Impact of Physical Exercise at a Hospital

June 2, 2025 updated by: Stig Molsted, Nordsjaellands Hospital

Impact of Physical Exercise at a Hospital Tested in a Pilot Trial

Aims and Hypotheses Aims

  • to investigate associations between an intelligent exercise training intervention and clinical health parameters, well-being, sick leave and productivity at Nordsjællands Hospital (NOH)
  • to generate data and experiences to a larger cluster randomized trial with more included departments at NOH
  • to analyze how the intervention could be successfully implemented in the organization to ensure long-term effects

Outcomes

  • Aerobic capacity (Åstrand's ergometer test)
  • Blood pressure and heart rate
  • Physical activity (steps measured by tracker)
  • Self-reported health (questionnaire EQ-5D)
  • Self-reported physical activity (questionnaire IPAQ)
  • Well-being (questions from the Danish Health and Morbidity Survey)
  • Musculoskeletal pain and use of anti-pain medications (Numeric Rating Scale)
  • Monetized value of productivity loss
  • Productivity using an employer´s perspective (scale 1-10)
  • Sick leave (days in short term (≤14 days) and long term (>14 days), data will be delivered by The Department of HR)
  • Muscle strength in knee extension (dynamometer)

Intervention The concept of intelligent training at the worksite is an individualized exercise training where the exercises are: 1) balanced to the physiological capacity of the employees relative to their occupational exposure, 2) tailored to the individual capacities and disorders to improve employees' health, 3) motivating by offering evidence based and enjoyable programs implemented with care, and 4) cost-effective for the company.

The intervention period is 20 weeks of intelligent exercise training. Every week, several exercise sessions will be offered to the participants in the intervention group during the working hours. The exercise sessions will be of 30 min durations twice a week and include aerobic exercise with high intensity (≥16 on the Borg scale, rate of perceived exhaustion), resistance training and/or functional training. In addition, there will be a number of intelligent exercise sessions of 30 min durations before and after the most common working hours with a primary focus on aerobic exercise. The exercise sessions will be supervised by exercise experts (education in sport or physiotherapy).

The intelligent exercise interventions will be adjusted to the individual participant's physical capacity and limitations; thus, as one participant may perform aerobic exercise, another person may perform resistance training.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

In this pilot study, we will investigate the potential of physical training at departments at NOH. A large university hospital covering a population of 1,7 mio citizens in the Northern Region of Zealand, and one of eight new Danish "super-hospitals". We will invite all health care workers from the participating departments at the hospital to be enrolled in the study and apply the "intelligent exercise" intervention where each participant will receive a tailored intervention (exercise plan) based on an individual assessment including the mapping of the participant's needs and motivation (2).

References can be found at the end of the document.

Participants The 15 departments will be invited and it is anticipated that 700 employed will volunteer to the study.

All employees (nurses, doctors, secretaries and other staff) in the departments will be invited to the study. The recruitment will follow a strategy with local information at the departments regarding the study intervention and tests.

Intervention The concept of intelligent training at the worksite is an individualized exercise training where the exercises are: 1) balanced to the physiological capacity of the employees relative to their occupational exposure, 2) tailored to the individual capacities and disorders to improve employees' health, 3) motivating by offering evidence based and enjoyable programs implemented with care, and 4) cost-effective for the company.

The intervention period is three months of intelligent exercise training. Every week, several exercise sessions will be offered to the participants in the intervention group during the working hours. The exercise sessions will be of 30 min durations twice a week and include aerobic exercise with high intensity (≥16 on the Borg scale, rate of perceived exhaustion), resistance training and/or functional training (12). In addition, there will be a number of intelligent exercise sessions of 30 min durations before and after the most common working hours with a primary focus on aerobic exercise. The exercise sessions will be supervised by exercise experts (education in sport or physiotherapy).

