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临床试验/NCT05835765
NCT05835765Unknown不适用

Use of Dynamic Elastometric Body in Preterm Newborns: A Prospective Pilot Study With a Medical Device

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2024年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
24
试验地点
1
主要终点
Modification or reduction of hyperexcitability syndrome with the use of Dynamic Elastometric Bodysuit

研究概览

简要总结

The goal of this prospective pilot study is to test the use of dynamic elastomeric body in a population of preterm newborns with hyperexcitability syndrome.

The main questions it aims to answer are:

  • To evaluate the effectiveness of the body in elasto-compressive material (FLEXA) in addition to standard care;
  • To evaluate how the use of dynamic elastomeric body promote postural containment, reduce hyperexcitability (tremor and crying), improve the organization of movement and reduce respiratory distress.

Participants will be given to routine clinical evaluations that are part of the standard of care of the premature infant admitted to Neonatology.

The clinical evaluation shall consist of:

  • Hammersmith neonatal neurological examination;
  • Neonatal Intensive Care Unit Network Neurobehavioural Scale (NNNS);
  • General Movement's (GM's)
  • Goal Attainment Scaling (GAS) Researchers will compare a study group that will be subjected to treatment with the body in elasto-compressive material and a control group without using the body in elasto-compressive material.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
8 Days 至 1 Month(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Signs of hyperexcitability such as tremors, sudden and chaotic movements, prevalent extensor tone, postural instability and/or neurovegetative phenomena;
  • •Low neurological risk, i.e., according to the protocols implemented in the standard clinical practice of the Neonatology unit, a cerebral ultrasound is performed for those born between 28-32 weeks of GA, and for those born before 28 weeks of GA, an MRI of the brain) from which it may derive;
  • •Cerebral ultrasound normal or with minor ultrasound findings such as grade 1 intraventricular hemorrhage (germinal matrix hemorrhage with intraventricular hemorrhage covering less than 10% of the ventricular area in the parasagittal window), or evidence of transient focal white matter hyperechogenicity.
  • •Issue of informed consent by the parent or legal guardian.

排除标准

  • •Neuroimaging findings of major brain lesions, such as evidence of grade 2 or greater intraventricular hemorrhage on cerebral ultrasonography (germinal matrix hemorrhage with intraventricular hemorrhage over 10% of the ventricular area in the parasagittal window/with periventricular hyperechogenicity ) or persistent hyperechogenicity for more than a week;
  • •Presence of: ongoing infectious states and/or sepsis, ostomy wearers, severe cardio-respiratory disorders at the time of enrolment; diagnosis of genetic or metabolic diseases; carriers of cerebral malformations; invasive or non-invasive respiratory assistance;
  • •Failure to issue informed consent by the parent or legal guardian.

研究组 & 干预措施

Dynamic Elastometric Body and neurological evaluation

Experimental

Use of dynamic elastometric body for one week and neurological evaluation before use of body, at 30 minutes after application, at one week after using the device and at 1th months since discharge

干预措施: Dynamic Elastometric Body in Preterm Newborns (Device)

Neurological evaluation

No Intervention

Neurological evaluation at enrollment, at one week after enrollment and at 1th months since discharge

结局指标

主要结局

Modification or reduction of hyperexcitability syndrome with the use of Dynamic Elastometric Bodysuit

时间窗: at one month from hospital discharge

Modification or reduction of hyperexcitability syndrome with use of Dynamic Elastometric Bodysuit in addition to standard care in terms of improvement of Goal Attainment Scaling (GAS) between the two groups. The GAS scale report a 5 level score between -2 ( worse score) to +2 (better score)

Modification or reduction of hyperexcitability syndrome with the use of Dynamic Elastometric Bodysuit

时间窗: baseline

Modification or reduction of hyperexcitability syndrome with use of Dynamic Elastometric Bodysuit in addition to standard care in terms of improvement of Goal Attainment Scaling (GAS) between the two groups. The GAS scale report a 5 level score between -2 ( worse score) to +2 (better score)

Modification or reduction of hyperexcitability syndrome with the use of Dynamic Elastometric Bodysuit

时间窗: One week of application of Dynamic Elastometric Body

Modification or reduction of hyperexcitability syndrome with use of Dynamic Elastometric Bodysuit in addition to standard care in terms of improvement of Goal Attainment Scaling (GAS) between the two groups. The GAS scale report a 5 level score between -2 ( worse score) to +2 (better score)

次要结局

  • Neurological Outcome with Hammersmith neonatal neurological examination (HNNE)(At one month from hospital discharge)
  • Neurobehavioural Outcome with NICU Network Neurobehavioural Scale (NNNS).(At one month from hospital discharge)
  • Neurological Outcome with "Prechtl's Assessment of General Movements (GMs)"(At 30 minutes from the use of Dynamic Elastometric Body)
  • Neurological Outcome with Hammersmith neonatal neurological examination (HNNE)(baseline)
  • Neurological Outcome with Hammersmith neonatal neurological examination (HNNE)(One week after the use of Dynamic Elastometric Body)
  • Neurobehavioural Outcome with NICU Network Neurobehavioural Scale (NNNS).(baseline)
  • Neurobehavioural Outcome with NICU Network Neurobehavioural Scale (NNNS).(One week after the use of Dynamic Elastometric Body)
  • Neurological Outcome with "Prechtl's Assessment of General Movements (GMs)"(baseline)
  • Neurological Outcome with "Prechtl's Assessment of General Movements (GMs)"(One week after the use of Dynamic Elastometric Body)
  • Neurological Outcome with "Prechtl's Assessment of General Movements (GMs)"(At one month from hospital discharge)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Romeo Domenico Marco

Assistant professor, Principal investigator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

研究点 (1)

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