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AzTrials

Sleep QualityLISNCT06687304

Light in Healthcare Environment (Ljus i sjukhusmiljö)

A study testing Light enhancement in people with Sleep Quality and Well-being, run by Lund University at 3 sites in Sweden.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to learn if light can enhance the feeling of well-being and sleep quality in Radiographers. It will also find out if there is an optimal recipe for light. Read more about this study

Who is it for?
Ages 21 years and olderHealthy volunteers can take part
Conditions the study is for
Sleep Quality, Well-being, Melatonin
What is being tested?
Light enhancement
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
18 participants
Where
3 sitesSweden
Study dates
15 Nov 2024to 31 Mar 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Radiographer

Who cannot join

  • -

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Pether Jildenstal, PhD contact

0046462220000

pether.jildenstal@med.lu.se

Sweden3 sites, 3 recruiting
  • Skånes universitetssjukhus Lund

    Lund, Skåne County, 22242

    Camilla Viseu, +46 705425698, camilla.viseu@med.lu.se

    Recruiting
  • Skånes universitetssjukhus

    Malmö, Skåne County, 21428

    Camilla Viseu, +46 705425698, camilla.viseu@med.lu.se

    Recruiting
  • Lasarettet Trelleborg

    Trelleborg, Skåne County, 23155

    Camilla Viseu, +46 705425698, camilla.viseu@med.lu.se

    Recruiting

Other trials in Sweden

About this study

Official title: Benefits of Light in the Radiographic Environment

The goal of this clinical trial is to learn if light can enhance the feeling of well-being and sleep quality in Radiographers. It will also find out if there is an optimal recipe for light. The main questions it aims to answer are:

  • Will alertness, energy levels, and sleep quality increase in radiographers when the lighting is differed?
  • What light recipe is the most beneficial for the personnel? Researchers will compare no enhanced light environment to different enhanced light environment to see if the enhanced light is beneficial for radiographers.

Participants will:

  • Will work in an enhanced light environment or a non-enhanced light environment
  • Answer surveys
  • Take saliva sample
Read the detailed description

The aim of this study is to examine the impact of different daylight lighting conditions in the radiographer's workplace environment. Will alertness, energy levels, well-being, and sleep quality increase in the personnel at the radiology department when the lighting is differed? Which light recipe is the most beneficial for the personnel at the radiology department? Method Design: In order to ascertain the light level that yields the desired effect, an quasi-experimental study design will be employed to identify the optimal light recipe with the appropriate light intensity. A crossover design is intended for implementation. This design approach offers the advantage of having each participant serve as their own control, thereby minimizing the potential impact of inter-group differences on the results. Furthermore, it enhances statistical efficiency, even with a reduced number of study participants (Lim \& In, 2021).

Context/recruitment: Recruitments of personnel from various radiology departments at Skåne University Hospital (SUS) in Lund are planned to be conducted. A total of 18 the personnel at the radiology department will be included during the darker months of the year. At 10 to 20 workstations, a floor lamp equipped with an adjusted light prescription will be installed. Participants will be assigned to conditions in which the lamp will either be activated with the specified light recipe or remain turned off. After a duration of two weeks, the conditions will be reversed for an additional two-week period. This process will be repeated using four different light recipes to evaluate their effects on the energy levels, activity, and sleep quality of the staff. The objective is to gather insights from each season that can be implemented in the subsequent winter to determine the optimal light level.

Data collection: Subjective Measurement Methods - Staff Surveys

General Survey Participants will be asked questions regarding their typical age and gender. Additionally, a modified version of the Morningness-Eveningness Questionnaire (MEQ) will be utilized to determine each individual;s chronotype (Adan \& Almirall, 1991). A Swedish translation of this questionnaire has proven effective in assessing chronotype and is appropriate for use when a shorter assessment tool is needed (Danielsson et al., 2019).

Karolinska Sleepiness Scale (KSS) To assess the level of alertness and energy among study participants, the KSS will be utilized. This scale employs a 9-point Likert format to evaluate perceived fatigue and energy levels (Åkerstedt \& Gillberg, 1990). The KSS has been utilized in various research studies to examine the impact of lighting conditions on perceived alertness.

