ClinicalTrials.gg
Status unknownNCT00961987Updated Aug 19, 2009

Innovation to Providing Interprofessional Maternity Care

An interventional study of Collaborative model and Usual care in Pregnancy, sponsored by McMaster University. Status unknown at 1 site in Canada. Open to female participants aged 16 Years to 60 Years. Per ClinicalTrials.gov, last updated 2009-08-19.

Sponsored by McMaster University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2009), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
700
Allocation
Randomized
Ages
16 Years to 60 Years
Sex
Female
01

Study summary

The aim of this pilot project is to determine if there are differences in patient outcomes and healthcare utilization between patients randomly assigned to usual care (a collaborative model of maternity care with co-located healthcare professionals but with referrals to off-site obstetricians) or to a collaborative model of maternity care with co-located healthcare professionals, including obstetricians. It is hypothesized that by creating a seamless interface between obstetrical consultation and ongoing longitudinal maternity care, patient outcomes (birth outcome data), patient satisfaction and healthcare utilization, including number of outpatient visits, ultrasounds, laboratory tests, consultations, etc, will be improved in the intervention group compared with the group receiving usual care. The results could potentially lead to other sites adopting this innovative model of maternity healthcare delivery.

02

Conditions studied

  • Pregnancy

Keywords

  • Maternity care
  • Interprofessional collaboration
  • Continuity of Care
  • Integration
03

In context

Lead sponsor

McMaster University is the lead sponsor of 738 studies on the registry; 125 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 3 (43%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 60 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 16 years of age or older
  • Attending their intake appointment at the Centre
  • Ability to understand English
  • Legal status in Canada

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
700 participants (estimated)

Study arms

  • Experimental
    Collaborative model

    Patients will be referred (if necessary) to an obstetrician who will be co-located in the Maternity Centre and who will be part of the collaborative model of maternity care.

    Other: Collaborative model

  • Active comparator
    Usual care

    At present, if Maternity Centre patients require the specialized services of an obstetrician, the current standard of care is to refer them to obstetricians located offsite with no professional ties to the Maternity Centre

    Other: Usual care

Interventions

  • OtherCollaborative model

    Patients will be referred (if necessary) to an obstetrician who will be co-located in the Maternity Centre and who will be part of the collaborative model of maternity care.

  • OtherUsual care

    At present, if Maternity Centre patients require the specialized services of an obstetrician, the current standard of care is to refer them to obstetricians located offsite with no professional ties to the Maternity Centre

06

What researchers measure

Primary outcomes

  1. Patient outcomes (birth outcomes)

    Time frame: 9 months

Secondary outcomes

  1. Patient satisfaction

    Time frame: 9 months

  2. Healthcare utilization

    Time frame: 9 months

07

Study locations

1 site
  • Maternity Centre
    Hamilton, Ontario L8P 4V1, Canada
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Oct 2009 and a primary completion of Jun 2010. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 18, 2009
First posted
Aug 19, 2009
Start
Oct 2009
Primary completionEst.
Jun 2010
Last update
Aug 19, 2009
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 19, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00961987
First posted
Aug 19, 2009
Start date
Oct 2009
Primary completion
Jun 2010 (estimated)
Last update
Aug 19, 2009

Study contacts

Christine Rodriguez, MSc
Contact
rodrigmc@mcmaster.ca
905-525-9140 ext. 27528
Keyna Bracken, MD
Contact
bracken@mcmaster.ca
905-528-5553
Keyna Bracken, MD
principal investigator · McMaster University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2009. You cannot join it, but the record below documents what was studied.

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