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Clinical Trials/NCT06398756
NCT06398756
Recruiting
Not Applicable

The Impact of Aquatic Therapy on Walking, Balance Functions, and Quality of Life in Children With Cerebral Palsy

Ankara City Hospital Bilkent1 site in 1 country34 target enrollmentSeptember 1, 2023
ConditionsCerebral Palsy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Palsy
Sponsor
Ankara City Hospital Bilkent
Enrollment
34
Locations
1
Primary Endpoint
Modified Ashworth Scale (MAS)
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The purpose of the study is to contribute to the rehabilitation program by comparing the effects of traditional rehabilitation methods and aquatherapy given in addition to these methods in patients with cerebral palsy. If the superiority of the rehabilitation program including aquatherapy is demonstrated, evidence will be provided for its more widespread use.

Detailed Description

The participants will be divided into two groups as the study group and the control group. The study group will receive an aquatherapy rehabilitation program in addition to the conventional rehabilitation program, while the control group will only receive the conventional rehabilitation program.

Registry
clinicaltrials.gov
Start Date
September 1, 2023
End Date
September 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Emel TURGUT VARAN

medical doctor

Ankara City Hospital Bilkent

Eligibility Criteria

Inclusion Criteria

  • Having a diagnosis of Hemiplegic Type or Diplegic Type Cerebral Palsy
  • Being between the ages of 3 and 16
  • Being at GMFCS levels I, II, and III
  • Having sufficient cognitive abilities such as understanding simple instructions, following them, and performing requested tasks
  • Parents and patients aged ≥ 9 agreeing to participate in the research

Exclusion Criteria

  • Experiencing uncontrolled seizures
  • Having serious learning difficulties, behavioral problems, skin lesions, visual and/or hearing impairments that could affect function and participation
  • Active infection
  • Incontinence

Outcomes

Primary Outcomes

Modified Ashworth Scale (MAS)

Time Frame: baseline, after 1 month and 3 month changes.

MAS 0: No increase in tone MAS 1: Minimal resistance or a catch and release at the end of the range of motion MAS 1+: Slight increase in tone, with minimal resistance felt in less than half of the range of motion MAS 2: Increased tone throughout most of the range of motion, but the joint can be easily moved MAS 3: Marked increase in tone, making passive movement difficult MAS 4: Rigidity in flexion or extension of the affected part

Gross Motor Function Measurement

Time Frame: baseline, after 1 month and 3 month changes.

The Gross Motor Function Measurement (GMFM) is an assessment method used to determine the motor development level of children with cerebral palsy. Its purpose is to measure not just the quality of motor performance, but rather how much of the movement the child has accomplished.

Secondary Outcomes

  • Pediatric Balance Scale(baseline, after 1 month and 3 month changes.)
  • The Functional Reach Test(baseline, after 1 month and 3 month changes.)

Study Sites (1)

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