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Fiability of a Telerehabilitation Programme Based on the Neurodevelopmental Treatment (NDT) Model on Gross Motor Function and Functional Performance in Children With Cerebral Palsy.

E

Escola Superior Saúde Fernando Pessoa

Status

Active, not recruiting

Conditions

Cerebral Palsy Children

Treatments

Other: neurodevelopmental treatment based on the Bobath concept
Other: neurodevelopmental treatment according to the Bobath concept

Study type

Interventional

Funder types

Other

Identifiers

NCT07394985
ESTUDO_PC_TELEREAB_01

Details and patient eligibility

About

Experimental study with a control group, developed with the aim of analyzing the impact of a telerehabilitation program based on the Neurodevelopmental Treatment (NDT) model on gross motor function and functional performance in children with cerebral palsy.

Full description

The sample consisted of 20 children divided into two equivalent groups: an experimental group (n = 10), which received the TND intervention program in a synchronous telerehabilitation format for six months, and a control group (n = 10), which maintained the usual care and clinical follow-up plan without additional structured intervention.

The children included had a clinical diagnosis of spastic cerebral palsy, aged between 6 months and 6 years, classified between levels I and IV of the Gross Motor Function Classification System (GMFCS).

The pre-intervention assessment was performed before the start of the program, and the post-intervention assessment took place after six months. The assessments included the GMFM-88, to measure gross motor function, and the CO-OP Performance Measure (COOPM), to assess caregivers' perceptions of performance and satisfaction.

Enrollment

20 patients

Sex

All

Ages

6 months to 6 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria Confirmed diagnosis of cerebral palsy; Age between 6 months and 6 years; Ability of the primary caregiver to actively participate in online sessions; Regular access to a device with a camera and internet connection.

Exclusion criteria Orthopaedic surgery or botulinum toxin application in the six months prior to the intervention; Presence of severe comorbidities (cardiorespiratory, cognitive, or sensory) that would limit participation;

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

Intervention Group
Experimental group
Description:
telerhabilitation intervention in accordance with neurodevelopmental treatment
Treatment:
Other: neurodevelopmental treatment based on the Bobath concept
Control Group
Experimental group
Description:
face-to-face intervention in accordance with neurodevelopmental treatment
Treatment:
Other: neurodevelopmental treatment according to the Bobath concept

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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