Night Work Hours Reduction Trial
WHRedu
Trial of Reduced Working Hours Among Regular Night Shift Workers in Public Health and Social Care
1 other identifier
interventional
200
1 country
3
Brief Summary
The primary aim of this study is to investigate the effects of reducing weekly working hours among employees working night shifts regularly from 38 hours 15 minutes to 36 hours on payroll-based, objective working-hour characteristics, sickness absence, and workforce retention. The secondary aim is to investigate experiences of promoting and hindering factors related to the working-hour reduction, its implementation process, and perceived benefits and challenges. The working-hour reduction will be implemented in three Finnish wellbeing services counties with different starting dates, the first being in late September 2026 and the latest in early 2027. The working-hour reduction has been agreed upon by the parties to the collective agreement for Finnish public social and health care. Thus, intervention is a so-called natural experiment in a real-life setting. The effects of the intervention will be evaluated using a quasi-experimental design with staggered, non-randomized implementation across participating counties. Administrative, payroll-based, employer-owned working-hour data, including records of sickness absences without any medical or health information and other absences (including unpaid, education, and childcare), will be used to compare changes before and during the intervention among work units participating in the working-hour reduction. The investigation will also utilize matched work units that do not participate in the reduction (i.e., intervention) as control units (i.e., continuing standard working-hour arrangements).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2026
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 17, 2026
CompletedFirst Posted
Study publicly available on registry
September 30, 2026
CompletedStudy Start
First participant enrolled
September 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2028
September 30, 2026
September 1, 2026
1.4 years
September 17, 2026
September 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Sickness Absence Rate
Percentage of working time lost due to sickness absence, derived from administrative, payroll-based employer records. No medical or diagnostic information will be collected.
From enrollment to the end of treatment at 66 weeks.
Employee Turnover
Termination of employment during the follow-up period, derived from employment records.
From enrollment to the end of treatment at 66 weeks.
Retention of Employees Performing Night Work
Proportion of employees performing regular night work who remain employed and performing night shifts during the follow-up period.
From enrollment to the end of treatment at 66 weeks.
Total Weekly Working Hours
Average number of paid working hours per week, derived from administrative, payroll-based working-hour records.
From enrollment to the end of treatment at 66 weeks.
Number of Morning, Day, Evening, and Night Shifts
Number or rate of shifts worked during each scheduling period, categorized according to shift type (morning, day, evening, and night) using employer payroll-based working-hour records.
From enrollment to the end of treatment at 66 weeks.
Secondary Outcomes (13)
Number of Sickness Absence Episodes
From enrollment to the end of treatment at 66 weeks.
Total Sickness Absence Days from Short Episodes (1-5 days) of Sickness Absence
From enrollment to the end of treatment at 66 weeks.
Short-Term Sickness Absence Episodes (1-5 Days)
From enrollment to the end of treatment at 66 weeks.
Number of Consecutive Shifts
From enrollment to the end of treatment at 66 weeks.
Overtime Hours
From enrollment to the end of treatment at 66 weeks.
- +8 more secondary outcomes
Study Arms (2)
Reduced working hours (36 h)
EXPERIMENTALReduced working hours (36 h) for those who regularly conduct night shift work.
Standard working hours (38 h 15 min)
NO INTERVENTIONStandard working hours (38 h 15 min) for those whose organisation or unit did not choose to participate in the trial.
Interventions
Reduced Working Hours (from 38h15minutes to 36h) for those conducting night shift work regularly
Eligibility Criteria
You may qualify if:
- Employment in one of the participating Finnish wellbeing services counties. Employees working in work units participating in the study. For the primary analyses, employees who work regular night shifts. Employees with available administrative, payroll-based working-hour and employment records.
You may not qualify if:
- Exclusive day workers. Employees performing shift work that does not include night shifts. For the primary analyses, employees not engaged in regular night work.
- Employees not performing regular night work may be included in secondary analyses evaluating workplace-level spillover effects.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Kainuun hyvinvointialue
Kajaani, Finland
Päijät-Hämeen hyvinvointialue
Lahti, Finland
Pohjois-Pohjanmaan hyvinvointialue
Oulu, Finland
Related Publications (11)
Voglino G, Savatteri A, Gualano MR, Catozzi D, Rousset S, Boietti E, Bert F, Siliquini R. How the reduction of working hours could influence health outcomes: a systematic review of published studies. BMJ Open. 2022 Apr 1;12(4):e051131. doi: 10.1136/bmjopen-2021-051131.