Patient-Reported Outcomes Information System Short Form Sleep Disturbance 8a(PROMIS) The Patient-Reported Outcomes Measurement Information System (PROMIS) is an assessment tool designed to measure self-reported sleep disturbances, including sleep quality, difficulty falling asleep, and staying asleep. It consists of 8 items rated by patients to evaluate the frequency and severity of sleep issues, supporting clinical insights into sleep-related health impacts.

Furthermore, participants \& well-being will be quantified utilizing the WHO-5 Well-Being Index.

Objective Measurement Methods: Sleep Data via Activity Bands - Actiwatch

The employment of activity monitors allows for the objective measurement of sleep. The actigraphy device is worn on the non-dominant wrist and is non-invasive (Weiss et al., 2010). It continuously tracks the participant's movements and records sleep parameters including duration and quality. These measurements can subsequently be analyzed (Ancoli-Israel et al., 2015). Due to the impracticality of wearing these wristbands during working hours, participants will attach them to their clothing at work and wear them on their wrist after work hours.

Additionally, saliva samples will be collected to measure cortisol and melatonin levels in the study participants. Cortisol secretion is stimulated by dawn light or, in winter, often by office lighting. This secretion level provides an objective parameter for assessing activation. Conversely, melatonin secretion is suppressed by the light of dawn, and the extent of this inhibition serves as an indicator of the lights effectiveness.

Being tested
Light enhancement
Keywords
Light, Radiography, Light environment, Circadian rhythm, Personnel at radiology departments
Medical subject headings
Sleep Initiation and Maintenance Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Light enhancementDevice

    Also called Lamp, Light recipe, Dynamic lighting

    Light recipe that mimics the varying daylight of the day

Study groups in NCT06687304
Study groupRoleWhat they receive
Enhanced light environmentActive comparatorNot described
Receives: Device: Light enhancement
Non-enhanced light environmentNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Karolinska Sleepiness Scale (KSS)

    To assess the subjective level of sleepiness at a particular time during the day

    Measured: Measurements will be taken three times daily over a period of 16 to 20 weeks, depending on the start date of the inclusion phase, for each period.

  2. WHO-5 Well-Being Index

    To assess the level of well-being, the WHO-5 Well-Being Index is used. It's a brief, self-reported measure of current mental well-being, consisting of five questions that assess positive mood, vitality, and general interest over the past two weeks.

    Measured: Measurements will be taken at the start and then second Friday in each two-week period over the 16 to 20 weeks (depending on when the inclusion phase can begin) during which inclusion occurs for each season.

  3. PROMIS

    Patient-Reported Outcomes Measurement Information System (PROMIS) is a standardized, self-reported questionnaire designed to measure an individual's perception of their sleep quality, specifically addressing issues like difficulty falling asleep, staying asleep, and feelings of restlessness. It consists of 8 items that gauge the severity of sleep disturbances over the past seven days.

    Measured: Measurements will be taken at the start and then every Friday in each two-week period over the 16 to 20 weeks (depending on when the inclusion phase can begin) during which inclusion occurs for each season.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Nov 2024
  2. Study start15 Nov 2024
  3. Primary completion31 Mar 2027 (estimated)
  4. Study completion31 Mar 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Non-randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
18 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06687304
Sponsor's protocol ID
2024-04436-02
Acronym
LIS
Status last verified
Nov 2025
First submitted
4 Nov 2024
Last updated
2 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Weiss AR, Johnson NL, Berger NA, Redline S. Validity of activity-based devices to estimate sleep. J Clin Sleep Med. 2010 Aug 15;6(4):336-42.

    PubMed 20726281
  • Ancoli-Israel S, Martin JL, Blackwell T, Buenaver L, Liu L, Meltzer LJ, Sadeh A, Spira AP, Taylor DJ. The SBSM Guide to Actigraphy Monitoring: Clinical and Research Applications. Behav Sleep Med. 2015;13 Suppl 1:S4-S38. doi: 10.1080/15402002.2015.1046356. No abstract available.

    PubMed 26273913

Questions about this trial

What is this clinical trial studying?

A study testing Light enhancement in people with Sleep Quality and Well-being, run by Lund University at 3 sites in Sweden.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 2 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Pether Jildenstal, PhD (0046462220000, pether.jildenstal@med.lu.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Karolinska Sleepiness Scale (KSS) (time frame: Measurements will be taken three times daily over a period of 16 to 20 weeks, depending on the start date of the inclusion phase, for each period.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06687304, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Dec 2025.

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