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Maternity early warning score and the frequency of vital sign measurement in maternity patients

In maternity patients does the introduction of a maternity early warning score have an impact on frequency of vital sign measurement and medical practitioner review.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000617066
Enrollment
800
Registered
2010-07-28
Start date
2010-08-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The study is to examine the impact of early warning scores, observation charts and education on the measurement of vital signs and subsequent review by medical staff.

Interventions

1)Maternity early warning scores- this is a track and trigger system to detect vital signs that are outside the normal ranges expected and will be calculated when vital signs are done 2)a new observation chart- this will incorporate the early warning score as well as other information specific to maternity in-patients such as per vagina(pv) loss, protein in urine 3)education program about deteriorating maternity pateints including prelearning with a CD an manual and a 2 1/2 hour face to face ses

1)Maternity early warning scores- this is a track and trigger system to detect vital signs that are outside the normal ranges expected and will be calculated when vital signs are done 2)a new observation chart- this will incorporate the early warning score as well as other information specific to maternity in-patients such as per vagina(pv) loss, protein in urine 3)education program about deteriorating maternity pateints including prelearning with a CD an manual and a 2 1/2 hour face to face session with lecture and case studies The intervention period will run for 4 months once 50% of the clinical staff have completed the education program.

Sponsors

ACT Health
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Maternity pateints admitted as an inpatient 18 years and older

Exclusion criteria

Under 18 years of age

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026