跳至主要内容
临床试验/NCT04132999
NCT04132999已完成不适用

Positive Airway Pressure for the Treatment of the Obstructive Sleep Apnea Syndrome in Children With Down Syndrome (Stage 2)

University of Miami6 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2021年3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
27
试验地点
6
主要终点
Efficacy of INT-PAP in promoting PAP adherence

研究概览

简要总结

Determine the efficacy of family-informed intervention (INT) vs standard clinical care over a period of twelve months in children with obstructive sleep apnea and Down Syndrome.

详细描述

Evaluate the effect of PAP adherence on quality of life, neurobehavioral, and healthcare utilization in children with DS and OSAS. It is being hypothesized that, irrespective of study arm, increased PAP adherence will be associated with better quality of life, neurobehavioral, and healthcare utilization outcomes.

Evaluate the effect of PAP adherence in children with DS and OSAS on patient-centered outcomes and family-relevant outcomes identified during the R61 phase of this research. It is being hypothesized that irrespective of study arm, increased PAP adherence will be associated with better patient-centered outcomes, and family-relevant outcomes identified during the first year of this research.

Determine the efficacy of INT vs. CON in promoting PAP adherence. It is being hypothesized that that children receiving INT will show significantly increased objectively-measured PAP adherence at 6 months compared with those receiving CON (Aim 4A). As a secondary aim (4B), it will be evaluated whether the improved adherence is maintained over 12 months. It is being hypothesized that participants initially randomized to the INT arm will have better adherence at 12 months compared to those in the CON arm.

Use mixed methods during the randomized controlled trial to identify family perceptions, such as empowerment and self-efficacy, regarding PAP use in youth with OSAS and DS. It is being hypothesized that INT-PAP will be associated with more positive perceptions compared to CON.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
6 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical referral for PAP initiation to treat OSAS
  • Ages 6-18 years
  • Children are able to cooperate with testing
  • Have not used PAP for the past 3 years prior to enrollment

排除标准

  • Major illnesses, such as leukemia or severe cyanotic congenital heart disease listed for cardiac transplant.
  • Family planning to move out of the city within the next year
  • Children in foster care
  • Child with previously treated with PAP
  • Caregivers who do not speak English well enough to complete behavioral and performance measures.

研究组 & 干预措施

Family-informed intervention (INT)

Active Comparator

Multiple face-to-face visits, telephone calls and-person visits with the PAP psychologist and team.

干预措施: Family-informed intervention (Behavioral)

Standard Clinical Care

Active Comparator

Support which is given as part of the standard clinical care for patients who are currently prescribed PAP.

干预措施: Standard Clinical Care (Behavioral)

结局指标

主要结局

Efficacy of INT-PAP in promoting PAP adherence

时间窗: 6 months, and 12 months

Adherence to PAP expressed as percentage of nights used, and minutes of usage on nights used.

Efficacy of CON in promoting PAP adherence

时间窗: 6 months, and 12 months

Adherence to PAP expressed as percentage of nights used, and minutes of usage on nights used.

Effect of PAP adherence on quality of life and neurobehavioral outcomes

时间窗: Baseline, 6 months, and 12 months

PedsQL score and measures of executive functioning will be compared in the 2 groups. PedsQL is a 5-point scale ranging from 0-4 (0 = Never, 4 = Always).

Effect of PAP adherence in children with DS and OSAS on patient-centered outcomes and family-relevant outcomes identified during the R61 phase of this research

时间窗: Baseline, 6 months, and 12 months

Patient-centered outcomes and family-relevant outcomes - identified during the R61 phase of the study (Stage 1) - will be compared between the intervention and control groups. These are qualitative measures, and require interviews and further analysis to be established.

次要结局

  • Change in Behavior Rating Inventory of Executive Function, Second Edition (BRIEF-2) Parent Report Score(Baseline, 6 months, and 12 months)

研究者

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

Ignacio Tapia

Associate Professor of Pediatrics

University of Miami

研究点 (6)

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