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Spastic Equinus - Comparison between the effects of various ankle foot orthosis concepts

Spastic Equinus - Comparison between the effects of various ankle foot orthosis concepts

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014696
Enrollment
86
Registered
2018-06-04
Start date
2018-06-04
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

G80.1 M21.62

Interventions

Group 1: Knee-ankle-foot orthoses, wearing time at night (Company Pohlig). Intervention for 12 weeks Group 2: Knee-ankle-foot orthoses, wearing time at night. Without adaptable knee part for daytime u

Sponsors

Förderverein rege e.v.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 14 Years

Inclusion criteria

Inclusion criteria: Children with spastic cerebral palsy, hemiplegic and diplegic, GMFCS-level I-II, age ranged from 4 to 14 years, non-rigid equinus (it is defined as tone on the modified Ashworth Scale (MAS) max. 3 and a lack of passive range of motion smaller than -10 degree dorsiflexion)

Exclusion criteria

Exclusion criteria: Inability to follow verbal instructions, previous surgery to the leg within 1 year, botulinum toxin injections within 6 months, leg length discrepancies more than 2 cm, lack of passive range of motion greater than -10 degree of knee flexion from neutral

Design outcomes

Primary

MeasureTime frame
3D gait analysis: landing angle - foot to floor. Measurement before and after treatment

Secondary

MeasureTime frame
1) 3D gait analysis: velocity, max. dorsiflexion in late stance, max. ankle moment, ankle power 2) Ultrasound: Muscle belly length, Muscle belly thickness, Fascicle length, Fascicle angle, Tendon length 3) Force of plantarflexors 4) Passive stiffness of plantarflexors 5) Wearing time (Orthotimer)

Countries

Germany

Contacts

Public ContactHarald Böhm

Behandlungszentrum Aschau, Ganglabor

h.boehm@bz-aschau.de+49 (0)8052-171-2016

Outcome results

None listed

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