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Economic Evaluation of Treatment Modalities for Position Dependent Obstructive Sleep Apnea

Primary Purpose

Positional Obstructive Sleep Apnea

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Sleep position trainer
Mandibular advancement device
Continuous positive airway pressure
Sponsored by
Onze Lieve Vrouwe Gasthuis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Positional Obstructive Sleep Apnea focused on measuring Positional therapy, MAD, Oral appliance, Sleep position trainer, POSA

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years and older
  • Ability to speak, read and write Dutch
  • Ability to follow up
  • Diagnosis with symptomatic moderate OSA (15 < AHI < 30)
  • Diagnosis of 10 to 90% supine position during the night
  • AHI supine is 2 > as high as AHI non-supine
  • Own a Windows PC and ability to install SPT connection software and upload research data
  • Expected to maintain current lifestyle (sports, medicine, diet etc.)

Exclusion Criteria:

  • Many dental problems; insufficient teeth for wearing MRA
  • Medication used/ related to sleeping disorders
  • Central Sleep Apnea Syndrome
  • Night or shifting work
  • Severe chronic heart failure
  • Medical history of known causes of tiredness by day or severe sleep disruption (insomnia, PLMS, Narcolepsy)
  • Seizure disorder
  • Known medical history of mental retardation, memory disorders or psychiatric disorders
  • Shoulder, neck and back complaints
  • Reversible morphological upper airway abnormalities (e.g. enlarged tonsils)
  • Inability to provide informed consent
  • Simultaneous use of other treatment modalities to treat OSA
  • Previous treatment for OSA with MRA, CPAP or SPT
  • Pregnancy

Sites / Locations

  • Antwerp University Hospital (UZA)Recruiting
  • OLVG WestRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Combination therapy

CPAPContinuous positive airway pressure

Arm Description

Sleep Position Trainer + Mandibular Advancement device combination The SPT is a sensor that measures the sleeping position, and gives the user feedback about wrong positions with a soft vibration. A user is then able to react to the signal and turn into a non-supine position. To stimulate compliance, information is provided about nightly behaviour, implicating a learning pattern by viewing the data on a home computer. MRA or oral appliances (OA) works by advancing the mandible and its attached soft tissue structures forward they aim to increase upper airway size.

Continuous positive airway pressure (CPAP) functions as a pneumatic splint to maintain upper airway patency. Possible side effect can be related to the interface, pressure and negative social factors.

Outcomes

Primary Outcome Measures

Apnea-hypopnea index (AHI)

Secondary Outcome Measures

Outcome of Quality of Life questionnaires
EQ-5D
Outcome of Quality of Life questionnaires
Epworth Sleeping Scale (ESS)
Outcome of Quality of Life questionnaires
Functional Outcome Sleep Questionnaire (FOSQ)
(Societal) costs of treatment
iMTA Productivity Cost Questionnaire (iPCQ)
(Societal) costs of treatment
iMTA Medical Consumption Questionnaire (iMCQ)
Therapy compliance
Measurement of actual wearing time (in hours) per night
Cardiovascular parameters
Systolic and diastolic blood pressure
Cardiovascular parameters
Pulse rate

Full Information

First Posted
September 14, 2015
Last Updated
April 10, 2018
Sponsor
Onze Lieve Vrouwe Gasthuis
Collaborators
University Hospital, Antwerp
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1. Study Identification

Unique Protocol Identification Number
NCT02553902
Brief Title
Economic Evaluation of Treatment Modalities for Position Dependent Obstructive Sleep Apnea
Official Title
Economic Evaluation of Treatment Modalities for Position Dependent Obstructive Sleep Apnea Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (Actual)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Onze Lieve Vrouwe Gasthuis
Collaborators
University Hospital, Antwerp

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
OBJECTIVES: To evaluate the effect and cost-utility of a combination therapy of SPT+MAD compared with continuous positive airway pressure (CPAP) in patients with moderate positional obstructive sleep apnea (POSA). HYPOTHESIS: The SPT+MAD combination is more cost-effective and effective, in means of reduction of the apnea-hypopnea index (AHI), quality of life and compliance, compared with CPAP. STUDY DESIGN: A multicenter randomized clinical trial (RCT) will be performed with a follow-up of 12 months per patient. Patients will be randomized for CPAP or the combination SPT and MRA. All outcomes will be measured at baseline, month 3, 6 and 12. STUDY POPULATION: Patients diagnosed with moderate POSA according to polysomnography (PSG) results. INTERVENTION / STANDARD INTERVENTION TO BE COMPARED TO: The SPT trains POSA patients to sleep in non-supine positions, CPAP uses positive airway pressure to open the airway; MRA is an intra-oral prosthesis, which holds the mandible in a protrusive position, all to prevent effectively apneic events. OUTCOME MEASURES: AHI, compliance, quality-adjusted life year (QALY), direct and indirect costs, cardiovascular parameters, incremental cost-effectiveness ratio (ICER) SAMPLE SIZE / DATA ANALYSIS: 100 subjects in each treatment group, total of 200 patients. COST-EFFECTIVENESS ANALYSIS / BUDGET IMPACT ANALYSIS: The SPT is expected to improve the cost-effectiveness of overall treatment of POSA patients, and will save annually approximately 35-150 million euros.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Positional Obstructive Sleep Apnea
Keywords
Positional therapy, MAD, Oral appliance, Sleep position trainer, POSA

