Actively Recruiting
Smart Boot Use to Measure Offloading Adherence
Led by University of Southern California · Updated on 2026-01-16
210
Participants Needed
4
Research Sites
232 weeks
Total Duration
On this page
Sponsors
U
University of Southern California
Lead Sponsor
U
University of California, Los Angeles
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to help people with diabetes who develop neuropathic diabetic foot ulcers (DFUs). These ulcers, or sores, if left untreated can increase the chance of amputation. Part of the treatment is to have the person wear a diabetic shoe or boot to help their foot heal. Sometimes people don't wear the boot like they are told. The investigators want to compare three different kinds of diabetic boots to see if they can help make it easier for people to wear their boots as instructed. The investigators will look at three groups of participants: the first group will use removable offloading with reinforced education emphasizing continuous wear, including during rest and sleep, and not to remove it at any time. The second group will use removable offloading consistent with standard of care and receive education on recommended wear during walking or standing, with permission to remove the device during rest and sleep. The third group will use a smart removable offloading device that provides real-time adherence feedback via a smartwatch and smartphone, with additional personalized education informed by remotely monitored adherence data. The investigators will also be looking at how much physical activity, like walking, the participants do. And they will compare how well participants sleep and rate their quality of life in the three different boots. The investigators think that giving participants information about how much they are wearing their boot using readily available technology will help them to follow the doctor's directions better, and help their wounds heal faster.
CONDITIONS
Official Title
Smart Boot Use to Measure Offloading Adherence
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female
- 18 years old or older
- Have a non-infected, non-ischemic diabetic foot ulcer requiring offloading
- Able to walk at home with or without assistance
- Willing and able to provide written informed consent
You will not qualify if you...
- Wound present for more than 1 year
- HbA1c greater than 12%
- Ankle Brachial Index of less than 0.6 or non-detectable Doppler in affected limb, or planned revascularization during study
- Acute Charcot neuropathy or major foot deformity preventing use of the smart boot
- Amputation above the rearfoot on the affected foot
- Any significant medical or psychiatric condition
- Laboratory abnormalities interfering with study participation
- Currently taking part in exercise training
- Changes in psychotropic or sleep medications within the last 6 weeks
- Ulcer involving bone
- Ulcer not caused by diabetes
- Unable or unwilling to attend clinic visits or follow study protocol
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 4 locations
1
Rancho Los Amigos National Rehabilitation Center
Downey, California, United States, 90242
Actively Recruiting
2
Verdugo Hills Hospital of USC
Glendale, California, United States, 91208
Actively Recruiting
3
Clemente Clinical Research
Los Angeles, California, United States, 90033
Actively Recruiting
4
Keck Medical Center of USC
Los Angeles, California, United States, 90033
Actively Recruiting
Research Team
F
Fabiola Rodriguez, MD
CONTACT
B
Bijan Najafi, PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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