Cognitive Aids With Roles Defined (CARD) for Obstetrical Crises: A Multisite Cohort Study

Sponsor
Ottawa Hospital Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT02093078
Collaborator
Canadian Anesthesiologists' Society (Other), The Ottawa Hospital Academic Medical Association (Other)
346
1
48
7.2

Study Details

Study Description

Brief Summary

Crisis resource management represents the set of non technical skills, such as communication, leadership, delegation, and prioritization, that allow effective teamwork for optimal patient care during an urgent and critical situation. The Cognitive Aids with Roles Defined (CARD) is a new concept of cognitive aid addressing the well-documented issue of teamwork in crisis management. It relies on large identification cards specially designed for each team members profession and role. During a life threatening clinical situation, the CARD protocol focuses on clarification of individual roles and distribution of tasks for crisis management rather than creating an additional algorithm identifying either a list of actions to be taken or the dose of a medication. This study aims to evaluate the clinical impact of introducing the CARD protocol in obstetrical emergency situations ("code 333") in clinical practice at The Ottawa Hospital.

Hypothesis: CARD protocol will: (i) decrease the total time taken to deliver the baby, and (ii) improve clinical outcome for the mother and baby compared to traditional management without the CARD protocol.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: CARD

Detailed Description

The CARD protocol offers an innovative yet simple solution to the barriers in crisis management that the literature has already identified. The study is part of a research program investigating strategies to improve crisis management. After completing several simulation studies on cognitive aids, crisis management debriefing, and a pilot CARD study, the investigators aim to explore and investigate the impact of an intervention on patient care.

The concept of a self-organizing team with explicitly defined roles may enhance patient safety. The CARD approach to crisis management is relevant to a broad number of situations, disciplines, and professions. The CARD protocol is easily exportable to any critical situation including intra-hospital arrest, trauma, or critical care patients. The concept of a self-organizing team with defined roles may ultimately enhance patient safety.

The investigators anticipate that their proposal will challenge the traditional way of thinking about cognitive aid, and may advance the theory in the two fields of cognitive aid and team work for crisis management.

The CARD cards with their associated roles and list of tasks will be specifically designed for code 333. In the 'baseline' phase, a research assistant will review Birthing Unit records daily to determine if a code 333 had been called in the preceding 24 hours. Outcome measures will be collected to establish baseline team performance. In order to account for the 'team training effect' and identify the 'CARD effect', both groups will receive didactic and simulation crisis management teaching, but training at the "case site" will include CARD teaching while the contemporaneous "control site" will receive team training without CARD. After the training period at both sites, CARD will be implemented at the "case sight" for code 333s while the "control site" will continue without CARD. Maternal and neonatal outcomes as well as team performance (times to delivery) will continue to be prospectively collected throughout.

Study Design

Study Type:
Observational
Actual Enrollment :
346 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Cognitive Aids With Roles Defined (CARD) for Obstetrical Crises: A Multisite Cohort Study
Study Start Date :
Jan 1, 2014
Actual Primary Completion Date :
Dec 31, 2017
Actual Study Completion Date :
Dec 31, 2017

Arms and Interventions

Arm Intervention/Treatment
CARD

Intervention: CARD This group will be introduced to the CARD protocol which focuses on clarification of individual roles and distribution of tasks. It relies on large identification cards specially designed for each team member's profession and role. Each card worn by a team member identifies the specific tasks associated with that individual's role. CARD enables the team leader and other team members to quickly recognize everyone's role at the code, and each team member can commence their assigned tasks without delay.

Behavioral: CARD
Intervention: CARD This group will be introduced to the CARD protocol which focuses on clarification of individual roles and distribution of tasks. It relies on large identification cards specially designed for each team member's profession and role. Each card worn by a team member identifies the specific tasks associated with that individual's role. CARD enables the team leader and other team members to quickly recognize everyone's role at the code, and each team member can commence their assigned tasks without delay.

Control Arm

Outcome Measures

Primary Outcome Measures

  1. Total Time to Delivery After a Code 333 [from the time of calling in a code 333 to the time of birth (up to 1 day).]

    The primary outcome measure is the exact time from when the code 333 is called, to the time of delivery (up to 1 day).

Secondary Outcome Measures

  1. standard clinical outcomes on patient charts [participants will be followed from when the code 333 was called until hospital discharge or mortality, whichever comes first (up to 3 years).]

    The clinical outcomes on patient charts include: Baby's status: Apgar score, at 1 and 5 minutes Arterial potential hydrogen (pH) of the cord at birth Unplanned admission to intensive care for the baby Infant status at 1 hour of age Length of stay of the baby in hospital Mortality Mother clinical outcomes: Unplanned admission to ICU for the mother Length of stay of the mother in hospital Mortality

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • must hold a staff position at The Ottawa Hospital (Civic or General campus) in one of the following positions:
  1. registered nurses (RN)

  2. operating room attendant

  3. respiratory therapist (RT)

  4. assisting anesthesia

  5. RT assisting neonatal

  6. neonatal RNs

Exclusion Criteria:
  • not a staff member at The Ottawa Hospital (Civic or General campus)

  • holding a position that is different from any of the following: registered nurse, operating room attendant, respiratory therapist, assisting anesthesia, RT assisting neonatal, neonatal RN

  • investigators involved in the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Ottawa Hospital Ottawa Ontario Canada

Sponsors and Collaborators

  • Ottawa Hospital Research Institute
  • Canadian Anesthesiologists' Society
  • The Ottawa Hospital Academic Medical Association

Investigators

  • Principal Investigator: Sylvain Boet, MD, The Ottawa Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ottawa Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT02093078
Other Study ID Numbers:
  • 20120926-01H
First Posted:
Mar 20, 2014
Last Update Posted:
Sep 7, 2018
Last Verified:
Sep 1, 2018
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 7, 2018