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Continuous Positive Airway Pressure (CPAP) After Adenotonsillectomy in Children

Primary Purpose

Sleep Apnea, Obstructive, Sleep Apnea Syndromes, Child Behavior Disorders

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CPAP treatment
No CPAP treatment
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Apnea, Obstructive focused on measuring polysomnography, child, continuous positive airway pressure, tonsillectomy, neuropsychological tests, cognition, sleepiness, behavior

Eligibility Criteria

5 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Children ages 5-12 years old,
  2. Scheduled for an adenotonsillectomy for treatment of sleep apnea,
  3. Child must provide assent, and
  4. Parent or legal guardian must be able to speak and read English, and agree to the study.

Exclusion Criteria:

  1. No siblings of children already enrolled in the study,
  2. Children who expect to have another surgery (in addition to AT) during the period of participation in this study,
  3. Neurological, psychiatric, or medical conditions, or social factors that may affect test results, prevent children from returning for required study visits, or interfere with the study treatment, or
  4. Certain medications that affect sleepiness or alertness, for example:

    • Stimulants (such as Ritalin, Adderall, or Concerta),
    • Sleep aides (such as Melatonin, Ambien, or Ativan), or
    • Sedating medicines (such as Benadryl, Klonopin, Xanax, or Valerian).

Sites / Locations

  • University of Michigan Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

CPAP treatment

No CPAP treatment

Arm Description

Children randomized to this arm will receive 6 months of CPAP (or BPAP) treatment, beginning at approximately 4 months after AT, in addition to standard of care. For analysis purposes those children who were non-adherent (CPAP use <4 hours per night) vs. adherent (CPAP use at least 4 hours per night) will be analyzed separately.

Children randomized to this comparison arm will not be treated with CPAP or BPAP, but will be followed for approximately 10 months after AT while receiving standard of care.

Outcomes

Primary Outcome Measures

Change in Behavioral Index After 6 Months of CPAP or No-CPAP
The sum of the T-scores of The Conners' Parent Rating Scales (CPRS-R:L, ADHD index) and the Child Behavior Checklist (CBCL, Attention Deficit/Hyperactivity Problems) are used to construct the primary study outcome measure Behavioral Index. Behavioral index is a T score (adjusted for age and gender) with a range of "<10" to ">90" - where higher scores mean worse behavior and lower scores mean better behavior, so a negative change score represents an improvement in behavior. T-scores with a mean of 50 and SD of 10 are computed.

Secondary Outcome Measures

Change in Cognition as Shown by NIH Toolbox Composite Score
Scores are reported as standardized scores with a mean of 100 and SD of 15. Minimum value 40 and Maximum value 160. Higher scores are better
Change in Sleepiness as Measured by Epworth Sleepiness Scale
Epworth Sleepiness Scale scores range from 0 to 24 where higher scores mean greater sleepiness.
Change in Sleepiness After AT as Measured by Multiple Sleep Latency Test (MSLT)
Multiple Sleep Latency Test (MSLT) is an objective measure of sleepiness determined by measure of brain waves and other physiological signals over a 30 minute period. This is measured for five 30 minute periods across the day and average latency to sleep for each participant across those times were used to calculate the mean sleep latency. The score is measured in how quickly one would fall asleep, measured in minutes, so a negative number of minutes in the change score means that participants fell asleep more quickly than previously.
Change in Quality of Life as Measured by Peds QL
Peds-QL is a quality of life symptom measurement with a score range of 0 to 100. Higher scores are better quality of life
CPAP Adherence as Measured by Number of Participants Who Used the CPAP Consistently.
CPAP adherence data will be downloaded from CPAP machines. It is defined for this study as using the CPAP machine for at least an average of 4 hours per night during the last 60 days of the assignment.

