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临床试验/NCT04198038
NCT04198038已完成不适用

A Pilot Study to Evaluate the Feasibility of Family-Centered Songwriting in Pediatric Palliative Care

Vanderbilt University1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2020年3月11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
25
试验地点
1
主要终点
Intervention feasibility and recruitment log

研究概览

简要总结

This study evaluates the feasibility and efficacy of a family-centered songwriting intervention for cognitively-impaired children referred to a palliative care service.

详细描述

Music-based interventions have previously been shown to reduce psychological distress in children with life-threatening conditions. However, children with cognitive impairment are frequently excluded from these studies. Our study will evaluate the efficacy a family-centered songwriting intervention for the following outcomes: child psychological and physical symptoms, parent psychological distress, and family environment.

Following recruitment, parent-child dyads will undergo 4 sessions with a licensed music therapist (anticipated to last 1 hour each). During these sessions, families and their children will select a song and engage in a songwriting process which includes various physiologic sounds from the child (i.e. heart rate, breathing). At the conclusion of these four sessions, a music DVD will be produced and delivered to the family.

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

年龄范围
7 Years 至 17 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •children ages 7-17 years
  • •cognitive impairment (T-score of 40 or below on the PROMIS Parent-Proxy Cognitive Function)
  • •receiving palliative/complex care
  • •progressively declining disease
  • •ability to hear.
  • •parents 18 years of age and older
  • •parent without cognitive impairment
  • •parent able to speak/understand English

排除标准

  • 未提供

研究组 & 干预措施

cognitively impaired children

Experimental

This is a single-group study; all participants will be offered the songwriting intervention.

干预措施: Songwriting with licensed music therapist (Behavioral)

结局指标

主要结局

Intervention feasibility and recruitment log

时间窗: throughout study completion, an average of 1 year

Number of enrolled participants who complete all phases of study

次要结局

  • Parent Proxy Physical Stress Experiences(Will be obtained at Time 1 (baseline, at recruitment) and at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline))
  • Parent Proxy Sleep Disturbance Short Form(Will be obtained at Time 1 (baseline, at recruitment) and at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline))
  • Parent Proxy Anxiety(Will be obtained at Time 1 (baseline, at recruitment) and at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline))
  • Parent Anxiety(Will be obtained at Time 1 (baseline, at recruitment), at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline), and at Time 3 (one month following death of child, if death of child occurs during study period.))
  • Parent Proxy Depressive Symptoms(Will be obtained at Time 1 (baseline, at recruitment) and at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline))
  • Parent Sleep Disturbance(Will be obtained at Time 1 (baseline, at recruitment), at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline), and at Time 3 (one month following death of child, if death of child occurs during study period.))
  • Change in cortisol levels(Before and after each songwriting intervention session throughout study completion, an average of 1 year)
  • Parental Perceived Stress (NIH Toolbox)(Will be obtained at Time 1 (baseline, at recruitment), at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline), and at Time 3 (one month following death of child, if death of child occurs during study period.))
  • Parent Satisfaction(Will be obtained at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline), and at Time 3 (one month following death of child, if death of child occurs during study period.))
  • Parent Proxy Psychological Stress Experiences(Will be obtained at Time 1 (baseline, at recruitment) and at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline))
  • Family Relationships(Will be obtained at Time 1 (baseline, at recruitment) and at Time 2 (at completion of intervention, estimated at 3-4weeks following baseline))

研究者

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

Terrah Akard

Associate Professor

Vanderbilt University

研究点 (1)

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