PAP for Children With DS and OSAS
Primary Purpose
Down Syndrome, Obstructive Sleep Apnea
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Family-informed intervention
Standard Clinical Care
Sponsored by
About this trial
This is an interventional treatment trial for Down Syndrome focused on measuring Down Syndrome, Obstructive Sleep Apnea, PAP, Positive Airway Pressure
Eligibility Criteria
Inclusion Criteria:
- Clinical referral for PAP initiation to treat OSAS
- Ages 6-18 years
- Children are able to cooperate with testing
- Naive to PAP treatment
Exclusion Criteria:
- 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.
Sites / Locations
- Cincinnati Children's Hospital Medical CenterRecruiting
- The Children's Hospital of PhiladelphiaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Family-informed intervention (INT)
Standard Clinical Care
Arm Description
Multiple face-to-face visits, telephone calls and-person visits with the PAP psychologist and team.
Support which is given as part of the standard clinical care for patients who are currently prescribed PAP.
Outcomes
Primary Outcome Measures
Effect of PAP adherence on quality of life and neurobehavioral outcomes
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).
Efficacy of INT-PAP in promoting PAP adherence
Adherence to PAP expressed as percentage of nights used, and minutes of usage on nights used.
Efficacy of CON in promoting PAP adherence
Adherence to PAP expressed as percentage of nights used, and minutes of usage on nights used.
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
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.
Secondary Outcome Measures
Full Information
NCT ID
NCT04132999
First Posted
October 10, 2019
Last Updated
February 10, 2023
Sponsor
Children's Hospital of Philadelphia
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI), Children's Hospital Medical Center, Cincinnati, University of Pennsylvania
1. Study Identification
Unique Protocol Identification Number
NCT04132999
Brief Title
PAP for Children With DS and OSAS
Official Title
Positive Airway Pressure for the Treatment of the Obstructive Sleep Apnea Syndrome in Children With Down Syndrome (Stage 2)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
September 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital of Philadelphia
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI), Children's Hospital Medical Center, Cincinnati, University of Pennsylvania
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Down Syndrome, Obstructive Sleep Apnea
Keywords
Down Syndrome, Obstructive Sleep Apnea, PAP, Positive Airway Pressure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
family-informed intervention (INT) vs standard clinical care (CON).
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
86 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Family-informed intervention (INT)
Arm Type
Active Comparator
Arm Description
Multiple face-to-face visits, telephone calls and-person visits with the PAP psychologist and team.
Arm Title
Standard Clinical Care
Arm Type
Active Comparator
Arm Description
Support which is given as part of the standard clinical care for patients who are currently prescribed PAP.
Intervention Type
Behavioral
Intervention Name(s)
Family-informed intervention
Intervention Description
Multiple face-to-face visits, telephone calls and-person visits with the PAP psychologist and team
Intervention Type
Behavioral
Intervention Name(s)
Standard Clinical Care
Intervention Description
Support which is given as part of the standard clinical care for patients who are currently prescribed PAP.
Primary Outcome Measure Information:
Title
Effect of PAP adherence on quality of life and neurobehavioral outcomes
Description
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).
Time Frame
Baseline, 6 months, and 12 months
Title
Efficacy of INT-PAP in promoting PAP adherence
Description
Adherence to PAP expressed as percentage of nights used, and minutes of usage on nights used.
Time Frame
6 months, and 12 months
Title
Efficacy of CON in promoting PAP adherence
Description
Adherence to PAP expressed as percentage of nights used, and minutes of usage on nights used.
Time Frame
6 months, and 12 months
Title
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
Description
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.
Time Frame
Baseline, 6 months, and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinical referral for PAP initiation to treat OSAS
Ages 6-18 years
Children are able to cooperate with testing
Naive to PAP treatment
Exclusion Criteria:
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.
Facility Information:
Facility Name
Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stacey Ishman, MD
Phone
513-636-4944
Email
stacey.ishman@cchmc.org
First Name & Middle Initial & Last Name & Degree
Suzanna Hicks
Phone
(513) 636-4944
Email
Suzanna.Hicks@cchmc.org
Facility Name
The Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ignacio E Tapia, MD
Phone
267-426-5842
Email
tapia@chop.edu
First Name & Middle Initial & Last Name & Degree
Ruth Bradford
Phone
(267) 426-5747
Email
bradford@chop.edu
12. IPD Sharing Statement
Plan to Share IPD
No
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PAP for Children With DS and OSAS
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