N/A
N=191
Population Based Lighting Study on Older Adults
Lightning Strategies on Health · Circadian Rhythms Photoentrainment · Photoentrainment and Sleep · DLMO
Bottom Line
View on ClinicalTrials.gov: NCT05676086 ↗Enrolled (actual)
191
Serious AEs
0.0%
Results posted
May 2026
Primary outcome: Primary: Change in Pittsburgh Sleep Quality Index (PSQI) — 0; 0 Score change — p=0.14
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- indoor light intervention (Behavioral); no indoor light (Behavioral)
- Age
- Older Adult · 65+ yrs
- Sex
- All
- Sponsor
- Azienda Usl di Bologna
- Primary completion
- Feb 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Pittsburgh Sleep Quality Index (PSQI) |
0; 0 | 0.14 |
| SECONDARY Change in Mental and Physical Health (Euroqol 5D) |
0.00; 0.00 | — |
| SECONDARY Change in Circadian Rest-activity Measures - Interdaily Stability (IS) |
-0.01; -0.01 | — |
| SECONDARY Change in Circadian Rest-activity Measures - Intradaily Variability (IV) |
-0.01; -0.02 | — |
| SECONDARY Change in Circadian Rest-activity Measures - Relative Amplitude (RA) |
-0.01; 0.01 | — |
Summary
The ENLIGHTENme project aims at collecting evidence about the impact of outdoor and indoor lighting on human health and wellbeing through the development and testing of innovative solutions and policies that will also counteract health inequalities in European cities. In particular, through an open-online Urban Lighting and Health Atlas, ENLIGHTENme will collect and systematize existing data and good practices on urban lighting and will perform an accurate analysis on the correlations among health, wellbeing, lighting and socio-economic factors in three pilot cities: Bologna (Italy), Amsterdam (The Netherlands), and Tartu (Estonia).
Eligibility Criteria
Inclusion Criteria
- Living in the three selected cities within the target district chosen for the study
- Women and men
- Age 65 years or older
- Signing informed consent
Exclusion Criteria
- Lack of or inability to provide informed consent
- Lack of or inability to allow data collection over the course of the study
Data sourced from ClinicalTrials.gov (NCT05676086). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.