NCT06451952 · RECRUITING

Virtual Darkness Theraphy for Agitation in Dementia

This trial is testing whether blocking blue-wavelength light in the evening and overnight — called virtual darkness therapy — reduces agitation in people with dementia who are hospitalized. Patients wear amber-tinted glasses or are placed in blue-light-filtered environments from 7pm to 8am. Researchers measure agitation levels before and after 14 days. This is a Phase NA trial, meaning it is exploratory and feasibility-focused, not yet a large-scale proven treatment.

You may qualify if

  • Patients admitted to NKS Olaviken gerontopsychiatric hospital
  • Diagnosis of dementia, all stages and etiologies,
  • ≥50 years
  • both genders
  • Clinically significant agitation (CMAI ≥45)

You're excluded if

  • Total blindness/diminished bilateral red reflex.
  • Use of melatonin
  • Clinically significant pain (MOBID-2≥3)

The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.

Eligibility criteria as of 2025-04-11

View full record on ClinicalTrials.gov

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