search
Back to results

Individually Tailored Lighting System to Improve Sleep in Older Adults

Primary Purpose

Sleep Disturbances

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Blue light
Red light
Sponsored by
Rensselaer Polytechnic Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Disturbances focused on measuring light, circadian rhythms, dim light melatonin onset, sleep

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • age 65 or older
  • cognitively capable
  • able to respond to study staff verbally and in English
  • score greater than 6 using the Pittsburgh Sleepiness Quality Index
  • suffer from insomnia
  • suffer from excessive daytime sleepiness

Exclusion Criteria:

  • Severe sleep apnea
  • Severe restless leg syndrome (RLS)
  • Significant cognitive impairment
  • History of severe photosensitivity dermatitis

Sites / Locations

  • Rensselaer Polytechnic Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Blue light

Red light

Arm Description

The study protocol consisted of two 8-week intervention/control periods in which each participant wore either the intervention (blue light) or control (red light) mask every night, with the order of presentation of the two conditions randomized by the study's biostatistician. A light mask housing two blue Light Emitting Diodes (LED) arrays delivered a train of blue or red light pulses of 2 second duration that were presented every 30 s for no longer than 2 hr, resulting in a maximum total of approximately 240 pulses per night. the blue light mask was worn nightly for 8 weeks. There will be a two week washout period between each intervention

The study protocol consisted of two 8-week intervention/control periods in which each participant wore either the intervention (blue light) or control (red light) mask every night, with the order of presentation of the two conditions randomized by the study's biostatistician. A light mask housing two red Light Emitting Diodes (LED) arrays delivered a train of blue or red light pulses of 2 second duration that were presented every 30 s for no longer than 2 hr, resulting in a maximum total of approximately 240 pulses per night. the red light mask was worn nightly for 8 weeks, with a two week washout period between each intervention

Outcomes

Primary Outcome Measures

Sleep Disturbance
Pittsburgh Sleep Quality Index. Score range 0 - 21. A score over 5 is indicative of sleep disturbance. Change in score from baseline to intervention is reported. A larger difference indicates a better outcome.
Total Sleep Time
The change in total amount of minutes spent sleeping at night from baseline week to the last week of intervention. A higher number is an improved outcome
Sleep Efficiency
The change in sleep efficiency from baseline to last week of intervention. A higher number is a better outcome. Sleep efficiency is the percentage of time spent in bed sleeping. Scored total sleep time divided by interval duration minus total invalid time (sleep/wake) of the given rest interval multiplied by 100. This data was collected using actigraphy data.
Sleep Start Time
Change in sleep start time, in minutes, from baseline week to the last week of intervention. A higher number is a better outcome. Based on actigraph data

Secondary Outcome Measures

Full Information

First Posted
May 9, 2013
Last Updated
January 7, 2019
Sponsor
Rensselaer Polytechnic Institute
Collaborators
University of North Carolina
search

1. Study Identification

Unique Protocol Identification Number
NCT01855126
Brief Title
Individually Tailored Lighting System to Improve Sleep in Older Adults
Official Title
Individually Tailored Lighting System to Improve Sleep in Older Adults
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
April 2017 (Actual)
Study Completion Date
April 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rensselaer Polytechnic Institute
Collaborators
University of North Carolina

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In conjunction with investigators at the Cecil G. Sheps Center for Health Services Research, University of North Carolina (UNC) at Chapel Hill, we propose to develop and evaluate a low-cost, minimally obtrusive device that delivers individualized light therapy to adults with early-awakening insomnia - the most common sleep disturbance in older adults, and a significant problem because of its relationship to daytime sleepiness, use of potentially hazardous sleep medication, and reduced quality of life. The proposed device will measure light/dark exposure data over 24 hours, estimate optimum timing for light delivery, and deliver an individualized light dosage while subjects are asleep. Light applied through closed eyelids in the early part of the night will delay the dim light melatonin onset, a marker of the circadian clock, and help those with early sleep onset to fall asleep later
Detailed Description
We will recruit 50 subjects who report going to bed early and desiring later bedtimes and will ask them to wear an active and an inactive light mask for 8 consecutive weeks each. A 2-week washout period between active and inactive conditions will be applied. Outcome measures will be collected periodically throughout the 8 weeks. Baseline (no intervention) will be collected prior to the active and inactive lighting interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Disturbances
Keywords
light, circadian rhythms, dim light melatonin onset, sleep

