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Not yet recruiting NCT07072533

Effect of Blood Flow Restriction With Aerobic Training on Chest Muscles in Diaplegic Cerebral Palsy

No phase Interventional Cerebral Palsy Spastic Diplegia

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
The protocol lists: blood flow restriction training.
Who it may be relevant to
Registry conditions: Cerebral Palsy Spastic Diplegia. Basic parameters: 12 years — 25 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 →

Overview

To evaluate the effect of blood flow restriction combined with aerobic training on chest muscle strength in individual with diaplegic cerebral palsy

Detailed description

combining blood flow restriction with aerobic training may enhance muscle function and endurance by increasing localized metabolic stress and systemic cardiovascular effects inducing muscular hypertrophy and strength gaining with low load training especially chest muscles which affected in individuals with diaplegic cerebral palsy.

Interventions

  • Other blood flow restriction training
    individual will do aerobic training .

Primary outcome measures

  • Chest muscle strength [Time frame: 3 months]
Secondary outcome measures (4)
  • pulmonary function tests [Time frame: 3 months]
  • sub-maximal aerobic capacity [Time frame: 3 months]
  • quality f life [Time frame: 3 months]
  • oxygen saturation and heart rate response [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

diaplegic cerebral palsy. GMFCS level I-III. medically stable.

Exclusion criteria

severe cognitive impairment. cardio respiratory contraindication. previous thoracic surgery or musculoskeletal deformities affecting chest.

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

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07072533 · SREC.PT.SUE(11)625

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