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Combination therapy
Arm Type
Active Comparator
Arm Description
Sleep Position Trainer + Mandibular Advancement device combination The SPT is a sensor that measures the sleeping position, and gives the user feedback about wrong positions with a soft vibration. A user is then able to react to the signal and turn into a non-supine position. To stimulate compliance, information is provided about nightly behaviour, implicating a learning pattern by viewing the data on a home computer. MRA or oral appliances (OA) works by advancing the mandible and its attached soft tissue structures forward they aim to increase upper airway size.
Arm Title
CPAPContinuous positive airway pressure
Arm Type
Active Comparator
Arm Description
Continuous positive airway pressure (CPAP) functions as a pneumatic splint to maintain upper airway patency. Possible side effect can be related to the interface, pressure and negative social factors.
Intervention Type
Device
Intervention Name(s)
Sleep position trainer
Intervention Type
Device
Intervention Name(s)
Mandibular advancement device
Other Intervention Name(s)
MRA, MAD
Intervention Type
Device
Intervention Name(s)
Continuous positive airway pressure
Primary Outcome Measure Information:
Title
Apnea-hypopnea index (AHI)
Time Frame
change from baseline, after 3, 6 and 12 months
Secondary Outcome Measure Information:
Title
Outcome of Quality of Life questionnaires
Description
EQ-5D
Time Frame
change from baseline, after 3, 6 and 12 months
Title
Outcome of Quality of Life questionnaires
Description
Epworth Sleeping Scale (ESS)
Time Frame
change from baseline, after 3, 6 and 12 months
Title
Outcome of Quality of Life questionnaires
Description
Functional Outcome Sleep Questionnaire (FOSQ)
Time Frame
change from baseline, after 3, 6 and 12 months
Title
(Societal) costs of treatment
Description
iMTA Productivity Cost Questionnaire (iPCQ)
Time Frame
change from baseline, after 3, 6 and 12 months
Title
(Societal) costs of treatment
Description
iMTA Medical Consumption Questionnaire (iMCQ)
Time Frame
change from baseline, after 3, 6 and 12 months
Title
Therapy compliance
Description
Measurement of actual wearing time (in hours) per night
Time Frame
change from baseline, after 3, 6 and 12 months
Title
Cardiovascular parameters
Description
Systolic and diastolic blood pressure
Time Frame
change from baseline, after 3, 6 and 12 months
Title
Cardiovascular parameters
Description
Pulse rate
Time Frame
change from baseline, after 3, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years and older Ability to speak, read and write Dutch Ability to follow up Diagnosis with symptomatic moderate OSA (15 < AHI < 30) Diagnosis of 10 to 90% supine position during the night AHI supine is 2 > as high as AHI non-supine Own a Windows PC and ability to install SPT connection software and upload research data Expected to maintain current lifestyle (sports, medicine, diet etc.) Exclusion Criteria: Many dental problems; insufficient teeth for wearing MRA Medication used/ related to sleeping disorders Central Sleep Apnea Syndrome Night or shifting work Severe chronic heart failure Medical history of known causes of tiredness by day or severe sleep disruption (insomnia, PLMS, Narcolepsy) Seizure disorder Known medical history of mental retardation, memory disorders or psychiatric disorders Shoulder, neck and back complaints Reversible morphological upper airway abnormalities (e.g. enlarged tonsils) Inability to provide informed consent Simultaneous use of other treatment modalities to treat OSA Previous treatment for OSA with MRA, CPAP or SPT Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Patty Vonk, MD
Email
researchkno@olvg.nl
First Name & Middle Initial & Last Name or Official Title & Degree
N de Vries, Professor
Email
n.vries@slaz.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
O.M. Vanderveken, Professor
Organizational Affiliation
University Hospital, Antwerp
Official's Role
Principal Investigator
Facility Information:
Facility Name
Antwerp University Hospital (UZA)
City
Antwerp
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
O.M. Vanderveken, Professor
Facility Name
OLVG West
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
N. de Vries, Professor
Email
n.vries@olvg.nl
First Name & Middle Initial & Last Name & Degree
Patty Vonk, MD
Email
researchkno@olvg.nl

12. IPD Sharing Statement

Plan to Share IPD
No

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Economic Evaluation of Treatment Modalities for Position Dependent Obstructive Sleep Apnea

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