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Enrolled participants will be randomized to receive either the active intervention or placebo intervention and then crossed over to receive the opposite intervention. The study consisted of two intervention periods of 8 weeks separated by a two week washout period.
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Blue light
Arm Type
Experimental
Arm Description
The study protocol consisted of two 8-week intervention/control periods in which each participant wore either the intervention (blue light) or control (red light) mask every night, with the order of presentation of the two conditions randomized by the study's biostatistician. A light mask housing two blue Light Emitting Diodes (LED) arrays delivered a train of blue or red light pulses of 2 second duration that were presented every 30 s for no longer than 2 hr, resulting in a maximum total of approximately 240 pulses per night. the blue light mask was worn nightly for 8 weeks. There will be a two week washout period between each intervention
Arm Title
Red light
Arm Type
Placebo Comparator
Arm Description
The study protocol consisted of two 8-week intervention/control periods in which each participant wore either the intervention (blue light) or control (red light) mask every night, with the order of presentation of the two conditions randomized by the study's biostatistician. A light mask housing two red Light Emitting Diodes (LED) arrays delivered a train of blue or red light pulses of 2 second duration that were presented every 30 s for no longer than 2 hr, resulting in a maximum total of approximately 240 pulses per night. the red light mask was worn nightly for 8 weeks, with a two week washout period between each intervention
Intervention Type
Other
Intervention Name(s)
Blue light
Intervention Description
After a two week baseline collection period, half of the subjects will initially be given light masks that deliver blue light through the closed eyelids, while subjects are sleeping. The light mask will always be turned on 120 min before estimated core body temperature minimum (CBTmin); it is expected that blue light exposure will delay the timing of the CBTmin.
Intervention Type
Other
Intervention Name(s)
Red light
Intervention Description
After a two week baseline collection period, half of the subjects will initially be given light masks that deliver red light through the closed eyelids, while subjects are sleeping. The light mask will always be turned on 120 min before estimated core body temperature minimum (CBTmin); it is expected that red light exposure will have no effect on the timing of the CBTmin.
Primary Outcome Measure Information:
Title
Sleep Disturbance
Description
Pittsburgh Sleep Quality Index. Score range 0 - 21. A score over 5 is indicative of sleep disturbance. Change in score from baseline to intervention is reported. A larger difference indicates a better outcome.
Time Frame
Baseline (week 0) and week 8 of lighting intervention
Title
Total Sleep Time
Description
The change in total amount of minutes spent sleeping at night from baseline week to the last week of intervention. A higher number is an improved outcome
Time Frame
baseline week (week 0) and the last week of intervention (week 8)
Title
Sleep Efficiency
Description
The change in sleep efficiency from baseline to last week of intervention. A higher number is a better outcome. Sleep efficiency is the percentage of time spent in bed sleeping. Scored total sleep time divided by interval duration minus total invalid time (sleep/wake) of the given rest interval multiplied by 100. This data was collected using actigraphy data.
Time Frame
baseline week (week 0) and the last week of intervention (week 8)
Title
Sleep Start Time
Description
Change in sleep start time, in minutes, from baseline week to the last week of intervention. A higher number is a better outcome. Based on actigraph data
Time Frame
baseline week (week 0) and the last week of intervention (week 8)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: age 65 or older cognitively capable able to respond to study staff verbally and in English score greater than 6 using the Pittsburgh Sleepiness Quality Index suffer from insomnia suffer from excessive daytime sleepiness Exclusion Criteria: Severe sleep apnea Severe restless leg syndrome (RLS) Significant cognitive impairment History of severe photosensitivity dermatitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mariana G Figueiro, PhD
Organizational Affiliation
Rensselaer Polytechnic Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rensselaer Polytechnic Institute
City
Troy
State/Province
New York
ZIP/Postal Code
12180
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25506253
Citation
Figueiro MG, Plitnick B, Rea MS. Pulsing blue light through closed eyelids: effects on acute melatonin suppression and phase shifting of dim light melatonin onset. Nat Sci Sleep. 2014 Dec 2;6:149-56. doi: 10.2147/NSS.S73856. eCollection 2014.
Results Reference
background
PubMed Identifier
24124400
Citation
Figueiro MG, Bierman A, Rea MS. A train of blue light pulses delivered through closed eyelids suppresses melatonin and phase shifts the human circadian system. Nat Sci Sleep. 2013 Oct 4;5:133-41. doi: 10.2147/NSS.S52203. eCollection 2013.
Results Reference
background

Learn more about this trial

Individually Tailored Lighting System to Improve Sleep in Older Adults

We'll reach out to this number within 24 hrs