- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02783131
Does Mednav, a Medical Navigation System, Aid Non-technical and Technical Skills in the Simulated Obstetric Emergency?
Study Overview
Detailed Description
Potential participants will be identified by those attending mandatory training/teaching. 2 weeks before their mandatory training they will be emailed with the study information leaflet and a link to a video which explains how to use Mednav. On the morning of the mandatory training/teaching they will be approached by the practice development midwife/Chief or Principle investigator who will give them a copy of the consent form and again the study information leaflet and show the Mednav video. Eligibility criteria will be checked and the study explained, before taking written informed consent.
Participants will personally sign and date the consent form, before any study specific procedures are performed.
Once the team is decided, the investigators will then randomise them to use of Mednav or no mednav, The participants will then undertake a simulated management of post partum haemorrhage which will be recorded for later review. Faculty will record the timing of completion of key technical skills.
A team of 8 assessors will review these simulated scenario recordings. Assessors will complete validated questionnaires to assess teamwork. Assessors will be asked to complete a technical skills list, showing timing and completion of various technical aspects of managing post partum Haemorrhage.
The end of the study will be when the required sample size has been recruited or significance found on interim data analysis.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Staff undertaking mandatory training at chelsea and westminster hospital
Exclusion Criteria:
- Non Consenting.
Study Plan
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MedNav
Team getting taught to use mednav, and using mednav in simulation managing Post partum Haemorrhage.
|
MedNav is a tablet based platform device that acts to help teams manage emergencies.
In the way that satellite navigation devices have replaced maps on journeys mednav has replaced paper based checklist and guidelines to give teams real-time guidance as the emergency happens.
In supports teams by deligating, prompting and scribing as the emergency unfolds.
The intervention arm will be taught how to use this device over 30 minutes and then use it in a simulated scenario managing a post partum haemorrhage.
Other Names:
|
|
No Intervention: non MedNav
Team undergoing routine simulation training in Post Partum Haemorrhage.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical Teamwork Scale
Time Frame: From date of randomisation to 72 weeks, each video will last 20 minutes. Assessors will review the videos at 12 weekly intervals at a sessions that last for up to 3 hours.
|
A 15 point clinical teamwork scale that measures teamwork.
This has separate points of: overall team work, communication, situation awareness, decision making, role responsibility, patient friendly.
Scores for each section are between 0-10.
0 unacceptable, 1-3 Poor, 4-6 Average, 7-9 Good, 10 perfect.
Validated for 3 assessors.
|
From date of randomisation to 72 weeks, each video will last 20 minutes. Assessors will review the videos at 12 weekly intervals at a sessions that last for up to 3 hours.
|
|
Global Assessment of Team Performance
Time Frame: From date of randomisation to 72 weeks, each video will last 20 minutes. Assessors will review the videos at 12 weekly intervals at a sessions that last for up to 3 hours.
|
A 6 point scoring system with these subsections: Communication with patient and partner, Task management, Teamwork, Situational Awareness,Communication, Environment of Room.
Each section is measured on a 5 point rating scale (1 poor performance, 5 excellent performance).
|
From date of randomisation to 72 weeks, each video will last 20 minutes. Assessors will review the videos at 12 weekly intervals at a sessions that last for up to 3 hours.
|
|
Technical Skill Achievement and timing
Time Frame: From date of randomisation to 72 weeks, each video will last 20 minutes. Assessors will review the videos at 12 weekly intervals at a sessions that last for up to 3 hours.
|
A set of 11 key skills for managing a post partum haemorrhage.
Massive obstetric haemorrhage call, Explore trauma, Palpate uterus, Examine placenta, IV Fluids started, Uterotonic started, Bloods taken and sent, Foley Cather inserted, Bimanual compression commenced, Blood transfusion commenced, Decision to move to theatre.
Completion and time since emergency buzzer completion.
This will be in the form of a table, which will include the skill and the time at which each skill is achieved.
These timings will be recorded by the faculty of the simulation session.
|
From date of randomisation to 72 weeks, each video will last 20 minutes. Assessors will review the videos at 12 weekly intervals at a sessions that last for up to 3 hours.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
System Usability Score
Time Frame: From date of randomisation to 72 weeks, each simulation participant using mednav will answer the questionaire which will take 10 minutes.
|
A validated usability score that gives results that can be interoperated into how 'usable' MedNav is.
|
From date of randomisation to 72 weeks, each simulation participant using mednav will answer the questionaire which will take 10 minutes.
|
Collaborators and Investigators
Investigators
- Study Director: shane p Duffy, MBCHB MRCOG, Chelsea and Westminister NHS Foundation Trust
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- C&W14/094
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Postpartum Hemorrhage,
-
Dangana Zakari AdekaWest African College of Surgeons (WACS)CompletedPostpartum Hemorrhage (PPH) | Postpartum Hemorrhage Third Stage of Labour Retained PlacentaNigeria
-
University Hospital, Clermont-FerrandUnknownPostpartum Depression | Postpartum Hemorrhage | Postpartum Women | Postpartum Stress | Postpartum AnxietyFrance
-
ResQ Medical LtdRecruitingPPH | Postpartum Hemorrhage \(PPH\) | Postpartum Hemorrhage \(Primary\)Kenya
-
Cairo UniversityUnknownHemorrhage, PostpartumEgypt
-
Columbia UniversityCompletedHemorrhage, PostpartumUnited States
-
Ain Shams Maternity HospitalUnknownHemorrhage PostpartumEgypt
-
Samuel Lunenfeld Research Institute, Mount Sinai...RecruitingPostpartum Hemorrhage (Primary)Canada
-
Megan LordThermaSENSE CorpCompletedHemorrhage | Vasoconstriction | Hemorrhage, PostpartumUnited States
-
Gynuity Health ProjectsAga Khan Health ServicesCompletedPostpartum Hemorrhage (PPH)Afghanistan
-
KOKO Medical Inc.RecruitingPostpartum Hemorrhage | Hemorrhage, Postpartum | Immediate Postpartum HemorrhageUnited States
Clinical Trials on MedNav
-
Chelsea and Westminster NHS Foundation TrustCompletedInfant Showing No Response to ResuscitationUnited Kingdom