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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
Kaiser Permanente
About
Eligibility
Locations
Arms
Outcomes
Full info

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

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    April 26, 2021
    Last Updated
    April 26, 2021
    Sponsor
    Kaiser Permanente
    Collaborators
    Patient-Centered Outcomes Research Institute
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    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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