The intelligent exercise interventions will be adjusted to the individual participant's physical capacity and limitations; thus, as one participant may perform aerobic exercise, another person may perform resistance training (12).

A goal will be that as many as possible will participate in minimum 60 min intelligent exercise training per week.

Prior to the intervention the participants will also be offered motivational support by a special educated staff to increase the level of leisure time physical activity and the level of general physical activity at work.

There will be offered intelligent exercise interventions to those on evening duties.

During the intervention periods, the participants will be supported by trained exercise ambassadors.

Sample size calculation The study will be performed without a sample size calculation, as it is a pilot trial to generate data before the intervention is tested in a larger cluster randomized trial with sufficient power to assess the validity of the results.

Statistical analyses The analyses of the changes of the numeric outcome variables during the study will be assessed using Student's t test if data are normally distributed or Wilcoxon Signed Ranks Test if data are not normally distributed. Changes of categorical variables will be analysed using a Chi2 test.

The associations between groups of staff (nurses, medical doctors and other) and changes of outcome variables (physical activity, productivity, sick leave, physical capacity) will be tested in multiple linear regression models with confounder adjustments.

Results are considered significant (2-tailed) when p<0.05. The statistical analyses will be performed in collaboration with a statistician from Section of Biostatistics, Department of Public Health, University of Copenhagen.

Subjects Every employee (e.g. nurses, doctors, secretaries, lab technician) from the departments at NOH will be invited to the study, but only those who agree in writing will be included.

Short-term and long-term risks, side effects and disadvantages Participants who have not previously been physically active may experience transient side effects such as sore muscles, shortness of breath, etc. There are no immediate risks associated with the intervention, as it is adapted to the physical ability of the individual subject. The therapeutic benefit for participants and future employees justifies an intervention like this.

Biological material None

Processing of personal data in the project The study will be approved by the Danish Data Protection Agency. The collected data will be stored in RedCap according to rules of the data protection agency in the Capital Region. All project data collected, will be handled in accordance with the rules of the Capital Region, in relation to current legislation. No data are sent abroad.

Funding The initiative to plan and execute the study is done by senior researcher associate professor Stig Mølsted and other researchers employed at NOH. The study is supported by NOH with a grant of 50,000 DKK to the initial analysis. In addition, NOH supports the study with other payments including the costs related to the participants' exercise training during the working hours. To ensure the realizability of this study, several funding application initiatives are in the pipeline for 2021-3 and forth, including Danish national and private funds.

Grants will be deposited into a hospital account. Members of the study group will have no financial affiliation with donors.

Remuneration No remuneration is paid to the project participants

Recruitment of subjects and informed consent Potential study participants in the included departments will receive written information about the project explaining the intervention. Oral information will be provided at joint meetings at the hospital to which test subjects are invited. Interested participants will also receive a written consent form. Prior to obtaining the informed consent, it will be ensured that the participants will have time and opportunity to read the information, ask questions and consider whether to participate. If the participant wishes to be included in the study, the consent declaration is dated and signed by the study participant and by the health care professional who provided the information.

Presentation of the results The results should have special interest to hospitals in Denmark and worldwide. The results of the study will also be of interest in other public and private companies.

The study results will be presented at national and international meetings and congresses, in international peer reviewed journals and in public media. Both positive, negative and inconclusive results will be published. The study will be registered at www.clinicaltrials.gov.

Ethics In this scientific experiment, all participants receive a training program tailored to the individual. Each individual participant is being physically pressured to an extent that one must not assume will be of any long-term burden to the participant. If any test results call for further investigations of a participant, the participant will be encouraged to consult the person's general practitioner.

Adverse effects related to the exercise interventions will be registered and evaluated in the study. The therapeutic benefit for participants and future employees justifies an intervention like this, as this intervention is expected to raise public health in general.

Adverse effects related to the exercise interventions will be registered and evaluated in the study.

