GoldiCare: Can Work be Organized to Become More Health Promoting for Employees in Home Care Services?

Sponsor
Norwegian University of Science and Technology (Other)
Overall Status
Recruiting
CT.gov ID
NCT05487027
Collaborator
Norwegian Labour and Welfare Administration (Other), Trondheim Kommune (Other)
200
11
2
5.8
18.2
3.1

Study Details

Study Description

Brief Summary

This is a two-group, cluster randomized controlled trial designed to assess a health promoting intervention in the home care sector. The intervention aims to evenly distribute the patients requiring high levels of demanding care across all workers on the units, which may lower the working strain and thus the incidence of musculoskeletal pain. The two groups in the study will be a control group and an intervention group. The intervention will last for approximately 4 months.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Goldilocks work principle
N/A

Detailed Description

This is a two-group cluster randomized controlled trial to compare an organizational intervention to control. The home care units will be treated as clusters to avoid contamination within units.

Control group: No intervention, their work will continue as usual without any instructions from researchers.

Intervention group: The intervention will consist of the operational managers distributing the physically strenuous shifts evenly between the workers in each home care unit. This will be achieved using a tool developed in Microsoft Excel which gives an overview over how much strain we expect each shift to have and gives a score on how well the operational manager distributes the strain between employees.

The intervention will last for approximately 4 months, depending on duration of pre and post measurements.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Individuals are grouped in clusters, where the clusters are the home care units in Trondheim. Half of the units will be randomized to control, half will be randomized to intervention. All units will be randomized at the same time.Individuals are grouped in clusters, where the clusters are the home care units in Trondheim. Half of the units will be randomized to control, half will be randomized to intervention. All units will be randomized at the same time.
Masking:
None (Open Label)
Masking Description:
No masking will be possible as the home care units will have an integral part in applying the intervention. The investigators will need to have control over the units in intervention arm as they may need to assist in the early stages of intervention.
Primary Purpose:
Prevention
Official Title:
Can Work be Organized to Become More Health Promoting for Employees in Home Care Services?
Anticipated Study Start Date :
Aug 22, 2022
Anticipated Primary Completion Date :
Feb 15, 2023
Anticipated Study Completion Date :
Feb 15, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

This arm will have no intervention or instructions from researchers. Participants in this arm will perform their work planning as normal.

Experimental: Intervention

Introduce a deliberate variation between workers in how much they care for physically strenuous users. Some workers may receive more strenuous work compared to before, some less.

Behavioral: Goldilocks work principle
Using the Goldilocks work principle we have tried to find the "just right" distribution of physical strain in the home care sector. This is an intervention to test if it possible to distribute the physical strain experienced in the home care sector in a way that may be more health promoting for the workers.

Outcome Measures

Primary Outcome Measures

  1. Between group changes in musculoskeletal pain in the neck and shoulder from pre to post measurement [7 days during baseline measurements, 7 days during post measurements]

    The workers will rate their musculoskeletal pain in the neck and shoulder area after each working day for a week. The measurement will be repeated at the end of the intervention to assess any changes in the experience of musculoskeletal pain. The question assessing musculoskeletal pain in shoulder and neck area is phrased as "How much pain did you have in your shoulder/neck at the end of this working day?" (Translated from Norwegian).

  2. in musculoskeletal pain in the lower back from pre to post measurement [7 days during baseline measurements, 7 days during post measurements]

    The workers will rate their musculoskeletal pain in the lower back after each working day for one week. The measurement will be repeated at the end of the intervention to assess any changes in the experience of musculoskeletal pain. The question assessing musculoskeletal pain in the lower back area is phrased as "how much pain did you have in your lower back at the end of the working day?" (Translated from Norwegian).

Secondary Outcome Measures

  1. Between group changes in the composition of time spent standing, arms elevated and trunk inclined [7 days during baseline measurements, 7 days during post measurements]

    The difference in physical behavior composition from baseline measurements to post measurements between control and intervention group. The specific variables will be time spent standing, arms elevated, and trunk inclined.

  2. Between group changes in fatigue at end of shift [7 days during baseline measurements, 7 days during post measurements]

    The difference between intervention and control group from pre- to post-measurements in how fatigued the workers were at the end of the shift.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Home care worker in one of the included home care units in Trondheim municipality.

  • More than or equal to 50% working position at the home care unit.

Exclusion Criteria:
  • Physically incapable of performing day to day tasks.

  • Any illness during the measurement week

  • Pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bergheim hjemmetjeneste Trondheim Trøndelag Norway
2 Heimdal Hjemmetjeneste Trondheim Trøndelag Norway
3 Klæbu hjemmetjeneste Trondheim Trøndelag Norway
4 Lade hjemmetjeneste Trondheim Trøndelag Norway
5 Nidarvoll hjemmetjeneste Trondheim Trøndelag Norway
6 Nidelven hjemmetjeneste Trondheim Trøndelag Norway
7 Saupstad hjemmetjeneste Trondheim Trøndelag Norway
8 Spongdal hjemmetjeneste Trondheim Trøndelag Norway
9 Strinda Hjemmetjeneste Trondheim Trøndelag Norway
10 Strindheim hjemmetjeneste Trondheim Trøndelag Norway
11 Valentinlyst hjemmetjeneste Trondheim Trøndelag Norway

Sponsors and Collaborators

  • Norwegian University of Science and Technology
  • Norwegian Labour and Welfare Administration
  • Trondheim Kommune

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT05487027
Other Study ID Numbers:
  • 315556
First Posted:
Aug 4, 2022
Last Update Posted:
Aug 25, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 25, 2022