Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
Healthy Volunteers
ID06687304

Benefits of Light in the Radiographic Environment to Improve Sleep and Well-being

Led by Lund University · Updated on 2025-12-02

18

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

Sponsors

L

Lund University

Lead Sponsor

A

AFA Insurance

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating whether different lighting conditions can improve alertness, energy, well-being, and sleep quality among radiographers working in a radiology department. The study aims to identify the best light setting, or "light recipe," that benefits staff the most by comparing standard lighting to enhanced lighting environments. This research uses a quasi-experimental crossover design, allowing each participant to experience both lighting conditions for accurate comparison. Participants will work in either an enhanced light environment, where a floor lamp mimics natural daylight, or a non-enhanced light environment with the lamp turned off. These conditions will each last two weeks before switching, and this cycle will repeat across four different light recipes. The study will take place during darker months and involve 18 radiology staff members at up to 20 workstations. Throughout the study, participants will complete surveys about their sleep, energy, and well-being, including the Karolinska Sleepiness Scale, PROMIS Sleep Disturbance, and WHO-5 Well-Being Index. They will also wear activity bands to track sleep objectively outside work hours and provide saliva samples to measure cortisol and melatonin levels. Measurements will be taken regularly over 16 to 20 weeks, depending on the inclusion timing. This detailed monitoring helps assess how lighting affects staff health and performance.

CONDITIONS

Brief Title

Light in Healthcare Environment (Ljus i sjukhusmiljö)

Who Can Participate

Age: 21Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Radiographer
  • Age 21 years or older
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - 16 to 20 weeks

Participants experience different lighting conditions at their workstations to evaluate the impact on alertness, energy, well-being, and sleep quality. The lighting conditions alternate between enhanced light recipes and non-enhanced light environments in a crossover design.

Multiple visits depending on assessment schedule during work periods

Monitoring

Duration - Concurrent with Implementation stage, over 16 to 20 weeks

Participants complete surveys and wear activity monitors to assess sleep quality, alertness, and well-being throughout the study periods under varying light conditions.

Surveys taken up to three times daily and weekly assessments during the study

Trial Site Locations

Total: 3 locations

1

Skånes universitetssjukhus Lund

Lund, Skåne County, Sweden, 22242

Actively Recruiting

2

Skånes universitetssjukhus

Malmö, Skåne County, Sweden, 21428

Actively Recruiting

3

Lasarettet Trelleborg

Trelleborg, Skåne County, Sweden, 23155

Actively Recruiting

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Research Team

P

Pether Jildenstal, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

CROSSOVER

Primary Purpose

PREVENTION

Number of Arms

2

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