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NCT07301710 · ClinicalTrials.gov registry record · Phase 1
Low-Tech Treatments for Obstructive Sleep Apnea
A Phase 1 study of Obstructive Sleep Apnea (OSA) and Traumatic Brain Injury (TBI), sponsored by Uniformed Services University of the Health Sciences.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT07301710: Recruiting Phase 1 study of Obstructive Sleep Apnea (OSA) and Traumatic Brain Injury (TBI), sponsored by Uniformed Services University of the Health Sciences.
NCT07301710 is a Phase 1 study of Obstructive Sleep Apnea (OSA) and Traumatic Brain Injury (TBI) that is actively recruiting participants, run by Uniformed Services University of the Health Sciences. The registered enrollment target is 60 participants, below the 587-participant average among 12 other Obstructive Sleep Apnea (OSA) trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07301710, a Phase 1 study of Obstructive Sleep Apnea (OSA) and Traumatic Brain Injury (TBI), is actively recruiting participants, sponsored by Uniformed Services University of the Health Sciences.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
The overall purpose of this study is to compare changes in sleep outcomes in people with obstructive sleep apnea (OSA) depending on their participation in one of two behavioral interventions; both involve drinking water and breathing. A second purpose is to compare outcomes between people who have sustained a traumatic brain injury (TBI) and those with no history of TBI. The main questions it aims to answer are whether sleep quality improves after 3-months of high-resistance versus low-resistance exercises, and whether people have different outcomes depending on their history of TBI.
Primary Outcome
AHI is the number of apneic and hypopneic episodes per hour of sleep. The scores start at zero, meaning no events are taking place. A mild score falls in the range of 5-15; moderate 15-30, and a severe diagnosis is 30 or more events per hour. Pre-intervention AHI is obtained from standard-of-care in-clinic sleep study. Post-intervention AHI is obtained from an in-clinic sleep study conducted as part of this research.
Conditions Studied
Interventions
- BEHAVIORAL High-Resistance Breathing and Drinking Exercises
- BEHAVIORAL Low-Resistance Breathing and Drinking Exercises
Study Locations (1)
Maryland
- Walter Reed National Military Medical Center - Bethesda
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2026-01-29 |
| Est. Completion | 2027-12 |
| Phase | Phase 1 |
What NCT07301710 shows while recruiting
NCT07301710 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 587-participant average among 12 other Obstructive Sleep Apnea (OSA) trials with a reported enrollment target (90% lower).
The record links to 2 conditions, with Obstructive Sleep Apnea (OSA) appearing as the primary indexed condition, and to 2 interventions - of which High-Resistance Breathing and Drinking Exercises is the first listed.
NCT07301710 reports a single indexed study location in Maryland.
Frequently Asked Questions
What is clinical trial NCT07301710 about?
NCT07301710 is a clinical study titled "Low-Tech Treatments for Obstructive Sleep Apnea". The overall purpose of this study is to compare changes in sleep outcomes in people with obstructive sleep apnea (OSA) depending on their participation in one of two behavioral interventions; both involve drinking water and breathing. A second purpose is to compare outcomes between people who have s...
What is the current status of trial NCT07301710?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2026-01-29. Estimated completion is 2027-12.
What conditions does trial NCT07301710 study?
This clinical trial studies the following conditions: Obstructive Sleep Apnea (OSA), Traumatic Brain Injury (TBI).
What interventions are being tested in trial NCT07301710?
The interventions under investigation include: High-Resistance Breathing and Drinking Exercises (BEHAVIORAL), Low-Resistance Breathing and Drinking Exercises (BEHAVIORAL).
Who is sponsoring clinical trial NCT07301710?
This trial is sponsored by Uniformed Services University of the Health Sciences, which has 27 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07301710 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Obstructive Sleep Apnea (OSA)
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT07301710's enrollment target sits among peer trials
60 5th of 12 higher than 7 of 12 other Obstructive Sleep Apnea (OSA) trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Obstructive Sleep Apnea (OSA) trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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