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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03038815
Other study ID # Stability Boots
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2017
Est. completion date December 31, 2017

Study information

Verified date November 2019
Source Institute for Biomechanics, ETH Zürich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

After an ankle injury like distorsions, fractures or arthrodeses, or congenital defects ankle support limit the range of motion in the joint, help pain relief, control loading of the injured tissues and promote recovery of a normal gait pattern. Gait analysis is applied in orthopedics, sport science and rehabilitation. Numerous measure systems and methods enable accurate analysis of human movement.

The study is set to describe and compare the gait analysis of two modifiable stability boots (Ortho® Tri-Phase and the VACOped®) on the standard walking parameters during two conditions (level and ramp walking) in healthy adults and draw comparisons with a control indoor shoe.


Description:

The participants are joining one session in the gait lab. Here the are measured during walking with normal shoes and two modifiable stability boots. The duration of a session is typically 3 hours.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 31, 2017
Est. primary completion date June 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- healthy

- 18-45 years old

- shoe size 5,6,9 or 10

Exclusion Criteria:

- injuries of the lower limbs

- previous surgeries on the lower limbs

- neuromuscular disorders

- restriction in gait capabilities

- current medical treatment

Study Design


Related Conditions & MeSH terms


Intervention

Device:
VACOped
restriction of ankle joint motion
Ortho Tri
restriction of ankle joint motion

Locations

Country Name City State
Switzerland Institute for Biomechanics ETH Zürich Zurich ZH

Sponsors (1)

Lead Sponsor Collaborator
Institute for Biomechanics, ETH Zürich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary ROM Ankle Joint Ankle joint motion ROM Sagittal left, during gait duration of a session is typically 3 hours
Secondary Symmetrie Index The symmetrie index, represents the % difference step length, index= 2*100*(step length left-step length right)/(step length left+step length right) This measure has no unit. 0 would represent a total symmetric gait. duration of a session is typically 3 hours