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临床试验/NCT02394899
NCT02394899已完成不适用

Integrating a Parenting Intervention With Routine Care to Improve Parental Psychosocial Functioning and Early Developmental Outcomes in Children With Sickle Cell Disease

The University of The West Indies1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2014年10月1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
入组人数
64
试验地点
1
主要终点
Infant's development quotient (Griffiths Developmental Scale)

研究概览

简要总结

There are all significant risk factors for poor early cognitive development and, as such, neurocognitive deficits have been demonstrated in pre-school children with sickle cell disease (SCD). This project assesses the efficacy of using an evidence-based early stimulation program, combined with components to help parents cope with stress, delivered during six routine monthly clinic visits to parents of children with sickle cell disease. It is hoped that this innovation will improve parental psychological outcomes, as well as child developmental outcomes.

详细描述

Children with sickle cell disease (SCD) are at risk of various complications, many of which arise suddenly and call on the problem solving skills of their parents. They are also at risk of neurocognitive delays; these may become evident during the pre-school years. Previous research by this group has demonstrated improved developmental outcomes after parental interventions incorporating play techniques in high risk and healthy pre-school children. The aim of the study is to determine usefulness in children with SCD of similar developmental interventions augmented by lessons in problem solving.

The study is a randomized controlled trial. Parents of all infants with Hb SS (homozygous sickle cell disease) or Sβ0 -thalassemia disease identified by newborn screening during the initial year of the study will be invited to participate. They will be randomized to intervention or control. Parental stress, infant's development and hemoglobin levels will be measured at recruitment and again after six months. The intervention will occur during monthly Penadur (intramuscular Benzathine Penicillin) visits and will include supervised play with their children using an inexpensive toy and participation in solving a problem which may arise as they parent their child with SCD. At the end of the study, all control dyads will also be given the toys used in the intervention. All parents will be given the results of their children's developmental assessments and appropriate referrals made if deficits are identified.

The study is minimal risk. Every effort will be made to maintain patient confidentiality. Respect for, and the maximum protection of the best interests of the research subjects will be maintained.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
6 Months 至 12 Months(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Infant has sickle cell disease: SS or Sβ0 thalassemia
  • •Attending Sickle Cell Unit, Jamaica for routine care

排除标准

  • 未提供

研究组 & 干预措施

Control

No Intervention

The control dyad will receive usual care.

Intervened

Experimental

Parents receive training in problem solving skills and play therapy with their infants.

干预措施: Play therapy (Behavioral)

Intervened

Experimental

Parents receive training in problem solving skills and play therapy with their infants.

干预措施: Problem solving skills (Other)

结局指标

主要结局

Infant's development quotient (Griffiths Developmental Scale)

时间窗: 6 months

Griffiths Developmental Scale

Parental stress, depression and coping (Pediatric Inventory for Parents; CES-D; Coping Health Inventory for parents)

时间窗: 6 months

Questionnaires to assess: Pediatric Inventory for Parents; CES-D; Coping Health Inventory for parents

Parental problem solving skills (Social Problem Solving Inventory)

时间窗: 6 months

Using Social Problem Solving Inventory: Questionnaires

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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