References

  1. Pedersen BK, Saltin B. Exercise as medicine - evidence for prescribing exercise as therapy in 26 different chronic diseases. Scand J Med Sci Sports 2015 Dec;25 Suppl 3:1-72.
  2. Justesen JB, Sogaard K, Dalager T, Christensen JR, Sjogaard G. The Effect of Intelligent Physical Exercise Training on Sickness Presenteeism and Absenteeism Among Office Workers. J Occup Environ Med 2017 Oct;59(10):942-948.
  3. Jakobsen MD, Sundstrup E, Brandt M, Andersen LL. Psychosocial benefits of workplace physical exercise: cluster randomized controlled trial. BMC Public Health 2017 Oct 10;17(1):798-017-4728-3.
  4. Korshoj M, Birk Jorgensen M, Lidegaard M, Mortensen OS, Krustrup P, Holtermann A, et al. Decrease in musculoskeletal pain after 4 and 12 months of an aerobic exercise intervention: a worksite RCT among cleaners. Scand J Public Health 2018 Dec;46(8):846-853.
  5. Blangsted AK, Sogaard K, Hansen EA, Hannerz H, Sjogaard G. One-year randomized controlled trial with different physical-activity programs to reduce musculoskeletal symptoms in the neck and shoulders among office workers. Scand J Work Environ Health 2008 Feb;34(1):55-65.
  6. Jakobsen MD, Sundstrup E, Brandt M, Jay K, Aagaard P, Andersen LL. Effect of workplace- versus home-based physical exercise on musculoskeletal pain among health care workers: a cluster randomized controlled trial. Scand J Work Environ Health 2015 Mar;41(2):153-163.
  7. van den Berg S, Burdorf A, Robroek SJW. Associations between common diseases and work ability and sick leave among health care workers. Int Arch Occup Environ Health 2017 Oct;90(7):685-693.
  8. European Foundation for the Improvement of Living and Working Conditions. http://www.eurofound.europa.eu/. Absence from work. © European Foundation for the Improvement of Living and Working Conditions, 2010.
  9. Korshoj M, Lidegaard M, Skotte JH, Krustrup P, Krause N, Sogaard K, et al. Does aerobic exercise improve or impair cardiorespiratory fitness and health among cleaners? A cluster randomized controlled trial. Scand J Work Environ Health 2015 Mar;41(2):140-152.
  10. Lidegaard M, Sogaard K, Krustrup P, Holtermann A, Korshoj M. Effects of 12 months aerobic exercise intervention on work ability, need for recovery, productivity and rating of exertion among cleaners: a worksite RCT. Int Arch Occup Environ Health 2018 Feb;91(2):225-235.
  11. Andersen LL, Kjaer M, Sogaard K, Hansen L, Kryger AI, Sjogaard G. Effect of two contrasting types of physical exercise on chronic neck muscle pain. Arthritis Rheum 2008 Jan 15;59(1):84-91.
  12. Sjogaard G, Justesen JB, Murray M, Dalager T, Sogaard K. A conceptual model for worksite intelligent physical exercise training--IPET--intervention for decreasing life style health risk indicators among employees: a randomized controlled trial. BMC Public Health 2014 Jun 26;14:652-2458-14-652.
  13. Danish Health and Medicines Authority. [Specialeplanlægning]. 2015 April;978-87-7104-601-4(1.1).
  14. Danmarks Radio. [Danmarkskort: Her er der størst lægemangel]. 2018; Available at: https://www.dr.dk/nyheder/indland/danmarkskort-her-er-der-stoerst-laegemangel. Accessed 08.29., 2019.
  15. Kristensen MT. [Sundhedsreform kan forværre manglen på prkatiserende læger, hvor den er størst]. 2019(10).
  16. Danmarks Radio. [Lægemangel i uskantsområderne er tredoblet under Lars Løkke]. 2019; Available at: https://www.dr.dk/nyheder/politik/laegemangel-i-udkantsomraaderne-er-tredoblet-under-lars-loekke. Accessed 08.29., 2019.
  17. Pronk NP, Martinson B, Kessler RC, Beck AL, Simon GE, Wang P. The association between work performance and physical activity, cardiorespiratory fitness, and obesity. J Occup Environ Med 2004 Jan;46(1):19-25.
  18. Pereira M, Comans T, Sjogaard G, Straker L, Melloh M, O'Leary S, et al. The impact of workplace ergonomics and neck-specific exercise versus ergonomics and health promotion interventions on office worker productivity: A cluster-randomized trial. Scand J Work Environ Health 2019 Jan 1;45(1):42-52.
  19. Jensen TM, Eriksen SBM, Larsen JS, Aadahl M, Rasmussen SS, Olesen LB, et al. Exercise training is associated with reduced pains from the musculoskeletal system in patients with type 2 diabetes. Diabetes Res Clin Pract 2019 154:124-129.

