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Table 1 Study inclusion and exclusion criteria

From: The effects of bright light treatment on affective symptoms in people with dementia: a 24-week cluster randomized controlled trial

Participants were eligible if they:

Patients were not eligible if they:

- were ≥ 60 years and in long-term care (> 4 weeks)

- had dementia in accordance with DSM-5

- had either sleep/circadian rhythm disturbances, BPSD as identified by NPI-NH, or severely reduced ADL function

- provided written informed consent if the participant had capacity or, if not, a written proxy informed consent from a legally authorized representative

- were blind or might otherwise not benefit from light

- took part in another trial

- had a condition contra-indicated to the intervention

- had an advanced, severe medical disease/disorder and/or expected survival of less than 6 months, or other aspects that could interfere with participation

- were psychotic or had a severe mental disorder

  1. ADL Activities of Daily Living, BPSD Behavioral and Psychological Symptoms of Dementia, DSM-5 Diagnostic and Statistical Manual of Mental Disorders-5, NPI-NH Neuropsychiatric Inventory-Nursing Home Version