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Using a Wireless Controller to Deliver a Lighting Intervention to Persons With Dementia

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Mount Sinai Health System

Status

Completed

Conditions

Alzheimer's Disease

Treatments

Device: Control lighting intervention
Device: Active lighting intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05519137
STUDY-20-01772

Details and patient eligibility

About

To test the effect of a tailored lighting intervention controlled by the Readings At Desk (RAD) controller on sleep and mood in Alzheimer's disease participants.

Full description

Each participant will be enrolled for 22 weeks. Participants will be randomly assigned to receive either the active or control lighting condition. Each lighting condition will be 8 weeks in length. After a 4 week washout, each participant will crossover to the opposite condition. Assessments will be performed before and at the end of each lighting intervention.

Enrollment

14 patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of Alzheimer's disease with a Mini Mental Score Examination (MMSE) between 0 and 19
  • a score >5 on the PSQI.

Exclusion criteria

  • use of sleep medication

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

14 participants in 2 patient groups

Active lighting intervention then Control lighting condition
Active Comparator group
Description:
Each lighting condition will be 8 weeks in length. After a 4 week washout, each participant will crossover to the opposite condition.
Treatment:
Device: Active lighting intervention
Device: Control lighting intervention
Control lighting condition then Active light intervention
Active Comparator group
Description:
Each lighting condition will be 8 weeks in length. After a 4 week washout, each participant will crossover to the opposite condition.
Treatment:
Device: Active lighting intervention
Device: Control lighting intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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