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Light Therapy in Parkinson's Disease

Not Applicable
Completed
Conditions
Parkinson's Disease
Interventions
Device: Placebo light therapy
Registration Number
NCT02072642
Lead Sponsor
University Hospital, Strasbourg, France
Brief Summary

Parkinson's disease, a degenerative disorder of the dopaminergic system, combines motor symptoms but also non-motor, such as depression, sleep disorders and circadian rhythms and impaired cognitive functions. Difficulties in balancing the dopaminergic treatment of these patients emphasizes the need to find effective adjuvant therapies. Light therapy (LT) represents one such innovative therapeutic approach. Although light has an obvious to visual pathways within the brain, today it is known to additionally exert non-visual effects throughout the body. Recently our team has shown that non-visual, non-circadian light plays a major role in the regulation of sleep, as well as cognitive brain function in general. The retina, the primary conduit for the transmission of light information is weakened or thinned in Parkinson's patients. The dopamine system is known to enhance the processing of light information and intraocular injection of L-dopa in animal models of Parkinson's disease, can reverse associated motor symptoms. This allows for the possibility that LT would strengthen the dopaminergic tone in the central nervous system. However, to this date its effectiveness for alleviating Parkinson's symptoms has only been suggested by two studies, both poorly controlled. Thus, through the convergence of basic and clinical data, a study examining the effect of LT directly in people Parkinson's disease symptoms, whilst controlling for the effects on sleep, circadian system, mood, and cognitive functioning, is of extreme importance. With this information our hope is to determine if these polymorphisms allow for a predictive model of response to LT treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
44
Inclusion Criteria
  • Idiopathic Parkison's Disease, low or moderately severe
  • Hoehn&Yahr <4
  • 4 to < 15 years of evolution路
  • Between 45-75 years old
  • Absence of dementia : MMSE > 23路
  • No severe depression
  • Stable medication levels during the 5 weeks before inclusion
Exclusion Criteria
  • Secondary or severe Parkinson's disease
  • Ocular pathologies (i.e. retinopathy)
  • Photosensitive medication
  • Antidepressant treatment路
  • Major depression syndrome
  • MMSE < 23
  • Circadian rhythm problems
  • Sleep apnea syndrome
  • Manifested or acute psychiatric comorbidities
  • Pregnant women

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Placebo light therapy (70 lux)Placebo light therapyPlacebo light therapy
Primary Outcome Measures
NameTimeMethod
Global score :Unified Parkinson's Disease Rating Scale (UPDRS) I II III5 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Hospital, Strasbourg, france

馃嚝馃嚪

Strasbourg, France

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