PMID: 35365508BACKGROUNDTurunen J, Karhula K, Ropponen A, Shiri R, Hamalainen K, Ervasti J, Koskinen A, Haavisto O, Sallinen M, Pehkonen J, Harma M. Evaluating quick return restrictions on sickness absence in healthcare employees: A difference-in-differences study. Int J Nurs Stud. 2025 Mar;163:104996. doi: 10.1016/j.ijnurstu.2025.104996. Epub 2025 Jan 10.
PMID: 39836993BACKGROUNDTurunen J, Karhula K, Ropponen A, Koskinen A, Hakola T, Puttonen S, Hamalainen K, Pehkonen J, Harma M. The effects of using participatory working time scheduling software on sickness absence: A difference-in-differences study. Int J Nurs Stud. 2020 Dec;112:103716. doi: 10.1016/j.ijnurstu.2020.103716. Epub 2020 Jul 14.
PMID: 32736788BACKGROUNDRopponen A, Hirvonen M, Kuusi T, Harma M. Concurrent Trajectories of Objectively Measured Insufficient Recovery and Workload Among a Cohort of Shift Working Hospital Employees: Quantitative Empirical Research. Nurs Open. 2024 Nov;11(11):e70101. doi: 10.1002/nop2.70101.
PMID: 39571045BACKGROUNDNeubert, S., Bader, C., Hanbury, H., & Moser, S. (2022). Free days for future? Longitudinal effects of working time reductions on individual well-being and environmental behaviour. Journal of Environmental Psychology, 82, 101849. https://doi.org/https://doi.org/10.1016/j.jenvp.2022.101849
BACKGROUNDKrutova O, Koskinen A, Peutere L, Ervasti J, Virtanen M, Harma M, Ropponen A. A Longitudinal Study on Trajectories of Night Work and Sickness Absence among Hospital Employees. Int J Environ Res Public Health. 2022 Jul 3;19(13):8168. doi: 10.3390/ijerph19138168.
PMID: 35805827BACKGROUNDKecklund G, Axelsson J. Health consequences of shift work and insufficient sleep. BMJ. 2016 Nov 1;355:i5210. doi: 10.1136/bmj.i5210.
PMID: 27803010BACKGROUNDIARC Working Group on the Identification of Carcinogenic Hazards to Humans. Night Shift Work. Lyon (FR): International Agency for Research on Cancer; 2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK568195/
PMID: 33656825BACKGROUNDHarma M, Karhula K, Turunen J, Koskinen A, Shiri R, Sallinen M, Vanttola P, Haavisto O, Hakola T, Ropponen A. Working time traffic light recommendations: development, use, and implementation in the Finnish social and healthcare. Ind Health. 2026 May 20;64(3):214-232. doi: 10.2486/indhealth.2025-0082. Epub 2025 Sep 15.
PMID: 40958582BACKGROUNDHarma M, Ropponen A, Hakola T, Koskinen A, Vanttola P, Puttonen S, Sallinen M, Salo P, Oksanen T, Pentti J, Vahtera J, Kivimaki M. Developing register-based measures for assessment of working time patterns for epidemiologic studies. Scand J Work Environ Health. 2015 May 1;41(3):268-79. doi: 10.5271/sjweh.3492. Epub 2015 Mar 19.
PMID: 25788103BACKGROUNDHanbury, H., Illien, P., Ming, E., Moser, S., Bader, C., & Neubert, S. (2023). Working less for more? A systematic review of the social, economic, and ecological effects of working time reduction policies in the global North. Sustainability: Science, Practice and Policy, 19(1), 2222595. https://doi.org/10.1080/15487733.2023.2222595
BACKGROUND
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 17, 2026
First Posted
September 30, 2026
Study Start
September 30, 2026
Primary Completion (Estimated)
February 28, 2028
Study Completion (Estimated)
April 1, 2028
Last Updated
September 30, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared because the study uses employer-owned administrative and payroll-based records containing potentially identifiable employee information. Data sharing is restricted by data protection regulations, data use agreements, and organizational policies of the participating wellbeing services counties.