- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03970174
Care Transition Patient Experience Study With Electronic Tool
March 10, 2020 updated by: Trillium Health Partners
Evaluating the Impact of an Electronic Communication Tool on Patient Experience, ED Visits and Re-hospitalization, and Care Transitions in Hospitalized Patients (Including Those With Dementia): a Mixed Methods Study
Patients being admitted to hospital are becoming more complex and they often require a team of health professionals (doctors from different disciplines, nurses, and allied health professionals) working together to meet their needs.
Effective communication among this team and with patients is essential to providing high quality patient-centered care.
Care Connector is an electronic tool that was developed to help health professionals communicate about patient care with each other.
It also incorporates best practice whenever possible (such as the used of Patient Oriented Discharge Summary [PODS] developed at University Health Network) during care transitions.
We want to understand whether using electronic tools can address the communication issues faced by patients/families, and whether they impact on repeat visits to the Emergency Department or the hospital after discharge.
In this study, we will be asking patients and families who have recently been discharged from hospital to describe their experience with communication and care transitions through a brief telephone survey.
All of them will be discharged from units where Care Connector was used.
However, some of the units would have used the PODS feature while others will not.
A small group will also be invited to participate in an in-depth telephone interview.
The results of this study will be used to improve Care Connector and to enhance communication and patient experience in general.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
In this mixed methods study, we examine how electronic tools impact patient/family experience of communication in hospital and care transitions from hospital to home.
Care Connector is an electronic interprofessional communication and collaboration platform initially designed to address communication challenges faced by interprofessional care team.
It has been augmented to support care transitions through a care transition module (that include the generation of provider-facing discharge summary and PODS).
This study examines the impact of this care transition module on patient/family experience of in-hospital communication and care transitions.
The quantitative component is a controlled study where baseline data is collected on 4 medicine wards.
The care transition module is then introduced to 2 of the 4 medicine wards (intervention) while the other 2 (control) wards continue to operate without the explicit use of the care transition module.
Data is then collected again on all 4 wards to understand impact of patient/family experience, as well as objective outcomes of ED visits and re-admission within 30 days.
A number of care transition process measures will also be obtained.
In the qualitative component, we will interview patients/families, as well as healthcare providers to understand how technology can or cannot address these issues.
Study Type
Interventional
Enrollment (Anticipated)
240
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Mississauga, Ontario, Canada, L5M 2N1
- Trillium Health Partners
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- General medical patients cared for and discharged by the Hospitalist service
- Be 18 years of age and above
- Length of stay for hospitalization is at least 48 hours
- The discharge destination is home (with or without support), or retirement home
- Has the cognitive ability to, or has a substitute decision maker (SDM) (if patient is not capable) able to, provide informed consent for this research study
- Can be contacted by telephone up to 30 days post discharge
- Able to respond to survey questions over telephone (assistance from family member or other caregiver at the time of telephone survey is permitted)
Exclusion Criteria:
- Discharged from a non-Medicine ward (e.g. medicine patient bed spaced to a surgical ward) or from the Emergency Department directly
- Previously participated in this study (in case of re-admission)
- Discharge destination is another acute care facility, rehab, palliative care unit, complex continuing care, long term care, or any other facility not listed in inclusion criteria 4.
- Died in hospital
- Unable to give informed consent due to language barrier and lack of suitable assistance from family members and/or caregivers and/or SDM (if patient is not capable)
- Cannot be contacted by telephone after discharge
- Unable to respond to telephone survey questions for any reason (e.g. hearing impairment, language barrier) and lack of availability of family members and/or other caregivers willing and able to provide assistance
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
Two of the 4 Medicine wards will have implemented the care transition module of Care Connector
|
Care Connector is an electronic interprofessional communication and collaboration tool.
Its features include Physician Sign-Out, documentation, interprofessional care planner, messaging, and flow planner.
The newest module is a care transition module which allows physicians to electronically generate discharge summaries as well as incorporation of allied health recommendation, but also will pull information into the PODS (Patient Oriented Discharge Summary) format designed by University Health Network.
This results in a patient friendly discharge instruction sheet that can be provided to patient.
The intervention arm will have access to the care transition feature, while the control wards do not.
|
|
No Intervention: Control
Remaining 2 of 4 Medicine wards will use all other aspects of Care Connector (except for care transition module)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Care transition measure 3
Time Frame: Up to 30 days post discharge
|
This is a validated measure developed by Coleman et al (Med Care.
2008 Mar;46(3):317-22) to measure quality of care transitions.
It contains 3 questions (please see reference for questions).
|
Up to 30 days post discharge
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
In-hospital communication
Time Frame: Up to 30 days post discharge
|
Subset of questions from the Canadian Patient Experience Survey - Inpatient Care (CPES-IC)
|
Up to 30 days post discharge
|
|
ED visit
Time Frame: 30 days post discharge
|
ED visit to any site at Trillium Health Partners
|
30 days post discharge
|
|
Hospitalization
Time Frame: 30 days post discharge
|
Hospitalization to any site at Trillium Health Partners
|
30 days post discharge
|
|
Presence of follow up plan in discharge summary
Time Frame: At the time of patient discharge (0 days)
|
Binary (yes/no) assessment of whether the dictated discharge summary contains a follow-up plan section.
|
At the time of patient discharge (0 days)
|
|
Proportion of appointments with date/time confirmed at discharge
Time Frame: At time of patient discharge (0 days)
|
Number of appoints with date/time confirmed / total number of appointments
|
At time of patient discharge (0 days)
|
|
Proportion of patients referred to community support services
Time Frame: At time of patient discharge (0 days)
|
Number of patients referred to community support services / total number of patients
|
At time of patient discharge (0 days)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subgroup analysis of patients with dementia
Time Frame: Up to 30 days post patient discharge
|
We will determine whether a patient has dementia by reviewing all dictated consultation notes and discharge summaries in the medical record to look for mention of dementia.
|
Up to 30 days post patient discharge
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Terence Tang, MD, Trillium Health Partners
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Parry C, Mahoney E, Chalmers SA, Coleman EA. Assessing the quality of transitional care: further applications of the care transitions measure. Med Care. 2008 Mar;46(3):317-22. doi: 10.1097/MLR.0b013e3181589bdc.
- Hahn-Goldberg S, Okrainec K, Huynh T, Zahr N, Abrams H. Co-creating patient-oriented discharge instructions with patients, caregivers, and healthcare providers. J Hosp Med. 2015 Dec;10(12):804-7. doi: 10.1002/jhm.2444. Epub 2015 Sep 25.
- Tang T, Lim ME, Mansfield E, McLachlan A, Quan SD. Clinician user involvement in the real world: Designing an electronic tool to improve interprofessional communication and collaboration in a hospital setting. Int J Med Inform. 2018 Feb;110:90-97. doi: 10.1016/j.ijmedinf.2017.11.011. Epub 2017 Nov 22.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 2, 2018
Primary Completion (Actual)
July 31, 2019
Study Completion (Anticipated)
June 30, 2020
Study Registration Dates
First Submitted
May 9, 2019
First Submitted That Met QC Criteria
May 29, 2019
First Posted (Actual)
May 31, 2019
Study Record Updates
Last Update Posted (Actual)
March 11, 2020
Last Update Submitted That Met QC Criteria
March 10, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 828
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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