NCT07206251

Brief Summary

To enable the Netherlands to reach the 2030 carbon emission goals, older homes need to be renovated to become more energy-efficient and comfortable. This project aims to provide shallow renovations of window films. These shallow renovations can be completed in 1-2 days and cost significantly less than a deep renovation. The study aims investigate how such window films can affect humans (low-e film and thermochromatic) if applicated in real life.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
41

participants targeted

Target at P50-P75 for not_applicable healthy

Timeline
Completed

Started Jul 2024

Shorter than P25 for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 26, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 29, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 29, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

March 20, 2025

Completed
7 months until next milestone

First Posted

Study publicly available on registry

October 3, 2025

Completed
Last Updated

January 16, 2026

Status Verified

January 1, 2026

Enrollment Period

3 months

First QC Date

March 20, 2025

Last Update Submit

January 15, 2026

Conditions

Keywords

Window FoilThermoregulationThermal PerceptionDaylightSalivaCognition

Outcome Measures

Primary Outcomes (1)

  • Cognitive Performance Scores

    Participants completed 2 cognitive battery tests (Creyos) during each test day at 2 different timepoints; one early afternoon, the other late afternon.

    2 x in 5 hours test session both test days

Secondary Outcomes (2)

  • Skin Temperature

    every 1 min it is collected automatically over 5 hours test day and 2 test days

  • Visual Scale

    every 30mins to 1 hour over 5 hours test day and 2 sessions in total

Study Arms (2)

Regular Windowed room (no foil added)

NO INTERVENTION

Regular Windowed room (no foil added)

Foiled Windowed room (foil added)

EXPERIMENTAL

Foiled Windowed room (foil added)

Behavioral: Foiled Windowed room (foil added)

Interventions

Foiled Windowed room (foil added)

Foiled Windowed room (foil added)

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Generally Healthy Adult
  • Ages between 18-40 years old
  • Normal or correct vision (with use of glasses or contact lenses)
  • Full vision
  • Both males or females

You may not qualify if:

  • No Raynaud's syndrome
  • No metabolic or cardiovascular diseases
  • No ADHD or cognitive disorders
  • No night shift work
  • No colour blindness

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Vertigo - TU/e

Eindhoven, 5612 AV, Netherlands

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 20, 2025

First Posted

October 3, 2025

Study Start

July 26, 2024

Primary Completion

October 29, 2024

Study Completion

October 29, 2024

Last Updated

January 16, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Study is conducted by the researchers who will also process and analyse the data set anonymoously.

Locations