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Crossing the Divide: Piloting Integrated Care to Reduce Amputations Among Rural Patients With Diabetic Foot Ulcers

Primary Purpose

Diabetic Foot, Diabetic Ulcer of Left Foot, Diabetic Ulcer of Right Foot

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
integrated care model
Sponsored by
University of Wisconsin, Madison
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Diabetic Foot focused on measuring Multidisciplinary care, Integrated care, Rural disparities, Recruitment, Retention

Eligibility Criteria

18 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Healthcare worker inclusion criteria:

    • work at one of three participating clinics as a provider or scheduler/referral coordinator
  • Patient inclusion criteria:

    • primary care provider is participating in the study
    • develops a diabetic foot ulcer

Exclusion Criteria:

  • Healthcare worker exclusion criteria:

    • insufficient overlap between providers and schedulers, as determined by the clinic manager, such that it would be unlikely a potentially eligible patient could be seen by a participating provider and assisted by a participating scheduler for specialty referral in the same visit
  • Patient exclusion criteria:

    • receiving palliative care such that referral to urban centers for aggressive limb salvage would be inappropriate, as assessed by patient PCP
    • insurance does not cover referral to the University of Wisconsin's specialty clinics
    • unable to provide written informed consent

Sites / Locations

  • University of Wisconsin-Madison

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Historical controls

Integrated care

Arm Description

Patients with diabetic foot ulcers cared for by a primary care provider participating in the study prior to launching the integrated care intervention.

Patients with diabetic foot ulcers cared for by a primary care provider participating in the study after launching the integrated care intervention. Only patients who provide informed consent and enroll in the study will be treated with our integrated care model. All other patients with a participating primary care provider will be treated using a standard care model and will not be considered study participants.

Outcomes

Primary Outcome Measures

Proportion of patients receiving guideline-concordant vascular and infectious disease care processes
(proportion of integrated care patients receiving guideline-concordant vascular and infectious disease care within 3 months of their enrollment) minus (the proportion of historical patients receiving guideline-concordant vascular and infectious disease care within 3 months of participant enrollment)

Secondary Outcome Measures

Proportion of patients undergoing amputation
(proportion of integrated care patients undergoing amputation within 3 months of their enrollment) minus (proportion of historical patients undergoing amputation within 3 months of their enrollment), where amputation is defined as major or minor amputation of the ipsilateral lower extremity to the index ulcer

Full Information

First Posted
January 10, 2022
Last Updated
October 10, 2023
Sponsor
University of Wisconsin, Madison
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT05203471
Brief Title
Crossing the Divide: Piloting Integrated Care to Reduce Amputations Among Rural Patients With Diabetic Foot Ulcers
Official Title
Crossing the Divide: Piloting an Integrated Care Model to Bridge Rural-urban Healthcare Systems and Reduce Major Amputations Among Rural Patients With Diabetic Foot Ulcers
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
February 16, 2023 (Actual)
Primary Completion Date
October 2024 (Anticipated)
Study Completion Date
October 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Wisconsin, Madison
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

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
This project directly addresses the escalating national rate of major (above-ankle) amputations due to diabetic foot ulcers; it focuses on rural patients, who face 37% higher odds of major amputation compared to their urban counterparts. The project pilots the first integrated care model adapted to rural settings, an approach that has reduced major amputations in urban settings by approximately 40%. Pilot data will be used to improve recruitment and retention strategies and provide preliminary evidence of efficacy needed to conduct a robust, statewide efficacy trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot, Diabetic Ulcer of Left Foot, Diabetic Ulcer of Right Foot, Amputation
Keywords
Multidisciplinary care, Integrated care, Rural disparities, Recruitment, Retention

