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Study to Predict the Need for Humidification Use and Comparison of the Effect of ThermoSmart™ and no Humidification on Adherence

Primary Purpose

Sleep Apnea, Obstructive

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
ICON Auto CPAP™ with Thermosmart heated tube
ICON Auto CPAP™ without Thermosmart heated tube
Sponsored by
Fisher and Paykel Healthcare
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Apnea, Obstructive focused on measuring Obstructive Sleep Apnea, Humidification, Continuous Positive Airway Pressure, ICON, ThermoSmart

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed with OSA
  • Naïve to CPAP therapy, i.e have not been prescribed, or used CPAP in the last 5 years
  • Prescribed a nasal mask (as patients will be prescribed their mask following recruitment into the study, any participants who are prescribed a full face mask will be withdrawn)

Exclusion Criteria:

  • Severe heart disease
  • Co-existing lung disease
  • Co-existing sleep disorders
  • Pregnant

Sites / Locations

  • Helios - Klinik Ambrock

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

APAP with humidification

APAP without humidification

Arm Description

ICON Auto CPAP™ with Thermosmart heated tube

ICON Auto CPAP™ without Thermosmart heated tube

Outcomes

Primary Outcome Measures

Therapy Adherence With Treatment Per Night Averaged Over Total Time Period Measured Via Internal Software on the Device and Reported on Using InfoSmart™ Software With and Without Heated Humidification.

Secondary Outcome Measures

Epworth Sleepiness Score (ESS)
The ESS is a measure of daytime sleepiness and has a total of 24 points. A range from 0-9 is considered normal. A score of more than 9 is considered to have abnormal daytime sleepiness
Functional Outcome of Sleep Questionnaire (FOSQ)
FOSQ is a measure of the impact of the disorder on multiple activities with everyday living and how the treatment can improve these activities. There are 30 questions and for each questions you have to pick from a subscale from 0-4; 0 = "I don't do this activity for other reasons", 1="Yes extremely", 2="Yes moderately", 3= "Yes a little", 4 = "No". Scores of each subscale will be summed up and scaled to a maximum achievable value of 20. The sum score was calculated. The value range is 0-100. A higher score means that the treatment has positively improved everyday activities.
Nasopharyngeal Complaints
Nasopharyngeal complaints (NPC) were assessed by a questionnaire. Subjects were asked to evaluate their condition on a scale from 0 ("no complaints") to 5 ("very strong"). The following questions were asked within the questionnaire: Did you observe nasal congestion, nasal dryness, runny nose, dry mouth, and dry throat (0-5 each) during the last week. The maximal achievable sum score was 25.

Full Information

First Posted
January 18, 2012
Last Updated
June 21, 2015
Sponsor
Fisher and Paykel Healthcare
Collaborators
Helios Klinik Ambrock
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1. Study Identification

Unique Protocol Identification Number
NCT01517750
Brief Title
Study to Predict the Need for Humidification Use and Comparison of the Effect of ThermoSmart™ and no Humidification on Adherence
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fisher and Paykel Healthcare
Collaborators
Helios Klinik Ambrock

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Despite the effectiveness of continuous positive airway pressure (CPAP) in abolishing upper airway obstruction, acceptance of and adherence with therapy has been sub-optimal. One of the only technological advancements shown to increase adherence is heated humidification, now considered part of conventional CPAP therapy in some countries. ThermoSmart™ is a unique technology developed by Fisher & Paykel Healthcare which utilises a heated breathing tube to deliver optimal humidity in all environments. ThermoSmart has been shown to be superior to conventional humidification in reducing side effects, condensation and titrated pressure as well as increasing total sleep time. However, improved humidity delivery has not lead to significantly increased adherence in unselected obstructive sleep apnea (OSA) patients. A total of 80 patients diagnosed with OSA but naive to CPAP use will be randomized into a single blind, randomized, parallel-arm trial to determine whether the the use of heated humidification will impact therapy adherence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive
Keywords
Obstructive Sleep Apnea, Humidification, Continuous Positive Airway Pressure, ICON, ThermoSmart

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
APAP with humidification
Arm Type
Experimental
Arm Description
ICON Auto CPAP™ with Thermosmart heated tube
Arm Title
APAP without humidification
Arm Type
Active Comparator
Arm Description
ICON Auto CPAP™ without Thermosmart heated tube
Intervention Type
Device
Intervention Name(s)
ICON Auto CPAP™ with Thermosmart heated tube
Intervention Description
ICON Auto CPAP™ with heated humidification and the use of a heated tube
Intervention Type
Device
Intervention Name(s)
ICON Auto CPAP™ without Thermosmart heated tube
Intervention Description
ICON Auto CPAP™ without heated humidification or the use of a heated tube.
Primary Outcome Measure Information:
Title
Therapy Adherence With Treatment Per Night Averaged Over Total Time Period Measured Via Internal Software on the Device and Reported on Using InfoSmart™ Software With and Without Heated Humidification.
Time Frame
6 weeks after patient randomization
Secondary Outcome Measure Information:
Title
Epworth Sleepiness Score (ESS)
Description
The ESS is a measure of daytime sleepiness and has a total of 24 points. A range from 0-9 is considered normal. A score of more than 9 is considered to have abnormal daytime sleepiness
Time Frame
6 weeks after patient randomization
Title
Functional Outcome of Sleep Questionnaire (FOSQ)
Description
FOSQ is a measure of the impact of the disorder on multiple activities with everyday living and how the treatment can improve these activities. There are 30 questions and for each questions you have to pick from a subscale from 0-4; 0 = "I don't do this activity for other reasons", 1="Yes extremely", 2="Yes moderately", 3= "Yes a little", 4 = "No". Scores of each subscale will be summed up and scaled to a maximum achievable value of 20. The sum score was calculated. The value range is 0-100. A higher score means that the treatment has positively improved everyday activities.
Time Frame
6 weeks after patient randomization
Title
Nasopharyngeal Complaints
Description
Nasopharyngeal complaints (NPC) were assessed by a questionnaire. Subjects were asked to evaluate their condition on a scale from 0 ("no complaints") to 5 ("very strong"). The following questions were asked within the questionnaire: Did you observe nasal congestion, nasal dryness, runny nose, dry mouth, and dry throat (0-5 each) during the last week. The maximal achievable sum score was 25.
Time Frame
6 weeks after patient randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with OSA Naïve to CPAP therapy, i.e have not been prescribed, or used CPAP in the last 5 years Prescribed a nasal mask (as patients will be prescribed their mask following recruitment into the study, any participants who are prescribed a full face mask will be withdrawn) Exclusion Criteria: Severe heart disease Co-existing lung disease Co-existing sleep disorders Pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Georg Nilius, Dr.
Organizational Affiliation
Helios Klinik Ambrock
Official's Role
Principal Investigator
Facility Information:
Facility Name
Helios - Klinik Ambrock
City
Hagen
State/Province
Weg
ZIP/Postal Code
60
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
25957615
Citation
Nilius G, Franke KJ, Domanski U, Schroeder M, Ruhle KH. Effect of APAP and heated humidification with a heated breathing tube on adherence, quality of life, and nasopharyngeal complaints. Sleep Breath. 2016 Mar;20(1):43-9. doi: 10.1007/s11325-015-1182-2. Epub 2015 May 10.
Results Reference
derived
Links:
URL
http://www.fphcare.co.nz/
Description
Sponsor Site

Learn more about this trial

Study to Predict the Need for Humidification Use and Comparison of the Effect of ThermoSmart™ and no Humidification on Adherence

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