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Clinical Trials/NCT02509247
NCT02509247
Completed
Not Applicable

Telemonitoring in CPAP Treatment

Turku University Hospital1 site in 1 country111 target enrollmentAugust 2012
ConditionsSleep Apnea

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep Apnea
Sponsor
Turku University Hospital
Enrollment
111
Locations
1
Primary Endpoint
Nursing time
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Wireless telemonitoring was used during the habituation phase of continuous positive airway pressure (CPAP) treatment in obstructive sleep apnoea (OSA) patients. Patients were allocated either to the telemonitoring group (n=50) or the usual care group (n=61). Nursing time, patient satisfaction and treatment efficiency and efficacy were compared between the groups at baseline and after one year treatment the CPAP adherence and treatment efficacy were recorded.

Detailed Description

Wireless telemonitoring was used during the habituation phase of continuous positive airway pressure (CPAP) treatment in obstructive sleep apnoea (OSA) patients. Patients were allocated either to the telemonitoring group (n=50) or the usual care group (n=61). Nursing time, patient satisfaction and treatment efficiency and efficacy were compared between the groups at baseline and after one year treatment the CPAP adherence and treatment efficacy were recorded. This study was part of our regular testing and quality assurance procedure when developing and revising clinical treatment protocol of sleep apnoea patients. When planning remarkable changes in treatment protocol we have to test whether it is feasible and cost-effective to change the protocol. The data was retrospectively collected from hospital records and nurses' notes (nursing time). According to instructions of our hospital, the Ethics Committee approval is not required. The approval of the hospital (Head of the Division of Medicine) for testing the wireless telemonitoring system of CPAP treatment was applied and received (Protocol Record T200/2013, diary number TO5/049/13). Written informed consent was obtained from those patients allocated to the telemonitoring group.

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
March 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Consecutive adult patients commencing CPAP therapy for OSA

Exclusion Criteria

  • Patient not able to co-operate

Outcomes

Primary Outcomes

Nursing time

Time Frame: 3 months

Nursing time includes patient's visit at nurse office, phone calls, check-ups of telemonitoring data and completing patient records

Secondary Outcomes

  • CPAP adherence measured with in-built clock counter(1 year)

Study Sites (1)

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