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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04328168
Other study ID # 2016/442
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 15, 2016
Est. completion date January 15, 2017

Study information

Verified date March 2020
Source Kayseri Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A total of 28 patients who were followed-up in our clinic and received botulinum toxin injection of lower extremities in the last month were randomized to two groups in the study. Group 1 received conventional physiotherapy and Group 2 received robot-assisted gait training. The treatment period was 30 min/day, five sessions in a week, 15 sessions in total, for both groups. The study population was evaluated using range of joint motion evaluation chart, the Modified Ashworth Scale, The Gross Motor Function Classification System, The Berg Balance Scale, the functional independence measure for children, and the Edinburgh Visual Gait Score


Description:

A total of 28 patients who were followed-up in our clinic and received botulinum toxin injection of lower extremities in the last month were randomized to two groups in the study. Group 1 received conventional physiotherapy and Group 2 received robot-assisted gait training. The treatment period was 30 min/day, five sessions in a week, 15 sessions in total, for both groups. The study population was evaluated using range of joint motion evaluation chart, the Modified Ashworth Scale, The Gross Motor Function Classification System, The Berg Balance Scale, the functional independence measure for children, and the Edinburgh Visual Gait Score.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date January 15, 2017
Est. primary completion date October 15, 2016
Accepts healthy volunteers No
Gender All
Age group 7 Years to 10 Years
Eligibility Inclusion Criteria:

- Aged 4>, <16 with CP diagnosis

- Walking diffculties due to the spasticity of lower extremities,

- Level I-IV on the Gross Motor Function Classification System.

Exclusion Criteria:

- MAS Level IV spasticity, contractures, or rigidity in the lower extremities,

- A limb length inequality of >2 cm,

- Hypotonic CP,

- Having drug-related refractory epilepsy,

- Undergoing intrathecal baclofen pump surgery,

- Surgical interventions in the lower extremities in the last year,

- Scoliosis angle of >30°,

- Complicated osteoporosis (nontraumatic fracture...),

- Cardiovascular instability,

- GMFCS Level V,

- Metabolic disorder, genetic disease, neurodegenerative and neuromuscular diseases.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ROM exercises, stretching, positioning, gait training

by two physiotherapist under the supervision of a doctor


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kayseri Education and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary The Gross Motor Function Classification System (GMFCS) The Gross Motor Function Classification System or GMFCS is a 5 level clinical classification system that describes the gross motor function of people with cerebral palsy on the basis of self-initiated movement abilities. 3 weeks
Primary The Edinburgh Visual Gait Scale (EVGS) The Edinburgh visual gait score is an evaluative tool that uses software and video cameras to provide 3D video gait analysis as well as onscreen drawing and measurement tools to evaluate each portion of gait. The software will then generate a EVGS report, with illustrative images from the video if desired, in PDF format. 3 weeks
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