Peer Support for Patients With Diabetic Foot Ulcers

NCT06004219 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2023-12-06

No results posted yet for this study

Summary

The objective of the study is to develop a peer support program that helps improve ulcer care in patients with a diabetic foot ulcer (DFU).Diabetes, peripheral arterial disease (PAD), foot ulceration, and subsequent amputation are unevenly patterned in terms of racial/ethnicity, socioeconomic status, health insurance, and geographic area. The project will identify opportunities to reduce health disparities among economically marginalized patients regarding DFU outcomes.

Conditions

  • Diabetic Foot Ulcer
  • Diabetic Wound
  • Diabetes Mellitus, Type 2
  • Diabetic Foot
  • Diabetes Complications
  • Peripheral Neuropathy

Interventions

BEHAVIORAL

Peer counseling group

A community advisory board (CAB) will be set up for need assessment and to design the peer support program. Virtual meetings will be held quarterly for year 1 and 2. The group will consist of (up to 12 members) and will include at least 2 patient partners (patients with a recently diagnosed ulcer), 2 peer pals (patients with a healed DFU), family members or caregivers (limited to only 1 person per family represented on the CAB), healthcare workers (podiatrist, nurse, or case manager), medical equipment company representatives, and others. We will ask them about potential barriers at the first meeting, have flexible meeting times, and intentionally limit the number of healthcare providers. At the last meeting, we will seek feedback and input from the CAB. In addition, this group will have the opportunity to participate in a focus group which will be moderated with a trained, bilingual assistant and will last 40-60 minutes.

Sponsors & Collaborators

  • University of Southern California

    collaborator OTHER
  • Vascular Cures

    collaborator OTHER
  • Department of Health and Human Services

    collaborator FED
  • Rancho Los Amigos National Rehabilitation Center

    collaborator OTHER
  • Casa Colina Hospital and Centers for Healthcare

    lead OTHER

Principal Investigators

  • Emily Rosario, PhD · Casa Colina Hospital and Centers for Healthcare

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-11-21
Primary Completion
2024-10-31
Completion
2025-01-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06004219 on ClinicalTrials.gov