NCT07848607

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

63
Monitor

Trial Health Score

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

Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
18mo left

Started Sep 2026

Geographic Reach
1 country

3 active sites

Status
not yet recruiting

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 Progress1%
Sep 2026Apr 2028

First Submitted

Initial submission to the registry

September 17, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

September 30, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

September 30, 2026

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2028

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2028

Last Updated

September 30, 2026

Status Verified

September 1, 2026

Enrollment Period

1.4 years

First QC Date

September 17, 2026

Last Update Submit

September 23, 2026

Conditions

Keywords

Working Time ReductionReduced Working HoursNight WorkNight Shift WorkHealthcare WorkersSickness AbsenceEmployee turnoverPayroll-Based Working Hour DataQuasi-experimental Study

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)

EXPERIMENTAL

Reduced working hours (36 h) for those who regularly conduct night shift work.

Other: Reduced Working Hours (from 38h15minutes to 36h)

Standard working hours (38 h 15 min)

NO INTERVENTION

Standard 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

Reduced working hours (36 h)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Päijät-Hämeen hyvinvointialue

Lahti, Finland

Location

Pohjois-Pohjanmaan hyvinvointialue

Oulu, Finland

Location

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: 35365508BACKGROUND
  • Turunen 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: 39836993BACKGROUND
  • Turunen 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: 32736788BACKGROUND
  • Ropponen 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: 39571045BACKGROUND
  • Neubert, 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

    BACKGROUND
  • Krutova 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: 35805827BACKGROUND
  • Kecklund G, Axelsson J. Health consequences of shift work and insufficient sleep. BMJ. 2016 Nov 1;355:i5210. doi: 10.1136/bmj.i5210.

    PMID: 27803010BACKGROUND
  • IARC 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: 33656825BACKGROUND
  • Harma 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: 40958582BACKGROUND
  • Harma 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: 25788103BACKGROUND
  • Hanbury, 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

Annina Ropponen, Professor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants are effectively in one of two concurrent conditions: 1. Reduced working hours (36 h) 2. Standard working hours (38 h 15 min)
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.

Locations