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ENLITE PD: A Randomized Clinical Trial of Light Therapy for Impaired Sleep in Parkinson's Disease

  • NeuroNEXT NN110 ENLITE PD Investigators
  • Massachusetts General Hospital
  • University of Iowa
  • National Institutes of Health
  • University of Colorado Anschutz Medical Campus
  • Columbia University
  • Northwestern University
  • Vanderbilt University
  • Washington University St. Louis
  • University of Alabama at Birmingham
  • University of Cincinnati
  • Yale University
  • Beth Israel Deaconess Medical Center
  • University of Miami
  • University of Rochester
  • SUNY Upstate Medical University
  • University of Utah
  • Ohio State University
  • University of California at Irvine
  • Cornell University
  • University of Virginia
  • St. Joseph's Hospital and Medical Center, Phoenix
  • University of Pennsylvania
  • University of Pittsburgh
  • Wake Forest University
  • Icahn School of Medicine at Mount Sinai
  • University of Michigan, Ann Arbor
  • University of California at Davis

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Background: Light therapy (LT) in Parkinson's disease improves sleep. Specific LT parameters require further study, including optimal frequency. Objectives: We aimed to determine if once- or twice-daily bright white light therapy (BWLT) improves sleep. Secondary aims compared once-weekly BWLT to twice-daily dim red light therapy (DRLT) as controls, estimated effects on fatigue, and adherence. Methods: A 16-week, randomized, phase 2, sham-controlled, dose-selection trial to select the superior BWLT frequency based on change in Parkinson's Disease Sleep Scale-2 (PDSS-2), participant burden, and safety. Participants were randomized to 8 weeks of twice-daily BWLT, once-daily BWLT, once-weekly BWLT, or twice-daily DRLT. An improvement of ≥1.7 points in 8-week change of PDSS-2 by daily BWLT relative to either control warranted advancing to a phase 3 trial. Results: A total of 150 participants were randomized (mean [SD], 67 [8.6] years; 57 [38%] female; PDSS-2 17.1 [6.7]). Mean 8-week change from baseline in PDSS-2 score improved (twice-daily BWLT −2.6 [95% CI: −4.4, −0.7]; once-daily BWLT -1.5 [−3.3, 0.3]; once-weekly BWLT −0.4 [−2.2, 1.4]; twice-daily DRLT −1.8 [−3.6, 0.1]) but did not meet criteria for advancing. Mean 8-week change from baseline in Parkinson's Disease Fatigue Scale (PFS-16) score improved (twice-daily BWLT −6.4 [−9.8, −3.0]; once-daily BWLT −2.2 [−5.5, 1.1]; once-weekly BWLT −0.5 [−3.9, 2.8]; and twice-daily DRLT −3.8 [−7.3, −0.4]). Mean adherence to LT was 63%–86%. Conclusions: ENLITE-PD did not meet the criteria for advancing daily LT to a phase 3 trial. LT was safe and well-tolerated with good adherence. Once-weekly BWLT was a non-inferior control compared with twice-daily DRLT.

Original languageEnglish
Pages (from-to)2445-2456
Number of pages12
JournalMovement Disorders
Volume40
Issue number11
DOIs
StatePublished - Nov 2025

Keywords

  • Parkinson's
  • fatigue
  • light therapy
  • sleep
  • sleep disturbance

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