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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02114424
Other study ID # H-3-2014-039
Secondary ID
Status Not yet recruiting
Phase Phase 2/Phase 3
First received April 10, 2014
Last updated April 13, 2014
Start date May 2014
Est. completion date February 2016

Study information

Verified date April 2014
Source Glostrup University Hospital, Copenhagen
Contact Philip Toennesen, M.D., Ph.D.
Phone (45)51264850
Email philip.toennesen.01@regionh.dk
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research EthicsDenmark: Danish Dataprotection Agency
Study type Interventional

Clinical Trial Summary

POSAS can be treated with CPAP however there is now evidence from a few studies that Night Balance is effective in POSAS. Night Balance seems to be better accepted than CPAP so we would like to examine if we could find similar results in routine clinical work and especially we would like to confirm the subjective effects with objective measures i.e. a reduction in AHI in the supine position during sleep.


Description:

Primary aim: Efficacy and adherence of Night Balance in POSAS versus no therapy after 2 months (Sleep supine).

Secondary aim: Efficacy and adherence of Night Balance in POSAS after a 6 months period (Sleep supine and compliance and AHI).

Nigh Balance is a vibrator and a belt that vibrate when laying supine so that after a few days you will not sleep supine.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date February 2016
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- AHI supine = AHI non-supine x 2,

- AHI supine = 10

- AHI non-supine <10

- 10 -90 % sleep time in supine position

- Daytime tiredness and/or disturbed sleep and/or snoring

Exclusion Criteria:

- Not able or willing to cooperate

- Age <18 years

- Central Sleep Apnea

- Night or shifting work

- Severe chronic heart failure or severe COPD

- A medical history of known causes of tiredness by day or severe sleep disruption (insomnia, PLMS, Narcolepsy)

- Seizure disorder

- A known medical history of mental retardation, memory disorders or psychiatric disorders

- The inability to provide informed consent

- Pacemaker

- Pain in joints or shoulder

- Other reasons unable to sleep in lateral positions.

- Pregnant females or females that plan pregnancy in study period (problems sleeping supine)

- Breastfeeding females in study period (other reasons for disturbed sleep)

- Plan weight reduction in study period

- Plan to quit smoking in study period

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Device:
Positional vibrator belt
Belt with vibarator to avoid sleep supine

Locations

Country Name City State
Denmark Glostrup University Hospital Glostrup

Sponsors (1)

Lead Sponsor Collaborator
Glostrup University Hospital, Copenhagen

Country where clinical trial is conducted

Denmark, 

References & Publications (1)

23. van der Star A, Mekking S, van Riet M. The technical validation of the Sleep Position Trainer. Nightbalance Research and Development [Internet]. 2012 Oct [cited 2013 Dec 6]:1-12. Available from http://www.nightbalance.com/research.

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy and adherence of Night Balance in POSAS versus no therapy after 2 months (Sleep supine and AHI). AFter 2 months assessment will be done by sleep questionnaires and CRM After 2 months No
Secondary Efficacy and adherence of Night Balance in POSAS versus no therapy after 2 months (Sleep supine). ALl wil ahve a new CRM after 6 months with Night Balance and sleep questionnaires 6 months after entry Yes