Telehealth for Sleep Apnea: Effectiveness, Implementation, and Cost in the Military Health System
Recruiting
N/A
Interventional Study
Obstructive Sleep Apnea (OSA)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 64
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 160 (estimated)
- Sponsor
- Uniformed Services University of the Health Sciences · Federal
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About This Trial
The long-term goal of this research is to improve military health and operational readiness among military service members with sleep disorders. The overall objective of the current study is to 1) determine the clinical effectiveness (non-inferiority) and cost-effectiveness of OSA telehealth care, including a human sleep navigator (vs private sector care), and 2) to perform a formative evaluation …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Age 18-64 years
2. ADFM or DEERS beneficiary
3. Enrolled in any TRICARE (Prime, Standard, or Extra)
4. Deferred to private sector care (i.e., local TRICARE network) for OSA care
5. Newly diagnosed with OSA (AHI\>5)
6. Access to smartphone, desktop, laptop, or tablet computer
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Contacts