaluate the effects of GENUS in cognitively normal, healthy adults. Investigators will use Electroencephalogram (EEG), Magnetoencephalography (MEG), magnetic resonance imaging (MRI), neuropsychological testing, and blood sampling in subsets of participants to evaluate for biological effects and safety of GENUS stimulation.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: t
View:

• Have adequate visual and auditory acuity for visual and auditory stimulation to allow for neuropsychological testing.

• Be able to comply with neuropsychological testing and other study procedures in opinion of site PI.

Locations
United States
Massachusetts
MIT
RECRUITING
Cambridge
Contact Information
Primary
gamma wave
gamma.wave@mit.edu
617-258-7723
Backup
Ana Trisini Lipsanopoulos, BS
anat13@mit.edu
617-258-7723
Time Frame
Start Date: 2018-02-20
Estimated Completion Date: 2027-01-30
Participants
Target number of participants: 150
Treatments
Experimental: Cognitively normal adults
Cognitively normal, healthy adults aged 18 - 100
Related Therapeutic Areas
Sponsors
Leads: Massachusetts Institute of Technology

This content was sourced from clinicaltrials.gov