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Neonatal Brachial Plexus Palsy clinical trials

View clinical trials related to Neonatal Brachial Plexus Palsy.

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NCT ID: NCT04412603 Completed - Clinical trials for Neonatal Brachial Plexus Palsy

Emergent Therapies in OBP. Pilot Study

Start date: February 26, 2020
Phase: N/A
Study type: Interventional

Obstetric Brachial Palsy (OBP) produces functional limitations in the involvement of the affected upper limb within the child's natural environment. The therapeutic interventions of Conventional Mirror Therapy (MT) and Mirror Therapy Virtual Reality (VR) are aimed at the rehabilitation of the affected upper limb and the quality life improvement. To quantify the increase in the affected upper limb spontaneous use and the quality of life of children with upper OBP from 6-12 years, when They are treated with Conventional MT or Mirror Therapy VR applying specific protocol: 20 min/day in 4 weeks.

NCT ID: NCT04376372 Completed - Clinical trials for Neonatal Brachial Plexus Palsy

Forced Lefthandedness in Neonatal Brachial Plexus Palsy (NBPP) Children

NBPP
Start date: May 1, 2016
Phase:
Study type: Observational

The aim of the project is to assess the neurophysiological and functional consequences of forced lefthandedness in a population with right neonatal brachial plexus palsy (NBPP).

NCT ID: NCT03765034 Completed - Clinical trials for Neonatal Brachial Plexus Palsy

Constraint-induced Movement Therapy for Perinatal Brachial Plexus Injury

Start date: January 1, 2010
Phase: N/A
Study type: Interventional

This study evaluates the addition of constraint-induced movement therapy (CIMT) to usual care occupational therapy in children with perinatal brachial plexus injury. Participants are randomized to receive either the intervention (CIMT) or control first, then cross over to receive the other one.

NCT ID: NCT03440658 Completed - Clinical trials for Obstetrical Brachial Plexus Palsy

Deficits of Strength of the Rotator Muscles of the Shoulder in Children

ROTPOPB
Start date: July 1, 2018
Phase:
Study type: Observational

The purpose of this retrospective work is to study the consequences of obstetrical brachial plexus paralysis on the rotator muscles of the shoulder. First of all, the investigators want to study the reproducibility of the isometric contraction forces of the rotator muscles of the shoulder thanks to an isokinetic dynamometer. The investigatorsthen want to compare the measurements obtained from the paralyzed side compared to the healthy side. The preoperative MRI performed will be studied in search of amyotrophy. These data will be compared with those of the isokinetic assessment to identify children requiring muscle transfer of reinforcement of the external rotator muscles.

NCT ID: NCT01999465 Completed - Clinical trials for Neonatal Brachial Plexus Palsy

NMES Efficacy on Patients With NBPP

Start date: November 2013
Phase: N/A
Study type: Interventional

Neonatal Brachial Plexus Palsy (NBPP), characterized by weakness and sensory loss in the affected arm, results from damage in the prenatal period to the nerves extending from the spine to the arm. Proper stretching and exercise of the joints and affected arm from the time of diagnosis can greatly assist in the development of healthy movement of the limb. Additionally, neuromuscular electrical stimulation has been shown to be an effective treatment in other neural disorders and therefore its effectiveness in NBPP is worth studying. In the case of NBPP patients, the loss in normal arm function can be observed very early. Young patients will often neglect using the affected arm or modify motions to avoid the use of the biceps muscle, specifically in hand to mouth actions such as gripping a bottle or placing toys or other objects in the mouth. A goal of this study is to test the effectiveness of NMES on improving the biceps muscle Medical Research Council (MRC) strength and active range of motion (AROM). The subjects of this study are newborns between the ages of 3-9 months who are already a part of the University of Michigan Brachial Plexus program. Parents of the children will be trained to perform the neuromuscular electrical stimulation therapy at home using the EMPI Continuum unit for 30 minutes each day and monthly follow up appointments will be performed be the research occupational therapists throughout three month study period. Parents of the participants will complete a questionnaire before and during the study period to help analyze for confounders and gather data regarding parent compliance and NMES effectiveness. To detect the effectiveness of NMES, two cohort groups using standard units and sham units will be recruited and compare with data analysis. The investigators predict that the NMES will effectively improve the ability of the neonate to increase use of the affected arm, specifically in muscle strength biceps MRC score and AROM.