Full Information

First Posted
March 1, 2012
Last Updated
January 10, 2019
Sponsor
University of Michigan
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), Michigan Technological University
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1. Study Identification

Unique Protocol Identification Number
NCT01554527
Brief Title
Continuous Positive Airway Pressure (CPAP) After Adenotonsillectomy in Children
Official Title
Sleep-Disordered Breathing and CPAP After Adenotonsillectomy in Children
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
October 29, 2017 (Actual)
Study Completion Date
October 29, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), Michigan Technological University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Obstructive sleep-disordered breathing (SDB) affects 2-3% of children and may lead to problems with nighttime sleep and daytime behavior, learning, sleepiness, and mood. Adenotonsillectomy (AT) is the second most common surgical procedure in children. It is now performed more often for suspected SDB than for any other indication. However, recent studies indicate that many if not most children still have SDB after AT, and many still have learning or behavioral problems associated with SDB. The goals of this study are: (1) to assess the extent that behavior, cognition, and sleepiness in children can improve with Continuous positive airway pressure (CPAP) treatment after AT, and (2) to identify which patients stand to gain most from post-operative assessment and treatment.
Detailed Description
Obstructive sleep-disordered breathing (SDB) affects at least 2-3% of children and may have substantial adverse impact on behavior and cognition. Adenotonsillectomy (AT), the second most common surgical procedure in children, is now performed more often for suspected SDB than for any other indication. However, recent studies among an increasingly obese population now show something alarming: many if not most children still have SDB after AT, and many still suffer from residual neurobehavioral morbidity. Furthermore, the investigators' ongoing, 12-year, NIH-funded research has shown that standard preoperative polysomnographic measures of SDB do not consistently predict post-AT improvement in behavior and cognition. This may arise in part because many children after AT still have SDB, and because linear relationships between standard SDB measures and neurobehavioral morbidity may not exist. Even at subtle levels, SDB may promote significant neurobehavioral morbidity. Some have suggested that polysomnography may be more important after AT than before AT. However, in practice few children receive polysomnography before AT, and even fewer after AT, when continuous positive airway pressure (CPAP) could still provide definitive relief from SDB. Preliminary data from our group suggest that CPAP after AT is well-tolerated by most children and may provide significant benefit. However, virtually no published evidence exists to address critical clinical questions: which children benefit most from CPAP after AT; what role can clinical symptoms or polysomnography play in that determination; and what neurobehavioral gains are achieved by CPAP after AT? The investigators therefore will undertake a highly practical, clinical study with two main goals: (1) to assess the extent that behavior, cognition, and sleepiness in children can improve with CPAP after AT, and (2) to identify which patients stand to gain most from post-operative assessment and treatment. This research will use reversible SDB-related neurobehavioral morbidity as the criteria by which to judge the utility of clinical symptoms and polysomnography in identification of candidates for CPAP after AT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive, Sleep Apnea Syndromes, Child Behavior Disorders, Attention Deficit Disorder With Hyperactivity, Disorders of Excessive Somnolence
Keywords
polysomnography, child, continuous positive airway pressure, tonsillectomy, neuropsychological tests, cognition, sleepiness, behavior

