跳至主要内容
临床试验/NCT02559557
NCT02559557已完成不适用

Adaptation and Pilot-Testing a Parenting Intervention for Spanish-Speaking Parents of Children at Risk for Neurocognitive Late Effects

City of Hope Medical Center2 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2015年10月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
38
试验地点
2
主要终点
Feasibility, measured by the percentage of parents who complete the entire adapted skills-training parenting intervention

研究概览

简要总结

This pilot clinical trial studies a culturally adapted skills training and educational intervention in guiding parents of younger acute lymphoblastic leukemia (ALL) or acute myeloid leukemia (AML) survivors at risk for long-term attention and memory problems (late neurocognitive effects). ALL and AML treatments target the central nervous system and may put younger survivors at increased risk for late neurocognitive effects, which may lead to learning difficulties or behavior problems and poor health-related quality of life. Spanish-speaking parents of young ALL or AML survivors may not have access to the information, resources, or guidance to help their children through these difficulties. Adapting an existing parent-training program into Spanish may help teach Spanish-speaking parents effective ways to prevent or reduce learning and behavioral difficulties, which may improve the quality of life of parents and young ALL or AML survivors.

详细描述

PRIMARY OBJECTIVES:

I. To culturally modify and adapt an existing educational and skills-training intervention for use with Spanish-speaking parents of children with acute lymphoblastic leukemia (ALL) or with acute myeloid leukemia (AML).

II. To pilot the culturally-modified, parenting intervention with eligible families of children treated for ALL or AML in the Pediatrics department at City of Hope.

OUTLINE:

PHASE I (FOCUS GROUPS): Parents undergo a semi-structured interview with bilingual research assistants over 120 minutes. The content and purpose of the intervention is explained, and the focus group discussions elicit feedback on the intervention components and content of the sessions, and whether the material is culturally and linguistically appropriate. Following the focus group discussion, parents receive a copy of the educational handouts that they may choose to use with their child if they like.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • INCLUSION CRITERIA FOR FOCUS GROUPS (PHASE I)
  • Parents or adult primary caregiver (e.g., grandmother) of children ages 5 to 17 in treatment remission and has completed intensive therapy for ALL or AML
  • Parents of childhood cancer survivors who are now 18 years or older and who were previously treated for ALL or AML (do not need to live with the child)
  • One or both of the parents will self-identify as Hispanic/Latino, the primary participating parent will be either Spanish speaking, bilingual, or is bilingual but identifies their primary language as English and will live with the child
  • INCLUSION CRITERIA FOR PILOT-TESTING (PHASE II)
  • Parent/Caregiver: parents or adult primary caregiver (e.g., grandmother) of children treated for ALL or AML
  • Parent/Caregiver: one or both of the parents will self-identify as Hispanic/Latino, the primary participating parent will be either Spanish speaking, bilingual, or is bilingual but identifies their primary language as English and will live with the child
  • Child: child is in treatment remission and has completed intensive therapy
  • Child: child is age 5 to 17 years, 11 months
  • Child: child understands English

排除标准

  • EXCLUSION CRITERIA FOR FOCUS GROUPS (PHASE I)
  • Parents of ALL or AML survivors with a history of a major psychiatric condition that precludes participation (e.g., psychosis, severe depression, active substance abuse)
  • Existing history of severe cognitive impairment in the child as reported by the parents or documented in the child's City of Hope medical records
  • EXCLUSION CRITERIA FOR PILOT TESTING (PHASE II)
  • Parent/Caregiver: parents with a history of a major psychiatric condition that precludes participation (e.g., psychosis, severe depression, active substance abuse)
  • Child: survivors with a history of a major psychiatric condition that precludes participation (e.g., psychosis, severe depression, active substance abuse)
  • Child: existing history of severe cognitive impairment (intelligence quotient [IQ] =< 70) as reported by the parents or the child's City of Hope medical records, or by the child's performance score on the Wechsler Intelligence Scale for Children (WISC) Working Memory and Processing Speed index measures administered in this study

结局指标

主要结局

Feasibility, measured by the percentage of parents who complete the entire adapted skills-training parenting intervention

时间窗: After 6 sessions (up to 12 months)

Feasibility will be operationally defined as \> 75% of parents completing the intervention.

次要结局

  • Change in learning strategies as measured by the School Motivation and Learning Strategies Inventory(Baseline to up to 12 months)
  • Change in parent knowledge and efficacy, as measured by the Parent Knowledge, Beliefs, and Behaviors Questionnaire (PBQ)(Baseline to up to 12 months)
  • Change in child's school-related health-related quality of life (HRQOL) score as assessed by the Pediatric Quality of Life scale(Baseline to up to 12 months)
  • Parent satisfaction with the intervention as measured by the perceived benefits scale(Up to 12 months)

研究者

发起方
City of Hope Medical Center
申办方类型
Other
责任方
Sponsor

研究点 (2)

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