Study Type

Interventional

Enrollment (Estimated)

700

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Hillerød, Denmark, 3400
        • Recruiting
        • Nordsjællands Hospital
        • Contact:
    • Region Hovedstaden
      • Hillerød, Region Hovedstaden, Denmark, 3400
        • Recruiting
        • Nordsjællands Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

- Employed nurses, doctors, secretaries and other staff on Nordsjællands Hospital, Denmark

Exclusion Criteria:

- If exercise training is not allowed

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
Intervention group that receive 30 min exercise training twice weekly in 20 weeks
Exercise training with aerobic and strength training, 30 min per session

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes of work productivity
Time Frame: Tested before and after 20 weeks intervention
Self-rated in questionaire (1-10 scale)
Tested before and after 20 weeks intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes of personal well-being
Time Frame: Tested before and after 20 weeks intervention
Self-rated in questionaire (likert scale)
Tested before and after 20 weeks intervention
Changes of quality of life
Time Frame: Tested before and after 20 weeks intervention
Self-rated quality of life in the questionaire EQ-5D (scale -0.624 to 1)
Tested before and after 20 weeks intervention
Changes in self-rated physical activity
Time Frame: Tested before and after 20 weeks intervention
Self-rated in the questionaire IPAQ (total METs scores, continous data)
Tested before and after 20 weeks intervention
Changes of muscoloskeletal pain
Time Frame: Tested before and after 20 weeks intervention
Self-rated in questionaire (NRS 0-10)
Tested before and after 20 weeks intervention
Changes of blood pressure
Time Frame: Tested before and after 20 weeks intervention
Resting test of diastolic and systolic pressure (mmHg)
Tested before and after 20 weeks intervention
Changes of aerobic capacity
Time Frame: Tested before and after 20 weeks intervention
Aastrands test (oxygen uptace pr min pr kg body weight)
Tested before and after 20 weeks intervention
Changes of hip/waist ratio
Time Frame: Tested before and after 20 weeks intervention
The circumferences of the hip and waist areas (cm)
Tested before and after 20 weeks intervention
Changes of sick-leave
Time Frame: Tested before and after 20 weeks intervention
Register data for sick-leave (number of days)
Tested before and after 20 weeks intervention
Changes of physical activity
Time Frame: Tested before and after 20 weeks intervention
Tracked by telephones (health app, number of steps)
Tested before and after 20 weeks intervention
Changes of muscle strength
Time Frame: Tested before and after 20 weeks intervention
Muscle strength tested in knee extension (N)
Tested before and after 20 weeks intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Stig Mølsted, PhD, Department of Clinical Research, Nordsjællands Hospital, Denmark

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 16, 2022

Primary Completion (Actual)

December 18, 2023

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

June 29, 2021

First Submitted That Met QC Criteria

July 26, 2021

First Posted (Actual)

August 3, 2021

Study Record Updates

Last Update Posted (Estimated)

June 5, 2025

Last Update Submitted That Met QC Criteria

June 2, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • H-21021866

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.