Clinical Trials Directory

Trials / Terminated

TerminatedNCT05895253

Safety and Efficacy of Vibro-tactile Feedback for Patients Who Underwent Lower Limb Amputation

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Ludwig Boltzmann Institute for Traumatology - The research center in cooperation with AUVA · Other Government
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Prosthetics research has grown recently, focusing on bionic approaches that restore bodily functions with technical aids. One method involves using prostheses with feedback systems, which measure physical parameters and provide additional information to the user. Saphenus has developed a feedback system called Suralis© that transfers pressure signals from the prosthetic sole to another body region. This clinical investigation aimed to determine if this system improves gait stability and walking. The study analyzed changes in gait and functional balance and gathered patient-reported measures to evaluate the quality of life. This research was open to individuals who have undergone below-knee amputation but no targeted re-innervation surgery and use prosthetics. Participants received the Suralis© feedback system, and the investigators assessed their walking activities. The system measures prosthetic foot sole pressure and converts it into digital signals, triggering vibration stimuli during the stance phase of walking. The investigators collected gait analyses and patient feedback to assess the impact of the feedback system on prosthetic management. The results will help us understand the benefits and effectiveness of this technology for people with amputation.

Detailed description

The investigators conducted a prospective, unblinded crossover trial to compare the effectiveness of a vibration intervention with no intervention. Participants were randomly assigned to one of two sequences: vibration intervention followed by no intervention or vice versa. The intervention involved using the Suralis© vibrotactile ground-contact feedback system for 60 days. The system transmitted ground contact information to the residual lateral thigh, providing sensory feedback. During the control phase, participants received no additional intervention. The washout period lasted seven days. The study collected data during four visits, assessing gait and patient-reported measures. Bayesian generalized linear mixed models were used for data analysis, considering fixed effects (intervention, sequence, and period) and random effects (individuality).

Conditions

Interventions

TypeNameDescription
DEVICEvibrotactile ground-contact feedbackSuralis®, Saphenus Medical Technology (Baden, Lower Austria, Austria)

Timeline

Start date
2021-10-25
Primary completion
2022-05-06
Completion
2022-05-06
First posted
2023-06-08
Last updated
2023-06-13

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT05895253. Inclusion in this directory is not an endorsement.

Safety and Efficacy of Vibro-tactile Feedback for Patients Who Underwent Lower Limb Amputation (NCT05895253) · Clinical Trials Directory