Spinal Mobility in Children With Cerebral Palsy: NDT-Bobath and Exergaming

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-18
SponsorWroclaw University of Health and Sport Sciences

About this trial

The purpose of this study is to evaluate changes in spinal mobility in the cervical, thoracic, and lumbar regions in children with cerebral palsy aged 10-15 years. The study will compare outcomes between standard NDT-Bobath therapy supplemented with exergaming in a sitting position and exergaming in a standing position. Postural stability, body composition, and functional parameters will also be assessed.

Participants will complete a socio-medical questionnaire and undergo baseline measurements of spinal mobility, cervical range of motion, postural stability (using Podoscan and Zebris platform), body height, and body composition (using SECA stadiometer and Tanita bioimpedance analyzer).

The intervention will last 3 months and include twice-weekly 60-minute therapy sessions. Group I will receive NDT-Bobath therapy supplemented with exergaming in a sitting position, while Group II will receive NDT-Bobath therapy with exergaming in a standing position.

After the intervention, participants will undergo post-intervention measurements and a follow-up evaluation three months later to assess the persistence of any changes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Written informed consent from parents/guardians and the child (if capable)

GMFCS levels I-III (mild to moderate motor limitations)

Ability to maintain standing position

Ability to follow instructions and perform exercises

Disqualifiers

GMFCS levels IV-V

Orthopedic surgery within the past 12 months

Seizure episodes within the past 6 months

Cognitive or behavioral impairments preventing cooperation

Trial design

Design model

Parallel

Treatments tested in this trial

  • NDT-Bobath Therapy

    Other intervention

    Standard NDT-Bobath neurodevelopmental therapy focusing on normalization of muscle tone in the pelvic and shoulder girdle, enhancement of central trunk stability including rotational control, and promotion of symmetrical posture and controlled movements according to NDT principles (facilitation, stimulation, communication). Dosage - 60-minute sessions, twice weekly, for 3 months.

  • Sitting Exergaming

    Other intervention

    Exergaming performed in a seated position using Kinect Therapy-Based Exergames. Participants sit on an adjustable chair with hips, knees, and ankles flexed at 90°. Exercises involve safe, non-impact, visually engaging three-dimensional trunk and limb movements, personalized to the child's functional level. Movements are synchronized with the MyoMotion system for monitoring. Dosage - 60-minute sessions, twice weekly, for 3 months (as part of combined therapy).

  • Standing Exergaming

    Other intervention

    Exergaming performed in a standing position using Kinect Therapy-Based Exergames, promoting weight-bearing and functional trunk and limb control. Exercises involve safe, visually engaging three-dimensional movements, personalized to the child's functional abilities. Movements are synchronized with the MyoMotion system for real-time monitoring. Dosage - 60-minute sessions, twice weekly, for 3 months (as part of combined therapy).

Treatment groups

42 Participants
are divided into 2 treatment groups
Group A: NDT-Bobath + Sitting ExergamingExperimental treatment 2 interventions
Group B: NDT-Bobath + Standing ExergamingExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Cervical Spine Mobility

Change in active cervical spine range of motion in children with cerebral palsy aged 10-15 years, measured in sagittal, frontal, and transverse planes using the CROM device. Cervical flexion/extension, lateral flexion, and rotation are expressed in degrees.

Time frame
Baseline, post-intervention (3 months), follow-up (6 months)
2

Thoracic Spine Mobility

Change in thoracic spine mobility measured as active range of motion and trunk rotation using the MyoMotion system. Measurements are expressed in degrees and reflect thoracic flexion/extension, lateral flexion, and rotational movements.

Time frame
Baseline, post-intervention (3 months), follow-up (6 months)
3

Lumbar Spine Mobility

Change in lumbar spine mobility measured as active range of motion using the MyoMotion system. Lumbar flexion/extension, lateral flexion, and rotation are expressed in degrees.

Time frame
Baseline, post-intervention (3 months), follow-up (6 months)

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: