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临床试验/NCT05899998
NCT05899998进行中(未招募)不适用

Bright IDEAS for Pediatric Palliative Care: A Problem-Solving Skills Intervention to Empower Parent Resilience

Children's Hospital Los Angeles2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年8月8日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
40
试验地点
2
主要终点
Feasibility of Bright IDEAS for parents

研究概览

简要总结

The goal of this or clinical trial is to test in the feasibility, acceptability and preliminary efficacy of the bright IDEAS problem solving skills training for parents of children in palliative care. The main questions it aims to answer are:

  • Is bright IDEAS problem solving skills training feasible and acceptable for parents of children referred to pediatric palliative care?
  • Does bright IDEAS reduce psychological distress in parents compared to parents receiving standard palliative care support?

Participants will:

  • Participate in 6-8 sessions of the bright IDEAS program.
  • Complete self report measures of psychological distress and well being.

If there is a comparison group: Researchers will compare bright IDEAS to standard palliative care support.

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 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Parents or legal guardians of male and female children (ages 0-21) of any race or ethnicity and of any underlying medical diagnosis
  • Child received at least one consult from the Comfort and Palliative Care team within the past month
  • One parent or primary caregiver per child
  • Able to speak, read, and write English or Spanish, and give informed consent

排除标准

  • Parent age less than 18 years old
  • Concurrent enrollment on another research study testing psychoeducational interventions for parents and/or patients
  • Child has an estimated life expectancy of less than 4 months at time of study recruitment
  • Inclusion Criteria:
  • Children 8-17 years of age whose primary caregiver has consented to participate
  • Able to read and write English or Spanish and assent
  • Exclusion Criteria:
  • Parent refusal to participate

结局指标

主要结局

Feasibility of Bright IDEAS for parents

时间窗: Baseline to 12 weeks

Percent eligible participants who consent/assent to participate and Number of sessions completed by enrolled participants.

Parent Problem-Solving skills

时间窗: Baseline to 16 weeks

Social Problem-Solving Inventory-Revised Short Form. This is a a 25-item self-report instrument that measures five dimensions of problem-solving (positive problem orientation, negative problem orientation, rational problem-solving style, impulsive/carelessness style, and avoidant style) using a five-point Likert scale (0 = "Not at All True of Me" to 4 = "Extremely True of Me"). Summary scores for each subscale as well as a Total Raw Score range from 0-20. Higher scores indicate better self-reported problem-solving skills.

Depression symptoms

时间窗: Baseline to 16 weeks

PROMIS® Depression Short Form-v 1.0 8a. This self-report measure includes includes 8 items on which participants respond using a 5-point scale (1 = "Never" to 5 = "Always"). Total raw scores range from 8-40 and are converted to standardized T-scores with a mean of 50 and standard deviation of 10. Higher scores indicate higher levels of depressive symptoms.

Traumatic stress symptoms

时间窗: Baseline to 16 weeks

Abbreviated Posttraumatic Checklist -Civilian Version (PCL-6). This is a 6-item self-report screening measure empirically derived from the PCL-C, consisting of the most highly responsive items from each of the reexperiencing, avoidance, and hyperarousal symptom domains of the PCL-C and has previously been used with parents of children with serious illness. The PCL-6 uses a five-point Likert scale (0 = "Not at all" to 5 = "Extremely"), with total scores ranging from 6-30. Higher scores indicate higher levels of traumatic stress symptoms.

Anxiety symptoms

时间窗: Baseline to 16 weeks

PROMIS® Anxiety Short Form-v1.0 8a. This self-report measure includes includes 8 items on which participants respond using a 5-point scale (1 = "Never" to 5 = "Always"). Total raw scores range from 8-40 and are converted to standardized T-scores with a mean of 50 and standard deviation of 10. Higher scores indicate higher levels of anxiety.

次要结局

  • Child Quality of Life (QoL) Parent Proxy 0-7 years old(Baseline to 16 weeks)
  • Parent Wellbeing(Baseline to 16 weeks)
  • Child Quality of Life (QoL) Parent Proxy 8+ years old(Baseline to 16 weeks)
  • Child Quality of Life (QoL) Child Self-Report(Baseline to 16 weeks)

研究者

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

Bemis, Heather

Principal Investigator

Children's Hospital Los Angeles

研究点 (2)

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