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CPAP treatment
Arm Type
Experimental
Arm Description
Children randomized to this arm will receive 6 months of CPAP (or BPAP) treatment, beginning at approximately 4 months after AT, in addition to standard of care. For analysis purposes those children who were non-adherent (CPAP use <4 hours per night) vs. adherent (CPAP use at least 4 hours per night) will be analyzed separately.
Arm Title
No CPAP treatment
Arm Type
Other
Arm Description
Children randomized to this comparison arm will not be treated with CPAP or BPAP, but will be followed for approximately 10 months after AT while receiving standard of care.
Intervention Type
Procedure
Intervention Name(s)
CPAP treatment
Other Intervention Name(s)
Continuous positive airway pressure device (CPAP), Bi-level positive airway pressure device (BPAP), Positive Airway Pressure device (PAP)
Intervention Description
6 months of treatment with PAP (CPAP or BPAP)
Intervention Type
Other
Intervention Name(s)
No CPAP treatment
Other Intervention Name(s)
Comparison group, Control group
Intervention Description
Children randomized to the comparison group will receive routine care
Primary Outcome Measure Information:
Title
Change in Behavioral Index After 6 Months of CPAP or No-CPAP
Description
The sum of the T-scores of The Conners' Parent Rating Scales (CPRS-R:L, ADHD index) and the Child Behavior Checklist (CBCL, Attention Deficit/Hyperactivity Problems) are used to construct the primary study outcome measure Behavioral Index. Behavioral index is a T score (adjusted for age and gender) with a range of "<10" to ">90" - where higher scores mean worse behavior and lower scores mean better behavior, so a negative change score represents an improvement in behavior. T-scores with a mean of 50 and SD of 10 are computed.
Time Frame
assessed as change from baseline to 6 months of CPAP therapy or no-CPAP
Secondary Outcome Measure Information:
Title
Change in Cognition as Shown by NIH Toolbox Composite Score
Description
Scores are reported as standardized scores with a mean of 100 and SD of 15. Minimum value 40 and Maximum value 160. Higher scores are better
Time Frame
assessed as change from baseline to 6 months of CPAP therapy or no-CPAP
Title
Change in Sleepiness as Measured by Epworth Sleepiness Scale
Description
Epworth Sleepiness Scale scores range from 0 to 24 where higher scores mean greater sleepiness.
Time Frame
assessed as change from baseline to 6 months of CPAP therapy or no-CPAP
Title
Change in Sleepiness After AT as Measured by Multiple Sleep Latency Test (MSLT)
Description
Multiple Sleep Latency Test (MSLT) is an objective measure of sleepiness determined by measure of brain waves and other physiological signals over a 30 minute period. This is measured for five 30 minute periods across the day and average latency to sleep for each participant across those times were used to calculate the mean sleep latency. The score is measured in how quickly one would fall asleep, measured in minutes, so a negative number of minutes in the change score means that participants fell asleep more quickly than previously.
Time Frame
assessed as change from baseline to 6 months of CPAP therapy or no-CPAP
Title
Change in Quality of Life as Measured by Peds QL
Description
Peds-QL is a quality of life symptom measurement with a score range of 0 to 100. Higher scores are better quality of life
Time Frame
assessed as change from baseline to 6 months of CPAP therapy or no-CPAP
Title
CPAP Adherence as Measured by Number of Participants Who Used the CPAP Consistently.
Description
CPAP adherence data will be downloaded from CPAP machines. It is defined for this study as using the CPAP machine for at least an average of 4 hours per night during the last 60 days of the assignment.
Time Frame
Starting at 4 months after AT and continuing through 10 months after AT
Other Pre-specified Outcome Measures:
Title
Change in Cognition as Measured by Fluid Cognition Scores
Description
Scores are reported as standardized scores with a mean of 100 and SD of 15. Minimum value 40, Maximum value 160. Higher scores are better
Time Frame
assessed as change from baseline to 6 months of CPAP therapy or no-CPAP
Title
Change in Cognition After AT as Shown by Academic Achievement
Description
Academic achievement mean score is a standardized score with a mean of 100 and SD 15. Minimum value 40 and Maximum value 160. Higher scores are better
Time Frame
assessed as change from baseline to 6 months of CPAP therapy or no-CPAP

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children ages 5-12 years old, Scheduled for an adenotonsillectomy for treatment of sleep apnea, Child must provide assent, and Parent or legal guardian must be able to speak and read English, and agree to the study. Exclusion Criteria: No siblings of children already enrolled in the study, Children who expect to have another surgery (in addition to AT) during the period of participation in this study, Neurological, psychiatric, or medical conditions, or social factors that may affect test results, prevent children from returning for required study visits, or interfere with the study treatment, or Certain medications that affect sleepiness or alertness, for example: Stimulants (such as Ritalin, Adderall, or Concerta), Sleep aides (such as Melatonin, Ambien, or Ativan), or Sedating medicines (such as Benadryl, Klonopin, Xanax, or Valerian).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ronald D. Chervin, MD, MS
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan Health System
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

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Continuous Positive Airway Pressure (CPAP) After Adenotonsillectomy in Children

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