Clin2
NCT06245031Worth exploringEnrolling by invitation

Long-term follow-up of sensory stimulation for Alzheimer's

Alzheimer DiseaseCognitive ImpairmentMild Cognitive ImpairmentDementia, MildDementia ModerateDementia AlzheimersDementia of Alzheimer TypeAD

Part of Blood & lymphatic, Brain & nervous system, Cancer, Immune system & allergy, Mental health clinical trials.

This is a follow-up study for people who already completed the 12-month Hope Study (CA-0011). It tests long-term safety and effects of a gentle sensory stimulation device (light and sound) for Alzheimer's disease. You will continue using the device at home with a study partner.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
402 people
Ages
50 years to 92 years
Study type
Interventional

Who can take part

  • You must have completed the 12-month Hope Study (CA-0011) for Alzheimer's disease.
  • You need a study partner — a family member or friend who can help with visits.
  • You cannot be living in a full-time nursing home (assisted living is permitted).
  • You cannot be taking certain medications during the study: monoclonal antibodies for Alzheimer's, memantine (Namenda or Namzaric), or nootropic drugs (except stable doses of donepezil/rivastigmine).
  • If you can become pregnant, you must agree to use effective birth control.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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