Official Title
Impact of Everyday Light Exposure Patterns on Metabolic, Cardiovascular, and Psychological Health in Younger and Older Adults
Brief Summary

The aim of the present study is to characterize everyday light conditions of younger andolder adults and to consider them in relation to cardiovascular, metabolic andpsychological health. An ambulatory assessment approach will be used over 12 days,measuring physiological parameters and daily thoughts, behaviors and experiences ofdifferent age groups using wearable technologies (e.g., light sensors, activity trackers,continuous glucose monitors) and smartphone-based self-reports (e.g., mood, vitality).At the beginning of the study, the degeneration of the lens and retina of theparticipants is objectively quantified by ophthalmologists. On the last two days,participants will spend one working day in dim light and another in bright light inrandomized order under the same measurement protocol as before in order to experimentallyassess their sensitivity to light and its health effects.

Detailed Description

This study is designed as an observatory field study of characterizing younger and older
adults' everyday life in terms of light exposure patterns as well as cardiovascular,
metabolic and psychological health parameters over 10 days continuously through wearables
and smartphone-based self-reports (ambulatory assessment period). On the first day of
data collection, each participant will undergo an extensive eye examination at the
Institute of Ophthalmology, particularly an Optical Coherence Tomography (OCT) scan will
conducted and by means of a macular pigment reflectometer the difference between the
light entering and leaving the eye across the visual spectrum will be determined as a
marker of lense yellowing. Thereafter, participants start wearing the wearable sensors
(continuous glucose monitors, light loggers worn as a necklace) and instructions on how
to complete the smartphone-based self-report forms are provided. Participants are asked
to take pictures of every food or drink (except of water) and upload these pictures
through the m-Path app, these photos will be later linked to the continuous glucose
monitor data. Data will be collected from the first evening onwards (ca. 18:00 h). After
the ambulatory assessment period under free-living conditions, participants will spend
the 11th and 12th day in a controlled office room environment from 08:30 to 17:00 h. In a
randomized cross-over design, the 11th and 12th day will be spent in either bright (1250
lux) or dim office lighting (10 lux). On these days, participants will continue to wear
the wearables and complete the expanded smartphone-based self-reports mostly similar to
the 10-day ambulatory assessment period. Between day 11 and 12, participants will leave
controlled conditions from 17:00 h on day 11 to 08:30 h on day 12. On day 11 and 12,
participants will receive a standardized fluid meals for breakfast and lunch, and are
otherwise instructed to avoid any food, caloric or caffeinated beverages between 08:30
and 17:00 h. On these two days, skin temperature sensors will be placed on four different
skin regions, and blood pressure will be manually measured at regular intervals between
08:30 h and 17:00 h. After removing all wearables on day 12, the study ends at 17:30 h.
Over these 12 days of data collection, participants will be asked to keep their bedtimes
at home as consistent as possible between days, and on day 11 and 12 they will be
instructed to come to the office facilities fasted without any caloric intake after 22:00
h on the previous evening of day 10 and 11, respectively.

The two comparative groups formed in this study consist of 30 younger adults (18-35
years) and 30 older adults (60-80 years), both females and males will be included, and
the aim is to match both groups with respect to sex (i.e. ideally 15 women and 15 men per
group). The age contrast in the two groups is chosen, as substantial differences in
degeneration of the lenses and retina within the eye can be expected.

For the sample size calculation of n = 30 per group, we refer to Zauner et al. (Zauner et
al., 2023), who created a procedure to calculate statistical power and required sample
size for wearable light-logging data. For most light-logging metrics, their approach
shows that for strong differences in light exposure patterns (i.e., winter vs. summer)
even smaller samples are sufficient (n = 3-24). We do not expect that differences between
age groups are that strong as seasonal differences. However, we are confident that
effects of about d = 0.7 could be detected with our design (n = 30 per group).
Considering some drop-out, we anticipate that we will have to enroll 70 participants in
total.

With the primary hypothesis of this study being that younger and older individuals differ
in their light exposure patterns in everyday life, the two main explorative goals of the
AgeLight study are to:

- characterize light exposure patterns in younger and older adults and their link to
cardiovascular, metabolic, and psychological health

- identify determining factors of an individual's sensitivity to light and its health
effects (such as degeneration of the lens and retina)

Enrolling by invitation
Healthy Male and Female Subjects
Healthy Elderly

Other: 10-day ambulatory assessment in everyday life combined with two laboratory office days

Participants undergo a 10-day ambulatory assessment period wearing a continuous glucose
monitor and a light logger as a necklace as well as completing short questionnaires
through a smartphone app at regular intervals every day. On the first day, participants
also undergo an extensive eye examination. Day 11 and 12 are spent in either dim or
bright office lighting in randomized order.

Eligibility Criteria

Inclusion Criteria:

- Age: 18-35 or 60-80 years old

- Voluntary participation, signed consent form

- Owns an Android or iOS Smartphone compatible with the m-Path App

- Generally healthy (self-reported)

- Non-smoker for at least 12 months (self-reported)

Exclusion Criteria:

- Pregnancy (for female participants) (self-reported)

- Night-shift worker

- Eye diseases (e.g. glaucoma, age-related macular degeneration, diabetic retinopathy
conditions after retinal detachment / retinal blood vessel occlusions)

- Pseudophakic eyes

- Psychological disorders: insomnia, depression, bipolar disorder and generalized
anxiety disorder

- Wearing specially-filtered glasses

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 80 Years
Countries
Germany
Locations

University hospital at RWTH Aachen
Aachen, Germany

Jan-Frieder Harmsen, PhD, Principal Investigator
RWTH Aachen University

RWTH Aachen University
NCT Number
Keywords
Spectral diet
ambulatory assessment
daylight
m-path
eye degeneration
lense yellowing
Continuous glucose monitoring
healthy aging
light sensitivity
melanopic EDI