None listed
Conditions
Brief summary
In this project, we will use a new therapeutic lighting technology developed by our team at Queensland University of Technology, that can provide preferentially directed light spectrums to increase melanopsin activity thus may improve non-motor circadian/sleep behavior and motor symptoms in people with PD. Participants will be exposed to the light therapy at home every day for 30 minutes over 4 weeks and sleep and motor function will be assessed before, after 4 and 6 weeks of light intervention. We hypothesize that using light to preferentially activate melanopsin cells in the eye will help people with Parkinson’s disease sleep better. A better sleep will also positively impact on their movements such as balance, gait and tremor during the day.
Interventions
Supplemental light therapy: Arm 1: High melanopsin light Arm 2: Low melanopsin light The ‘high’ melanopsin state has a relatively increased spectral component around the peak sensitivity of the melanopsin photopigment. The ‘low’ melanopsin state has a relatively reduced spectral component in that range compared with the ‘high’ state. The melanopsin contrast between these states is approximately 25%. Each state’s total radiometric power is approximately 1.4W/m^2 (watts per square metre) and 2.8W/m^2 respectively, measured at 30cm. Of this, 0.445W/m^2 and 0.56W/m^2 respectively is acting on melanopsin photoreceptors, and both states have 0.808W/m^2 attributable to photometric luminance. Both states will not deliver more than the industry standard 10,000 lux at a 16cm viewing distance (e.g. approximately 5,000 lux). The participant will view the light for 30 minutes daily at home for 4 weeks. The participant will be instructed face to face by one of the research team members on the use of the light. We personalize the timing (morning or evening) of the daily (30min) light exposure based on a person’s chronotype to control for individual differences in activity and alertness in the morning and evening. Chronotypes will be determined with the Morningness Eveningness questionnaire. Actigraphy data provide an additional control measure to ensure adherence to the light intervention methodologies; that is, if the participant incorrectly uses the light, the actigraphy data will return lower light exposure when light box should have been used.
Sponsors
Study design
Eligibility
Inclusion criteria
• People with PD based on the unified Parkinson’s Disease Rating Scale (MDS-UPDRS) and Hoehn & Yahr staging (I-IV). • Healthy eyes with no anterior eye disease (i.e. lens opacities < grade 2 based on LOCS III) and no signs of retinal or optic nerve disease (diabetic retinopathy, glaucoma or age-related macular degeneration) based on ophthalmic examination (determined by an ophthalmologist, PI Feigl) • Living independently in the community and able to walk unaided
Exclusion criteria
• Inability to comply with study follow up • Participants having travelled across 2 or more time zones within 90 days before start of the study • Dementia based on MMSE (<24) and ACE (<82) assessments • Deep brain stimulation, other device assisted therapies (i.e. red light therapy) or CNS surgery • Any type of systemic disease or any medical condition (controlled or uncontrolled) other than PD that could be expected to significantly affect the health of a participant • A periodic limb movement disorder index (PLMI) > 15/hour in PSG • Significant sleep apnea (AHI apnoea-hypnoea index > 15 events/hour) and loss of REM atonia in PSG • Recent or recurrent history of musculoskeletal injury or surgery