Condition: Mild Cognitive Impairment · Sponsor: Icahn School of Medicine at Mount Sinai
Participants will randomly be placed into one of four groups and experience one of the four following conditions: (1) a placebo light that provides a 40 hertz (Hz) flicker (rhythmic light \[RL\]); (2) a placebo light with a random flicker (placebo condition for rhythmic light); (3) a light source that will stimulate the circadian system and provides a 40 Hz flicker (RL); or (4) a light source that will stimulate the circadian system and provides a random flicker (placebo condition for rhythmic light). Following a baseline week, participants will experience his/her assigned lighting condition for two hours in the morning for 8 weeks. After a 4-week washout period, a final round of assessments will be obtained. Study assessments (except for the Pittsburgh Sleep Quality Index and Montreal Cognitive Assessment) will be collected at the end of each week, for a total of 8 assessments.
This description comes directly from the study's public registry record.
Barbara Plitnick, BSN · 518-242-4603 · barbara.plitnick@mountsinai.org
Mariana Figueiro, PhD · 518-366-9306 · mariana.figueiro@mountsinai.org
Always discuss trial participation with your own doctor first.
| Light and Health Research Center | Menands, New York, United States | Recruiting |
| Icahn School of Medicine at Mount Sinai | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05016219