Diabetes Toolkit at Discharge

Sponsor
Northwestern University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05663931
Collaborator
(none)
120
1
2
22.7
5.3

Study Details

Study Description

Brief Summary

The purpose of this randomized clinical trial is to implement the DM Discharge Toolkit into hospital discharge and assess the effect of the DM Discharge Toolkit on patients newly requiring insulin.

Condition or Disease Intervention/Treatment Phase
  • Other: DM Discharge Toolkit
N/A

Detailed Description

This study is a randomized controlled trial with a parallel group design of up to 120 study participants in a 1:1 ratio to receive either current standard of care discharge DM training (control) or current standard of care discharge DM training and the DM Discharge Toolkit (intervention) before or immediately after being sent home to assume self-DM care with insulin.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Implementation and Testing of a Diabetes Discharge Intervention to Improve Safety During Transitions of Care
Actual Study Start Date :
Jan 10, 2023
Anticipated Primary Completion Date :
Oct 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: DM Discharge Toolkit

Up to 60 participants will be recruited for the intervention group. Participants will receive the current standard of care DM education for insulin at Northwestern Memorial Hospital and the adjunctive education with the DM Discharge Toolkit.

Other: DM Discharge Toolkit
The DM Discharge Toolkit is a multi-modal intervention consisting of a 3-D printed DM survival "kit" that stores DM self-care supplies (e.g., glucose meter) and technical skills (e.g., injection) simulation materials (e.g. simulation skin), whose use is integrated with a website (https://mydiabeteskit.com) containing standardized DM "Survival" education content.

No Intervention: Current Standard of Care Discharge DM Training

Up to 60 participants will be recruited for the control group. Participants will receive the current standard of care DM education for insulin use during current discharge care processes at Northwestern Memorial Hospital.

Outcome Measures

Primary Outcome Measures

  1. Mean glucose levels [30 days]

    Mean glucose levels based on home glucose meter and outpatient laboratory data post-discharge

Secondary Outcome Measures

  1. Number of hypoglycemic episodes [14, 30 and 90 days]

    Number of glucoses < 70 mg/dl

  2. Number of hyperglycemic episodes [14, 30 and 90 days]

    Number of blood glucose levels >200 mg/dL

  3. Healthcare utilization [14, 30 and 90 days]

    Number of post-discharge contacts with the healthcare system (i.e. phone calls, emergency room visits, re-admissions, outpatient clinician visits).

  4. HbA1c [90 days]

    Hemoglobin A1c blood test

  5. Time in hyperglycemia [14 days]

    Time in hyperglycemia defined as > 200 mg/dl, outcome from continuous glucose monitor placement

  6. Time in hypoglycemia [14 days]

    Time in hyperglycemia defined as < 70 mg/dl, outcome from continuous glucose monitor placement

  7. Mean amplitude of glycemic excursion [14 days]

    MAGE, outcome from continuous glucose monitor placement

  8. Glycemic variability [14 days]

    A continuous glucose monitor will be used to monitor glucose levels from discharge to 14 days post discharge.

  9. Diabetes Symptoms Questionnaire [14 days, 30 days]

    The Diabetes Symptoms Questionnaire consists of 9 questions where patients answer on a scale between 1-5, with higher numbers indicating a greater rate of occurrence.

  10. Summary of Diabetes Self Care Activities [14 days, 30 days]

    The Summary of Diabetes Self Care Activities consists of 7 questions where patients tally the number of days in the past week that they performed various diabetes self care tasks, such as checking blood glucose and taking medications.

  11. Diabetes Distress Scale [14 days, 30 days]

    The Diabetes Distress Scale is a questionnaire with 17 questions where patients answer on a scale between 1-6, with higher numbers indicating higher distress related to diabetes diagnosis.

  12. Hospital Consumer Assessment of Healthcare Providers and Systems [14 days, 30 days]

    Patient satisfaction survey

  13. Partner Diabetes Distress Scale [Baseline, 30 days, 90 days]

    The Partner Diabetes Distress Scale is a questionnaire with 21 questions where a spouse or partner of someone with diabetes answers on a scale between 0-4, with higher numbers indicating higher distress related to partner's diabetes diagnosis.

  14. Perceived Stress Scale [Baseline, 30 days, 90 days]

    The Perceived Stress Scale is a questionnaire with 10 questions where a patient answers on a scale between 0-4 with higher numbers indicating a greater rate of occurrence.

  15. Infection [30 and 90 days]

    Rate of infection (bacterial, viral, other)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • English speaking patients

  • 18 years of age and older

  • Expected survival >90 days

  • Need for new insulin at time of hospital discharge

Exclusion Criteria:
  • Patients with the inability to give informed consent

  • Non-English speaking

  • Not diagnosed with diabetes

  • Not been newly prescribed insulin

Contacts and Locations

Locations

Site City State Country Postal Code
1 Northwestern Memorial Hospital Chicago Illinois United States 60611

Sponsors and Collaborators

  • Northwestern University

Investigators

  • Principal Investigator: Amisha Wallia, MD, Northwestern University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Amisha Wallia, Associate Professor, Northwestern University
ClinicalTrials.gov Identifier:
NCT05663931
Other Study ID Numbers:
  • STU00216291
First Posted:
Dec 23, 2022
Last Update Posted:
Feb 2, 2023
Last Verified:
Jan 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Amisha Wallia, Associate Professor, Northwestern University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 2, 2023