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
This is an adaptive study design where recruitment and retention protocols are modified to improve involvement of rural study participants over three waves. Actively enrolled participants receive/ provide care for diabetic foot ulcers using a care algorithm and referral checklist. Results are compared to historical controls.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
237 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Historical controls
Arm Type
No Intervention
Arm Description
Patients with diabetic foot ulcers cared for by a primary care provider participating in the study prior to launching the integrated care intervention.
Arm Title
Integrated care
Arm Type
Active Comparator
Arm Description
Patients with diabetic foot ulcers cared for by a primary care provider participating in the study after launching the integrated care intervention. Only patients who provide informed consent and enroll in the study will be treated with our integrated care model. All other patients with a participating primary care provider will be treated using a standard care model and will not be considered study participants.
Intervention Type
Other
Intervention Name(s)
integrated care model
Intervention Description
The investigators are piloting an integrated care model for rural patients with diabetic foot ulcers. The model uses two tools to promote collaboration between providers: a care algorithm and a referral checklist. The care algorithm will be used by rural primary care providers to guide integrated care addressing glycemic control, vascular disease, wound care, and infection. The referral checklist will be used by rural schedulers who place referrals to urban specialists. It prompts schedulers to fax appropriate supporting documents (e.g. notes, labs, vascular testing results) with the referral request.
Primary Outcome Measure Information:
Title
Proportion of patients receiving guideline-concordant vascular and infectious disease care processes
Description
(proportion of integrated care patients receiving guideline-concordant vascular and infectious disease care within 3 months of their enrollment) minus (the proportion of historical patients receiving guideline-concordant vascular and infectious disease care within 3 months of participant enrollment)
Time Frame
up to 2 years and 3 months
Secondary Outcome Measure Information:
Title
Proportion of patients undergoing amputation
Description
(proportion of integrated care patients undergoing amputation within 3 months of their enrollment) minus (proportion of historical patients undergoing amputation within 3 months of their enrollment), where amputation is defined as major or minor amputation of the ipsilateral lower extremity to the index ulcer
Time Frame
up to 2 years and 3 months
Other Pre-specified Outcome Measures:
Title
Patient recruitment rate
Description
Number of patients who enrolled in the study divided by the number of patients the study team attempted to contact for study recruitment
Time Frame
up to 2 years and 3 months
Title
Patient retention rate
Description
Number of patients who completed the 3-month follow-up telephone call divided by the number of patients who enrolled in the study
Time Frame
up to 2 years and 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Healthcare worker inclusion criteria: Willing to provide informed consent Willing to comply with study procedures Rural providers (primary care physicians at the UW Health Belleville Family Medicine Clinic, diabetes and wound care specialists at Sauk Prairie Healthcare Diabetes and Wound Care Clinic) and schedulers placing referrals. Employed at a participating clinic For rural providers, confirm understanding that they will retain clinical discretion to deviate from the integrated care model if they think it would best serve the patient. Available for the duration of the study Patient inclusion criteria: Able and willing to provide informed consent. Willing to comply with study procedures and be available for the duration of the study. 18 years of age and older. Patient with either type 1 or type 2 diabetes at a participating rural clinic. Develops diabetic foot ulcer during enrollment period. Exclusion Criteria: Healthcare worker exclusion criteria: Insufficient overlap in work schedules between rural providers and scheduler based on clinic manager determination. Patient exclusion criteria: receiving palliative care such that referral to urban centers for aggressive limb salvage would be inappropriate, as assessed by patient rural provider insurance does not cover referral to the University of Wisconsin's specialty clinics Not suitable for study participation due to other reasons at the discretion of the investigators.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Meghan B Brennan, MD
Organizational Affiliation
University of Wisconsin, Madison
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Wisconsin-Madison
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53705
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data collected during the study, after de-identification will be available to researchers for independent verification of study outcomes or to conduct subsequent clinical research, whose proposed use of the data has been approved by an independent review committee identified for this purpose.
IPD Sharing Time Frame
Beginning 9 months after publication of primary outcomes and ending 5 years after that date.
IPD Sharing Access Criteria
Proposals should be directed to the PI, Dr. Meghan Brennan (mbbrennan@medicine.wisc.edu). If approved after review by regulatory counsel, requestors will enter into a formal data sharing agreement. Data will be shared via encrypted single-user file transmission protocol.

Learn more about this trial

Crossing the Divide: Piloting Integrated Care to Reduce Amputations Among Rural Patients With Diabetic Foot Ulcers

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