Last reviewed · How we verify

NCT06900322

Impacts of a Physical Therapy Protocol on Motor Function in Children With Congenital Zika Syndrome

Completed NA Last updated 28 March 2025
What this trial tests

NA trial testing Experimental Group (stimuli and handling; physical therapy [PediaSuit]) in Congenital Zika Syndrome in 16 participants. Completed in 8 May 2018.

Timeline
15 January 2018
Primary endpoint
8 May 2018
8 May 2018

Quick facts

Lead sponsorGabriela Lopes Gama
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment16
Start date15 January 2018
Primary completion8 May 2018
Estimated completion8 May 2018
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Gabriela Lopes Gama

Who can join

Eligibility, any sex, with Congenital Zika Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study aims to evaluate the effects of a specialized physiotherapy protocol aimed at the motor function of children with Congenital Zika Virus Syndrome. First, participants' anthropometric parameters (weight and length) and motor functions were assessed. After that participant were splited in two groups: Experimental group that uunderwent a one-hour daily protocol (5 times a week) of stimuli and handling based on the neuroevolutionary concept, and motor physical therapy with therapeutic garments (PediaSuit). On the other hand, the control group (CG) kept the therapeutic routine (conventional physical therapy).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06900322.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing