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Hand Hygiene Intervention Study in Finnish Garrison

Can Intensified Hand Hygiene Decrease Morbidity and Lost Service Days in a Garrison

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01887730
Acronym
VirusFight
Enrollment
1120
Registered
2013-06-27
Start date
2012-01-31
Completion date
2020-12-31
Last updated
2018-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infections

Keywords

Hand Hygiene, Communicable Diseases, Prevention

Brief summary

In this study the investigators aim to elucidate the possibility to reduce occurrence of infectious diseases in a garrison with enhanced and guided hand hygiene. The investigators will study occurrence and transmission of infections. In addition, the investigators will find out the causative agents of infections in a garrison with virological analyses of naso-pharyngeal and fecal specimens. The costs of lost service days and other expenses due to infectious diseases will be evaluated with a cost analysis study.

Interventions

BEHAVIORALHand washing with soap and water

Can infections be prevented by hand washing with soap and water

BEHAVIORALHand cleaning with alcohol-containing hand rub

Can infections be prevented by hand cleaning with alcohol-containing hand rub. Effect of intervention is assessed by following occurrence of infections

BEHAVIORALControl

Sponsors

Finnish Defense Forces
CollaboratorOTHER_GOV
Finnish Institute for Health and Welfare
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* willingness to attend to the study

Exclusion criteria

* skin diseases which prevent using hand disinfectants

Design outcomes

Primary

MeasureTime frame
Number of infection episodes during basic training period. The periods when a person has been in duty in spite of the infection will be included.8 weeks

Secondary

MeasureTime frame
Length of distinct infection episodes due to infectious disease8 weeks
Length of distinct absence episodes due to infectious disease.8 weeks

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026