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Vibro-tactile Pressure Feedback of the Prosthetic Foot for Trans-tibial Amputees

Vibro-tactile Pressure Feedback of the Prosthetic Foot for Trans-tibial Amputees

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03965663
Enrollment
13
Registered
2019-05-29
Start date
2020-07-31
Completion date
2022-03-31
Last updated
2020-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amputation

Brief summary

The aim of the study is to investigate the influence of a vibro-tactile device on trans-tibial amputees in terms of gait, pain and perception of the prosthesis.

Detailed description

The study is divided into three phases. The initial phase lasts 6 to 8 weeks for each subject. For subjects of group 2 the length of the initial phase depends on the progression of the re-innervation. The initial phase ends, when the subject can perceive the tactile stimulate at the re-innervated area of the skin. During the initial phase, all subjects get a new prosthesis. To minimize the adjusting to the new prosthesis only a new socket, which houses the vibro-tactile Feedback system, is fabricated and the old prosthetic food is re-used. After a period of 3 weeks minimum, where the subjects use the new prosthesis, a gait analysis and an assessment of the sensitivity of the skin at the stump are performed. Subsequently the intervention phase starts and the vibro-tactile feedback system is activated. For a period of 6 months the subjects use the new prostheses with the integrated vibro-tactile feedback system in daily living. After 2 and 4 months, the subjects visit the study site for an assessment of the sensitivity of the skin. After 6 months a second gait analysis and an other assessment of the sensitivity of the skin a the stump are performed. Afterwards the vibro-tactile feedback-system is disabled. During the observing phase the subjects use the prosthesis with the disabled vibro-tactile feedback system for 4 months. During all three phases the subjects answer the questionnaires every 2 months.

Interventions

DEVICEVibro-tactile Feedback

The device measures the force between the prosthetic food and the ground. With this signals, vibratators are triggered. The vibrators are housed by the prosthetic socket and stimulate the stump.

Sponsors

University of Applied Sciences Upper Austria
CollaboratorOTHER
Agnes Sturma
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* unilateral trans-tibial amputation * uses a prostheses already for more than 1 year * sufficient touch sensitivity at the stump * unimpaired contralateral lower extremity

Exclusion criteria

* psychiatric disorder * cognitive restrictions * pregnant or breast feeding women

Design outcomes

Primary

MeasureTime frameDescription
Trinity Amputation and Prosthesis Experience Scales-Revised (TAPES-R)1 yearThe Trinity Amputation and Prosthesis Experience Scales-Revised (TAPES-R) is a multidimensional instrument designed to examine the psychosocial processes involved in adjusting to amputation and a prosthesis. TAPES consists of 9 subscales, with possible scores depending on the single subscale. The range is from 0-12 to 0-25 (depending on the number of items and answer possibilities).

Secondary

MeasureTime frameDescription
Pain Visual analoge scale (VAS)1 yearThe pain is measured with a Visual analoge scale form 0 to 10. O indicates no pain, while 10 is the worst pain the person can imagine.
Number of falls within the last two months1 YearSubjects report the number a falls within the last two months.
Fall Efficacy Scale International Version (FES-I)1 yearThe Fall Efficacy Scale International Version (FES-I) is a questionaire that assesses the fear of falling. Scores can range from 16-64, with a higher score indicating a higher fear of falling.
two point discrimination6 monthsthe two point discrimination (in mm) at the skin of the stump is assessed
touch perception threshold6 monthsthe touch percertion at the skin of the stump is assessed with mono filaments
Gait parameters6 monthsTwo gait analysis are performed with a 3D video-based marker system. Standard gait parameters (as cardence, speed, step length and weight) as well as kinematic and kinetic parameters are calculated.

Contacts

Primary ContactAgnes Sturma, MSc
agnes.sturma@meduniwien.ac.at+43140400
Backup ContactOskar Aszmann
oskar.aszmann@meduniwien.ac.at+43140400

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026