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NCT06096311 Clinical Trial

Improvement of Hyperglycemia/Diabetes in Patients to Improve Safety

Diabetes Mellitus, Type 2 Clinical Trial

Official title:
Improvement of Hyperglycemia/Diabetes in Patients to Improve Safety

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06096311
Other study ID # STU00090319
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2022
Est. completion date December 1, 2024

Study information
Verified date October 2023
Source Northwestern University
Contact Amisha Wallia, MD
Phone 312-503-2756
Email a-wallia@northwestern.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Recruiting
Enrollment 30
Est. completion date December 1, 2024
Est. primary completion date December 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Interviews
Interviews

Locations
Country Name City State
United States Northwestern University Chicago Illinois

Sponsors (1)
Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Qualitative Results from Interviews Participants will be asked to provide their thoughts on potential interventions for a future clinical trial. Up to one year
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