Primary hypothesis: Position therapy reduces sleep time in supine posture using the Sleep Position Trainer (SPT) in equal amount as the position band (PB) in patients with mild and moderate positional OSAS. Secondary hypothesis: The Sleep…
ID
Bron
Verkorte titel
Aandoening
Positional Obstructive Sleep Apnea Syndrome, OSAS
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Sleeping time in supine posture as percentage of total sleep time (%STS) and compliance.
Achtergrond van het onderzoek
Rationale:
This study tries to answer the call for the search of a comfortable and ergonomic positional therapy, which increases compliance for positional therapy in posture dependent OSAS patients.
Objective:
To assess equivalence in reducing sleep time in supine posture between positional therapy using the position training device and the sleep position band in patients with mild and moderate positional OSAS.
Design:
This study will be conducted according to an open randomized controlled trial design at Medisch Spectrum Twente, Enschede.
Population:
The subjects for the study will be recruited from the department of pulmonary medicine at Medisch Spectrum Twente in Enschede and Oldenzaal, the Netherlands. Subjects will be males and females with diagnosis of symptomatic mild or moderate OSAS (5 < AHI < 30) and the diagnosis positional OSAS (2*AHInonsupine ≤ AHIsupine & AHInonsupine < 5).
Intervention:
Subjects will sleep every night with the position training device during a 1 month period. The small device is placed in an elastic band stretched around the subject's lower chest. During sleep the device registers the sleep position of the subject and it will vibrate when the subject lays in supine posture. The positional therapy that is used as control consists of the subject getting a sleep position band. Whenever a patient rolls into supine posture during sleep, he feels the pressure of the ball and is likely to change his posture.
Doel van het onderzoek
Primary hypothesis: Position therapy reduces sleep time in supine posture using the Sleep Position Trainer (SPT) in equal amount as the position band (PB) in patients with mild and moderate positional OSAS.
Secondary hypothesis: The Sleep Position Trainer (SPT) increases patient's compliance compared to the position band (PB).
Onderzoeksopzet
Subjects will sleep with the device during a 1 month period. Measurements will take place before and right after the intervention.
Onderzoeksproduct en/of interventie
Subjects will sleep every night with the position training device during a 1 month period. The small device is placed in an elastic band stretched around the subject's lower chest. During sleep the device registers the sleep position of the subject and it will vibrate when the subject lays in supine posture.
The positional therapy that is used as control consists of the subject getting a sleep position band. Whenever a patient rolls into supine posture during sleep, he feels the pressure of the obstruction and is likely to change his posture.
Publiek
P.O. Box 50000
M.M.M. Eijsvogel
Enschede 7500 KA
The Netherlands
+31 (0)53 4872628
Wetenschappelijk
P.O. Box 50000
M.M.M. Eijsvogel
Enschede 7500 KA
The Netherlands
+31 (0)53 4872628
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. 18 years or older;
2. Ability to understand, read and write Dutch;
3. Ability to follow up;
4. Diagnosis of symptomatic mild or moderate OSAS (5 < AHI < 30);
5. Diagnosis positional OSAS (2*AHInonsupine ≤ AHIsupine);
6. AHInonsupine < 5.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Central sleep apnea syndrome / Cheyne-Stokes respiration;
2. Signs of severe nasal obstruction;
3. Major facial or pharyngeal anatomic abnormalities likely to require surgery;
4. Night or rotating shift work;
5. Severe chronic heart failure;
6. Known history of a known cause of daytime sleepiness and severe sleep disruption (e.g. insomnia, PLMS, narcolepsy);
7. Seizure disorder;
8. Known medical history of mental retardation, memory disorders or psychiatric disorders;
9. The inability to provide informed consent.
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In overige registers
Register | ID |
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NTR-new | NL2604 |
NTR-old | NTR2732 |
CCMO | NL34934.044.10 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |
OMON | NL-OMON36753 |