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First Aid by Laypersons - Effect on Mortality and Length of Stay

Førstehjelp Gjort av Lekfolk-effekt på dødelighet og behandlingsforløp (First Aid by Laypersons - Effect on Mortality and Length of Stay)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03191279
Enrollment
1400
Registered
2017-06-19
Start date
2018-08-31
Completion date
2021-08-31
Last updated
2017-06-19

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

Conditions

Bystander, First Aid, Trauma, Wounds and Injury

Keywords

Wounds and injury, Trauma, First aid, Bystander, Laypersons

Brief summary

The study aims to assess the effect of first aid from bystanders on survival, admission length, and need of ICU-stay for trauma victims.

Detailed description

All ambulance services in Norway will be invited to participate. In the participating ambulance services, the personnel of first unit to reach the scene of accident for any emergency response to trauma will register what first aid measures (if any) are indicated and have been performed by the bystanders on the scene up til the point where the ambulance arrives. Hospital data for each case will be retrieved. Those patients who did receive correct first aid will then be compared to those patients who did not receive first aid, and those where first aid was attempted but not correct for differences in share of survivors, length of hospital stay, and need for admission to ICU.

Interventions

PROCEDUREFirst aid

Open airway (head tilt, chin lift), recovery position, staunch of bleeding, prevention of hypothermia, cooling of burn, CPR

Sponsors

University Hospital of North Norway
CollaboratorOTHER
Norsk Folkehjelp
CollaboratorUNKNOWN
Nasjonal kompetansetjeneste for traumatologi (NKT-Traume)
CollaboratorUNKNOWN
University of Tromso
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All emergency response calls to trauma (drownings and hangings included)

Exclusion criteria

* No injury to patient * Non-traumatic condition * Poisonings

Design outcomes

Primary

MeasureTime frameDescription
Admission length3 months after inclusionLength of hospital stay after injury, in days
Survival1 month after inclusion30-day survival, starting from day of injury
Need of ICU stay3 months after inclusionWhether patient is admitted to ICU during admission

Secondary

MeasureTime frameDescription
Length of ICU stay3 months after inclusionLength of ICU stay if patient was admitted to ICU, in days

Other

MeasureTime frameDescription
Whether patients received first aid from bystandersAt time of inclusionIf patients with indicated measures receiving first aid from bystanders, given for each measure and combined
Whether first aid measures were indicated for the patientAt time of inclusionIf first aid measures was indicated, given for each measure and combined

Countries

Norway

Contacts

Primary ContactHåkon Kvåle Bakke, MD, PhD
hakonkvalebakke@gmail.com+4795182294

Outcome results

None listed

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