The Effect of Working at Home to Reduce Risk of Respiratory Infection
1 other identifier
interventional
2,000
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2022
1 active site
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
March 7, 2022
CompletedStudy Start
First participant enrolled
March 14, 2022
CompletedFirst Posted
Study publicly available on registry
March 28, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 30, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2023
CompletedMarch 28, 2022
March 1, 2022
1 year
March 7, 2022
March 25, 2022
Conditions
Keywords
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
EXPERIMENTALParticipants will work from home for first 4 weeks, and at the office for the last 4 weeks
Office for first 4 weeks, and home office for the last 4 weeks
ACTIVE COMPARATORParticipants will work at the office for the first 4 weeks, and from home during the last 4 weeks
Interventions
Working from home
Working at the office
Eligibility Criteria
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
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Atle Fretheim, PhD
Head of Centre for Epidemic Interventions Research (CEIR)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- 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
- Shared Documents
- STUDY PROTOCOL, SAP, ICF
- Time Frame
- After reporting of the trial findings, estimated to June 2023.
The intention is to enable sharing of an anonymised dataset with all interested parties.