Caesar Foot Take-Home Validation Testing

The rationale for this study is to conduct a take-home clinical trial to evaluate the impact of the bimodal Caesar foot in a real-world environment. Participants will take the device home and use it throughout their daily life for two months. A one-month baseline period, using their usual foot, will be completed both before and after the two-month period with the Caesar foot condition. Self-report surveys and performance-based measures will be collected in the clinic at the end of each condition. The intent of this study is to determine the Caesar foot's feasibility in a real-world environment. Data will be collected to understand impact to the user's daily life and physical activity through outcomes and participant feedback. The feedback obtained during this study will be essential to informing the design intended for commercialization.

NCT Number	NCT07075198
Lead Sponsor	Liberating Technologies, Inc. Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Hanger Clinic: Prosthetics & Orthotics, WillowWood, University of Hartford
Conditions	Prosthesis User, Lower Limb Amputation Below Knee (Injury)
Enrollment	18 participants
Start Date	2025-10
Primary Completion	2026-08 (estimated)
Study Completion	2026-08 (estimated)
Updated on ClinicalTrials.gov	2025-10-14