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Whole Body Vibration in Children With Cerebral Palsy (CP)

K

Kutahya Health Sciences University

Status

Completed

Conditions

Spastic
Cerebral Palsy

Treatments

Other: whole body vibration training program
Other: conventional physiotherapy program

Study type

Interventional

Funder types

Other

Identifiers

NCT05636241
WBWinCP

Details and patient eligibility

About

Some positive effects of whole body vibration applications in reducing spasticity, improving walking ability, and increasing walking speed have been reported in children with CP, but the evidence is not strong enough. Therefore, this study was planned to evaluate the effect of whole body vibration treatment on spasticity, gait, balance, and motor performance in children with spastic CP. This study hypothesis that whole body vibration provides an additive improvement on spasticity, balance, gait and motor performance.

Full description

Participants will be evaluate at baseline, after the conventional physiotherapy program, and after whole body vibration training program. During this period, the participants who were recruited whole body vibration training program, whole body vibration will be applied in addition to conventional physiotherapy sessions comprised 45 min, 2 days a week, during 8 week.

Enrollment

13 patients

Sex

All

Ages

6 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children diagnosed with spastic diplegic CP in GMFCS levels I and II, CFCS level I and MACS levels I and II
  • Aged 6-17 years
  • Ability to cooperate with the evaluations
  • Walking independently with or without an orthosis (without any support)

Exclusion criteria

  • Having a recent injury affecting the lower extremities
  • Having undergone any surgery or Botulinuim Toxin application within the last six months
  • Having severe cardiopulmonary or systemic problems
  • Having uncontrolled seizures, visual or hearing problems preventing the evaluations

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

13 participants in 2 patient groups

control group
Active Comparator group
Description:
The participants in the control group will be attended to conventional physiotherapy program.
Treatment:
Other: conventional physiotherapy program
study group
Experimental group
Description:
The participants in the study group will be attended to whole body vibration training program.
Treatment:
Other: whole body vibration training program

Trial contacts and locations

1

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Central trial contact

Eda Özge OKUR; İsmail OKUR

Data sourced from clinicaltrials.gov

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