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Clinical trial of comparing the immediate effect of both conventional and neoprene modified polypropylene ankle foot orthosis on kinematic parameters of gait in people with foot drop syndrome

Clinical trial of Comparing the immediate effect of both conventional and neoprene modified polypropylene ankle foot orthosis on kinematic parameters of gait in people with foot drop syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015120116810N3
Enrollment
20
Registered
2016-05-05
Start date
2016-01-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

DROP FOOT. (Wrist or foot drop (acquired

Interventions

Intervention 1: Intervention group 1: drop foot people will walk while wearing modified neoprane orthose in their shoes on kistler force plate to predict the components of the kinetic and kinematic ga
Treatment - Other
Intervention Group 2:The Test Will Be Taken While They'll Be Wearing Solid AFO With Their Shoes.
Intervention Group 3: The Test Will Be Taken Barefoot
Intervention group 1: drop foot people will walk while wearing modified neoprane orthose in their shoes on kistler force plate to predict the components of the kinetic and kinematic gait . The test pr

Sponsors

Vice chancellor for research of Iran University Of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
90 Years to 66 Years

Inclusion criteria

Inclusion criteria: The main inclusion criteria were: participants, with a score of 0 or 1 ankle dorsiflexors which cause their foot to be dragged in swing phase, one-sided weaknessof ankle dorsiflexor muscles, flaccid paralysis of the lower extremities following traumatic nerve injury, aged 25 to 50 years, the ability to walk without assistive devices for a period of 2 min. The exclusion criteria were: any painfull pain in the body, existing an open wound in the areas covered by the orthosis, obvious deformity in the lower extremities, disinclination to do more tests.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ankle joint angle. Timepoint: Immediate effect. Method of measurement: Using Kistler force plate and motion analyzer system in degrees.;Knee joint angle. Timepoint: Immediate effect. Method of measurement: Using Kistler force plate and motion analyzer system in degrees.;Hip joint angle. Timepoint: Immediate effect. Method of measurement: Using Kistler force plate and motion analyzer system in degrees.

Secondary

MeasureTime frame
Step length. Timepoint: Immediate effect. Method of measurement: Using Kistler force plate in centimeters.;Stance during. Timepoint: Immediate effect. Method of measurement: Using Kistler force plate in second.;Swing during. Timepoint: Immediate effect. Method of measurement: Using Kistler force plate in second.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026