Lighting Intervention to Improve Sleep

Status Recruiting

Clinical Trial Summary

50 participants with Parkinson's disease will be recruited to complete actigraphy studies to assess sleep disturbances. For this, participants will wear an Actigraph for seven days. Thirty of these participants with sleep disturbance, will go on to receive a tailored lighting intervention (TLI) to assess the effect on sleep, fatigue, and circadian entrainment via urinary melatonin levels.

Clinical Trial Description

Participants will undergo one week of baseline data collection using the actigraph and light meter and one night of an overnight urine collection. At the completion of the baseline week, the lighting intervention will be installed in the participants home. Participants will be exposed to the lighting intervention for 2 hours each morning after awakening for 4 weeks. During the last week of the lighting, participants will be asked to wear the actigraph and light meter again for 7 days and collect one overnight urine sample. Participants will complete questionnaires before and after the intervention to further assess its effects. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05757414
Study type	Interventional
Source	Icahn School of Medicine at Mount Sinai
Contact	Maya Rawal
Phone	212-844-8373
Email	maya.rawal@mountsinai.org
Status	Recruiting
Phase	N/A
Start date	November 16, 2021
Completion date	March 2025

View Details

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