Feasibility and Effectiveness of a Remote Monitoring Program for the Treatment of Diabetic Foot Ulcers
Diabetic Foot, Diabetic Foot Ulcer, Wound; Foot
About this trial
This is an interventional supportive care trial for Diabetic Foot
Eligibility Criteria
Inclusion Criteria:
- Male or female, aged ≥ 18 years old
- In treatment for lower extremity wound related to diabetic foot ulcer
- Able and willing to use a smartphone to assess the wound for the duration of the study
- English language proficiency
Exclusion Criteria:
- Patients with less than 1 dressing change per week
- Patients with wound size that cannot be covered with a single app scan (out of boundary conditions include wounds that wrap around patient's entire leg)
- Patients with wounds in an inaccessible location who live without a caregiver to assist in taking wound scans
Sites / Locations
- Johns Hopkins University School of MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Standard care
Remote wound monitoring technology
Patients randomized to receive standard of care will be provided with a wound care plan at the time of enrollment, and then follow-up in clinic on a biweekly basis (week 2, 4, 6, 8, 10, 12) for a wound check and care plan update as needed.
Enrolled patients (and their caregivers, if applicable) are given an in-person training on how to use the smartphone app to self-assess their wound during regular dressing changes. Wound assessments are electronically transmitted to a secure, dedicated portal up to once a week for remote review by the study doctors. In-person follow-up is monthly (at the time of enrollment, week 4, week 8, and week 12).