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临床试验/NCT04409301
NCT04409301已完成不适用

Distress in the Pediatric Oncology Setting: Intervention Versus Natural Adaptation - A Multi-Center Study

Emory University16 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2020年9月18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
160
试验地点
16
主要终点
Change in Parent Reported Patient Distress with Distress Thermometer

研究概览

简要总结

Children with cancer undergo many procedures as part of their treatment, and are often hospitalized or have frequent clinic visits, which can be distressing. Using robots or toys may be promising interventions as they provide elements of distraction therapy to children undergoing stressful and painful medical procedures. The purpose of this study is to see whether the use of a robotic toy called My Special Aflac Duck will reduce distress in children who have been diagnosed with cancer. This multi-center study will involve 20 children, ages 3-10, at each of 8 hospitals and their parent or guardian. There will be a total of 160 participants enrolled nationally.

详细描述

Annually in the US, over 12,500 children and adolescents are diagnosed with cancer. Youth with cancer undergo numerous procedures, clinic visits, and hospitalizations as part of their treatment and are often hospitalized or frequently come to clinic for procedures and treatment. These events can be distressing and can contribute to a range of negative emotional and/or psychological outcomes. In younger children, coping with distress and anxiety is mediated by their level of cognitive development and affective regulation. Child Life Specialists assist patients and their families during medical experiences by providing individualized educational and emotional support. Distraction techniques, usually performed by Child Life professionals, appear to be better suited to the cognitive abilities of young children, however, the degree to which distraction results in long-term reductions of child distress has not been well-established. Parent(s)/families are also important factors to consider since they are often active in day-to-day care of pediatric cancer patients. Studies have shown that parents have an active role in supporting and training their children during procedures and aiding in interventions and/or during evaluations.

Multisensory toys involving audiovisual, kinesthetic, and tactile senses, requiring a player's active cognitive, motor, and visual skills, have been utilized as an active distraction technique with the potential of reducing pain and anxiety. Robots are promising interventions as they provide elements of distraction to children undergoing stressful and painful medical procedures. In a previous feasibility study completed by the investigative team, results demonstrate high acceptability of My Special Aflac Duck (MSAD) as a device and as a method of distraction for children coping with treatment for pediatric cancer. In addition, the MSAD animatronic device was shown to provide a fun distraction and was used as a tool for expressing feelings for children with cancer in the hospital.

This is a multi-center efficacy trial coordinated through the Aflac Cancer and Blood Disorder Center at Children's Healthcare of Atlanta (CHOA). Hospitals with pediatric oncology departments will be recruited and will be responsible for the enrollment of patients to participate in this study. All participating hospitals will have dedicated Child Life services. Randomized assignment for this trial will be performed at the hospital level. Four hospitals will be assigned to have patients receive the My Special Aflac Duck (MSAD) animatronic device at study initiation and four hospitals will be assigned to not have patients receive MSAD during the study but will receive MSAD at the end of the study.

The study plans to enroll a total of 160 patients and their parent(s)/guardian(s). Within each hospital, 20 families will be recruited; 10 with children aged 3.00-6.99 years and 10 with children aged 7.00-10.99 years.

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
3 Years 至 10 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged 3.00-10.99 years
  • All cancer diagnoses
  • English or Spanish speaking (parent and child)

排除标准

  • Patients who receive surgery only will be excluded as they will not have follow-up visits at which to complete the questionnaires
  • Patients with cognitive or sensory deficits that would impact being able to interact with MSAD and/or complete questionnaires
  • Patients who receive chemotherapy entirely inpatient and never have appointments in the outpatient setting

研究组 & 干预措施

MSAD Intervention

Experimental

Children receiving cancer treatment in a hospital randomized to the My Special Aflac Duck (MSAD) intervention.

干预措施: My Special Aflac Duck (MSAD) (Other)

Control Group

Active Comparator

Children receiving cancer treatment in a hospital randomized to be a control hospital. Children in the control hospitals will receive the My Special Aflac Duck (MSAD) at the end of the intervention period.

干预措施: Standard of care control (Behavioral)

结局指标

主要结局

Change in Parent Reported Patient Distress with Distress Thermometer

时间窗: Baseline, Week 1

The Distress Thermometer instrument asks respondents to indicate how much distress they are experiencing on a scale from 0 to 10 where 0 = no distress and 10 = extreme distress. Parents will report how much medical setting distress that they observe their children experiencing.

次要结局

  • Change in Patient Distress with Distress Thermometer as Reported by Child Life Specialists(Baseline, Week 1, Month 1, Month 3)
  • Change in Parent Report of Pediatric Quality of Life Inventory (PedsQL) - Generic Score(Baseline, Week 1, Month 1, Month 3)
  • Change Parent Reported in PedsQL - Cancer Module Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Child Reported PROMIS - Psychological Stress Experiences Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Child Reported PROMIS - Positive Affect Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Parent Reported PROMIS - Pain Behavior Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Child-Reported Distress with Distress Thermometer(Baseline, Week 1, Month 1, Month 3)
  • Change in Child Reported PedsQL - Cancer Module Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Child Life Specialist Reported Common Terminology Criteria for Adverse Events (CTCAE) - Pain(Baseline, Week 1, Month 1, Month 3)
  • Child Life Specialist Reported Satisfaction with the MSAD Intervention(Baseline, Week 1, Month 1, Month 3)
  • Change in Parent Reported PROMIS - Positive Affect Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Child Life Specialist Reported Common Terminology Criteria for Adverse Events (CTCAE) - Anxiety(Baseline, Week 1, Month 1, Month 3)
  • Change in Parent Reported CTCAE - Depression Score(Baseline, Week 1, Month 1, Month 3)
  • Parent Reported Satisfaction with the MSAD Intervention(Baseline, Week 1, Month 1, Month 3)
  • Change in Brief Symptom Inventory 18 (BSI-18) Score(Baseline, Week 1, Month 1, Month 3)
  • Child Reported Satisfaction with the MSAD Intervention(Baseline, Week 1, Month 1, Month 3)
  • Parent Reported Patterns of Utilization of the MSAD Intervention(Baseline, Week 1, Month 1, Month 3)
  • Child Life Specialist Reported Patterns of Utilization of the MSAD Intervention(Baseline, Week 1, Month 1, Month 3)
  • Change in Parent Reported Patient-Reported Outcomes Measurement Information System (PROMIS) - Psychological Stress Experiences Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Child Life Specialist Reported CTCAE - Depression Score(Baseline, Week 1, Month 1, Month 3)
  • Change in Child Reported CTCAE - Depression Score(Baseline, Week 1, Month 1, Month 3)

研究者

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

Tamara Miller

Assistant Professor

Emory University

研究点 (16)

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