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Effect of Bright Light Treatment On Elders In a Long Term Care Environment

Not Applicable
Completed
Conditions
Behavioral Responses to Bright Light Therapy in Elders
Interventions
Other: exposure to bright light
Other: low luminosity red light
Registration Number
NCT01042587
Lead Sponsor
Milton S. Hershey Medical Center
Brief Summary

The investigators hypothesize that significant exposure to artificial morning bright light (approximately 200 lux of primarily blue light at eye level for thirty minutes daily) as compared to sham bright red light (placebo) will:

1. improve sleep quality

2. improve cognitive scores

3. improve depression scores

4. improve quality of life scores.

Detailed Description

Bright light therapy has been shown to improve depression and insomnia in multiple studies. These are common conditions among elders, particularly those residing in long term care environments. Bright light therapy has been inadequately studied in the geriatric population. We will show that a groups of twenty elders can simultaneous be exposed to bright light and that it will result in improvements in multiple realms of behavior and quality of life. Elders will be tested with a number of neuropsychological test batteries prior to exposure to bright light and again at the end of a four week exposure. Some subjects will have daytime and night time activity levels monitored with actigraphy. Cortisol and melatonin levels will be obtained prior to and at the end of the exposure period.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • residents in Masonic Villages, Elizabethtown, PA long term care
  • ability to give informed consent and complete the neuropsychological tests
Exclusion Criteria
  • blindness
  • severe illness expected to preclude the ability to complete treatment
  • moderate to severe dementia that precludes the ability to complete testing
  • light sensitivity making treatment to light therapy uncomfortable

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
bright lightexposure to bright lightBright light has been shown to entrain circadian rhythm so our treatment arm will use thirty minutes of early morning exposure to bright blue light for a four week period.
red lightlow luminosity red lightLow level red light is a weak entrainment stimulus of circadian rhythm. Elders in the control group will be exposed to low level red light as a placebo for thirty minutes daily for four weeks.
Primary Outcome Measures
NameTimeMethod
assessment of cognitive functioning using MicroCogonce prior to intervention, once near the end of intervention, once four weeks after intervention
Assessment of mood using the Geriatric Depression Scaleonce prior to intervention, once near the end of intervention, once four weeks after intervention
assessment of quality of life using the SF-36once prior to intervention, once near the end of intervention, once four weeks after intervention
assessment of sleep quality using the Pittsburgh Sleep Quality Indexonce prior to intervention, once near the end of intervention, once four weeks after intervention
assessment of mood using the Profile of Moods Surveyweekly throughout the duration of the study
assessment of sleep quality using the Epworth Sleepiness Scaleweekly throughout the duration of the study
day and nightime activity level (5 subjects per group only) using Actigraphytwo weeks prior to light exposure and the second two weeks during light exposure (continuous measurements)
Secondary Outcome Measures
NameTimeMethod
salivary melatonin levelsonce prior and near the end of light exposure period
salivary cortisol levelsonce prior and near the end of light exposure period

Trial Locations

Locations (1)

Masonic Villages

🇺🇸

Elizabethtown, Pennsylvania, United States

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