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Not yet recruiting NCT07725627

Effect of Q Angle and BMI on Dynamic Balance in Spastic Diplegic Children

— Observational Diplegic Cerebral Palsy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Diplegic Cerebral Palsy. Basic parameters: 6 years — 10 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Effect of Quadriceps Angle and Body Mass Index on Dynamic Balance in Ambulatory Spastic Diplegic Children

Overview

The study aims to correlating q angel and BMI to dynamic balance in the diplegic children

Detailed description

Our study will be performed to detect if there is an effect of quadriceps angle on the dynamic balance of the ambulatory diplegic children, and also detect if there is and effect of body mass index on the dynamic balance of these children

Primary outcome measures

  • Dynamic balance [Time frame: 4 months]
Secondary outcome measures (2)
  • Q Angle [Time frame: 4 months]
  • BMi [Time frame: 4 months]

Eligibility criteria

Inclusion criteria

  • Ages between 6 to 10 years.
  • Children heights should be more thsn 1 meter.
  • Grade 1 or 1+ spasticity according to modified ashworth scale
  • Level 1 or 2 on gross motor function classification system.
  • All children are able to follow verbal commands.

Exclusion criteria

  • Children with epileptic fits.
  • Severe visual and auditory problems.
  • Fixed deformities of the lower extremities.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07725627 · P.T.REC/012/006098

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