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Clinical Trials/NCT06096311
NCT06096311
Recruiting
Not Applicable

Improvement of Hyperglycemia/Diabetes in Patients to Improve Safety

Northwestern University1 site in 1 country30 target enrollmentApril 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes Mellitus, Type 2
Sponsor
Northwestern University
Enrollment
30
Locations
1
Primary Endpoint
Qualitative Results from Interviews
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this project is to bring together staff and clinicians from Northwestern University/Northwestern Medical Group/Northwestern Memorial Hospital as well as patients and caregivers to assess and redesign the identification and management of hyperglycemia and diabetes during and in transitions of care. There will be 3 different groups for the study: a group of providers [Group 1], a group of patients/caregivers and laypersons [Group 2], and a stakeholder group [Group 3]. Participants will be asked to provide input on potential interventions for a future clinical trial.

Registry
clinicaltrials.gov
Start Date
April 1, 2022
End Date
December 1, 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amisha Wallia

Associate Professor

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • Provider Group: Multidisciplinary clinical team (including but not limited to inpatient endocrine nurse practitioners, nurse coordinators, diabetes educators, outpatient nurses, attending physicians, and pharmacists)
  • Patient, Caregiver and Layperson Group: Patients must have had hyperglycemia or diabetes at Northwestern Memorial Hospital in the last 5 years.
  • Stakeholder Group: Involved in the specific care delivery of diabetes

Exclusion Criteria

  • Provider Group: None
  • Patient, Caregiver, and Layperson Group: Patients will be excluded if they did not have diabetes or had hyperglycemia.
  • Stakeholder Group: None

Outcomes

Primary Outcomes

Qualitative Results from Interviews

Time Frame: Up to one year

Participants will be asked to provide their thoughts on potential interventions for a future clinical trial.

Study Sites (1)

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