NCT05298488

Brief Summary

The researchers will recruit volunteers from various organisations who are willing and able to be randomised to either working from home for 4 weeks followed by working in the office for 4 weeks, or vice versa. The goal is to assess whether working from home has an impact on the risk of symptoms of respiratory infection.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
2,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2022

Geographic Reach
1 country

1 active site

Status
unknown

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

First Submitted

Initial submission to the registry

March 7, 2022

Completed
7 days until next milestone

Study Start

First participant enrolled

March 14, 2022

Completed
14 days until next milestone

First Posted

Study publicly available on registry

March 28, 2022

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2023

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2023

Completed
Last Updated

March 28, 2022

Status Verified

March 1, 2022

Enrollment Period

1 year

First QC Date

March 7, 2022

Last Update Submit

March 25, 2022

Conditions

Keywords

COVID-19Infection controlOffice from homeSocial distancing

Outcome Measures

Primary Outcomes (1)

  • Respiratory infection

    The proportion of participants who report having had symptoms of respiratory disease

    8 weeks

Secondary Outcomes (5)

  • COVID-19

    8 weeks

  • Absenteeism

    8 weeks

  • Secondary cases of respiratory infection

    8 weeks

  • Work-satisfaction

    8 weeks

  • Work-life balance.

    8 weeks

Study Arms (2)

Home office for first 4 weeks, and office for the last 4 weeks

EXPERIMENTAL

Participants will work from home for first 4 weeks, and at the office for the last 4 weeks

Behavioral: Home officeBehavioral: Office

Office for first 4 weeks, and home office for the last 4 weeks

ACTIVE COMPARATOR

Participants will work at the office for the first 4 weeks, and from home during the last 4 weeks

Behavioral: Home officeBehavioral: Office

Interventions

Home officeBEHAVIORAL

Working from home

Home office for first 4 weeks, and office for the last 4 weeksOffice for first 4 weeks, and home office for the last 4 weeks
OfficeBEHAVIORAL

Working at the office

Home office for first 4 weeks, and office for the last 4 weeksOffice for first 4 weeks, and home office for the last 4 weeks

Eligibility Criteria

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

You may qualify if:

  • Over 18 years old
  • Employee in a company/organisation that has agreed to let their employees take part
  • Willing and able to work form home for 4 weeks (most of the time)
  • \- Unable to work from home

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Norwegian Institute of Public Health

Oslo, 0213, Norway

RECRUITING

MeSH Terms

Conditions

Respiratory Tract InfectionsCOVID-19

Interventions

Working Conditions

Condition Hierarchy (Ancestors)

InfectionsRespiratory Tract DiseasesPneumonia, ViralPneumoniaVirus DiseasesCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsLung Diseases

Intervention Hierarchy (Ancestors)

WorkplaceEmploymentSocioeconomic FactorsPopulation CharacteristicsPersonnel ManagementOrganization and AdministrationHealth Services Administration

Study Officials

  • Atle Fretheim, PhD

    Head of Centre for Epidemic Interventions Research (CEIR)

    STUDY DIRECTOR

Central Study Contacts

Petter Elstrom, PhD

CONTACT

Atle Fretheim, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
CROSSOVER
Model Details: The participants will be allocated to either office from home for the first four weeks, followed by working at the office for four weeks, or vice versa.
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 7, 2022

First Posted

March 28, 2022

Study Start

March 14, 2022

Primary Completion

March 30, 2023

Study Completion

September 30, 2023

Last Updated

March 28, 2022

Record last verified: 2022-03

Data Sharing

IPD Sharing
Will share

The intention is to enable sharing of an anonymised dataset with all interested parties.

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
After reporting of the trial findings, estimated to June 2023.

Locations