Comparing the Effectiveness of Two Approaches to Preventing Severe Hypoglycemia in Patients With Type 2 Diabetes (PHT2) (PHT2)
Primary Purpose
Severe Hypoglycemia
Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Proactive Care Management
my hypo compass education program
Sponsored by
About this trial
This is an interventional prevention trial for Severe Hypoglycemia focused on measuring Hypoglycemia, Self-management, Diabetes Mellitus, Type 2, Patient Education
Eligibility Criteria
Inclusion Criteria:
- Age 50 years or older
- Diagnosed with type 2 diabetes
- Receiving primary care at Kaiser Permanente Washington (KPWA)
- Continuously enrolled at KPWA for 24 months prior to baseline and planning to stay with a KPWA health plan for the next 6 months
- At intermediate to high risk for severe hypoglycemia
- History of severe hypoglycemia in the prior 12 months or impaired awareness of hypoglycemia
Exclusion Criteria:
- Inability to give informed consent
- Unable to speak or read English
- Inability or unwillingness to attend online or telephone educational sessions, follow up calls, or to complete outcome assessments
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Proactive Care Management
Proactive Care Management + my hypo compass education program
Arm Description
Outcomes
Primary Outcome Measures
Self-reported severe hypoglycemia
Any self-reported severe hypoglycemia in prior 12 months
Secondary Outcome Measures
Full Information
NCT ID
NCT04863872
First Posted
April 26, 2021
Last Updated
April 26, 2021
Sponsor
Kaiser Permanente
Collaborators
Patient-Centered Outcomes Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT04863872
Brief Title
Comparing the Effectiveness of Two Approaches to Preventing Severe Hypoglycemia in Patients With Type 2 Diabetes (PHT2)
Acronym
PHT2
Official Title
Comparing the Effectiveness of Two Approaches to Preventing Severe Hypoglycemia
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 19, 2021 (Anticipated)
Primary Completion Date
April 30, 2023 (Anticipated)
Study Completion Date
April 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaiser Permanente
Collaborators
Patient-Centered Outcomes Research Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Severe hypoglycemia is the most feared complication of medications used to lower blood glucose levels in patients with diabetes. Severe hypoglycemia, defined as plasma glucose low enough to require assistance, has been linked to poor health-related quality of life, emotional and interpersonal challenges, car accidents, serious falls, cardiovascular events, dementia, and death. Older adults with type 2 diabetes are particularly vulnerable to the complications of severe hypoglycemia. Each year, approximately 11% of patients with type 2 diabetes self-report severe hypoglycemia episodes. An estimated 14% of emergency hospitalizations of older Americans for adverse drug events implicate insulin and 11% implicate oral hypoglycemic agents. One in four diabetes-related hospital admissions is for hypoglycemia.
This study will compare two ways to reduce severe hypoglycemia in people with type 2 diabetes. The two methods to be compared are:
Proactive care management. This will be a nurse outreach call which is similar to the usual care that people with type 2 diabetes get to reduce their risk of severe hypoglycemia, but given in advance rather than in response to a recent severe hypoglycemia event.
The same proactive care management (nurse outreach call) plus enrollment in my hypo compass, a health education program aimed at improving awareness of hypoglycemia and preventing severe hypoglycemia. This program has been shown to reduce severe hypoglycemia in people with type 1 diabetes but has not been tested in persons with type 2.
Our hypothesis is that proactive care management plus my hypo compass will be more effective than proactive care management alone at preventing self-reported severe hypoglycemia in adults with type 2 diabetes at high risk for severe hypoglycemia. The primary outcome will be measured using surveys at the beginning of the study and 14-months later.
Detailed Description
This study is a two-arm (128 per arm), cluster-randomized, comparative effectiveness study of two evidence-based approaches to preventing severe hypoglycemia. We will use a validated Electronic Health Record (EHR)-based tool to identify patients with type 2 diabetes at intermediate to high risk for severe hypoglycemia. Within this population, we will recruit participants who either have impaired awareness of hypoglycemia or self-report a severe hypoglycemia event in the prior 12 months and are 50 years or older. Participants must be members of Kaiser Permanente Washington and identified by the study.
Following randomization, we will compare patients who receive proactive care management from nurses to patients receiving proactive care management plus my hypo compass, a structured educational intervention that reduces the frequency of severe hypoglycemia in individuals with type 1 diabetes. In both groups, we will use proactive care management to assess and provide evidence-based care for impaired awareness of hypoglycemia and other potential contributors to severe hypoglycemia risk.
Our primary outcome is participant-reported severe hypoglycemia, to capture all events, including those not involving clinical care. We will also examine biochemical measures of hypoglycemia measured using continuous glucose monitoring (CGM), participant-reported hypoglycemia awareness, fear of hypoglycemia, and emergency department visits and hospitalizations for severe hypoglycemia. We will conduct a process evaluation to assess the fidelity of implementation and clarify the causal pathway.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Hypoglycemia
Keywords
Hypoglycemia, Self-management, Diabetes Mellitus, Type 2, Patient Education
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
256 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Proactive Care Management
Arm Type
Active Comparator
Arm Title
Proactive Care Management + my hypo compass education program
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Proactive Care Management
Intervention Description
Participants will receive one telephone nurse outreach call with follow up by the nurse or their primary care provider as clinically indicated.
Intervention Type
Behavioral
Intervention Name(s)
my hypo compass education program
Intervention Description
Participants will be enrolled in a structured education program designed to improve hypoglycemia awareness and reduce severe hypoglycemia. The structured program will include 2 online group education sessions, 2 nurse follow up calls and use of glucose and hypoglycemia diaries, delivered over approximately 3 months.
Primary Outcome Measure Information:
Title
Self-reported severe hypoglycemia
Description
Any self-reported severe hypoglycemia in prior 12 months
Time Frame
Baseline and 14 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 50 years or older
Diagnosed with type 2 diabetes
Receiving primary care at Kaiser Permanente Washington (KPWA)
Continuously enrolled at KPWA for 24 months prior to baseline and planning to stay with a KPWA health plan for the next 6 months
At intermediate to high risk for severe hypoglycemia
History of severe hypoglycemia in the prior 12 months or impaired awareness of hypoglycemia
Exclusion Criteria:
Inability to give informed consent
Unable to speak or read English
Inability or unwillingness to attend online or telephone educational sessions, follow up calls, or to complete outcome assessments
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kelly J Ehrlich, MS
Phone
206-287-2381
Email
Kelly.J.Ehrlich@kp.org
First Name & Middle Initial & Last Name or Official Title & Degree
James Ralston, MD, MPH
Phone
206-287-2076
Email
James.D.Ralston@kp.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Ralston, MD, MPH
Organizational Affiliation
Kaiser Permanente Washington
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Comparing the Effectiveness of Two Approaches to Preventing Severe Hypoglycemia in Patients With Type 2 Diabetes (PHT2)
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