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临床试验/NCT03677752
NCT03677752已完成不适用

Guided Participation to Positioning (GP_Posit) Intervention for Mothers of Preterm Infants in the Neonatal Intensive Care Unit for Maternal Sensitivity and Infant's Neurodevelopment: Randomized Pilot Trial

St. Justine's Hospital1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年8月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
1
主要终点
Content analysis of acceptability questionnaires

研究概览

简要总结

The aim of this study is to evaluate the acceptability, feasibility and preliminary effects a GP_Posit intervention. GP_Posit is an intervention where mothers will learn how to participated in their preterm infant's care and positioning while being guided by a nurse. Preliminary effects will be estimated on maternal sensitivity, stress and anxiety as well as preterm infant's neurodevelopment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •This study will recruit mother-infant dyads.
  • •Inclusion Criteria for mothers:
  • •Understand, write and read French and/or English
  • •Are 18 years or older

排除标准

  • •for mothers:
  • •Use drugs
  • •Have an instable mental health
  • •Give their newborn infant for adoption
  • •Inclusion Criteria for preterm infants:
  • •Are born at 27 0/7 et 31 6/7 weeks of gestation
  • •Are hospitalized in the NICU for at least 4 weeks
  • •Exclusion Criteria for preterm infants:
  • •Require surgery
  • •Have intraventricular haemorrhage (IVH) > grade 2
  • •Have congenital malformations

研究组 & 干预措施

GP_Posit

Experimental

Participants allocated to this arm will receive the GP_Posit intervention.

干预措施: GP_Posit (Other)

Control

No Intervention

Participants in the control arm will receive usual care.

结局指标

主要结局

Content analysis of acceptability questionnaires

时间窗: When the infant reaches 36 weeks of gestational age (after the intervention that finished at 35 weeks of gestational age; before NICU discharge)

Mothers' answers to acceptability questionnaires will be analyzed. This is a questionnaire built by the research team aimed at collecting narrative data regarding mother's acceptability of the intervention. Elements such as acceptability of the length of the intervention, frequency of encounters, etc. will be assessed.

Compliance to the protocole

时间窗: Through study completion, an average of 1 1/2 year.

Compliance to the protocole to assess feasibility of the intervention GP_Posit and protocol. Research team will document aspects regarding % of recruitment, % of intervention delivered as planned, etc. through study completion. A threshold of 80% will be used to determine feasibility of the protocole elements.

次要结局

  • Parental beliefs about preterm infant and parental role(At entry in the study and when the infant reaches 36 weeks of gestational age (after the intervention that finished at 35 weeks of gestational age; before NICU discharge))
  • General movement assessment (GMA)(When the infant reaches 36 weeks of gestational age (after the intervention that finished at 35 weeks of gestational age; before NICU discharge))
  • Electroencephalogram (EEG)(At entry in the study and when the infant reaches 36 weeks of gestational age (after the intervention that finished at 35 weeks of gestational age; before NICU discharge))
  • Mother-Infant interaction(When the infant reaches 36 weeks of gestational age (after the intervention; before NICU discharge))

研究者

发起方
St. Justine's Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Andréane Lavallée

Student

St. Justine's Hospital

研究点 (1)

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