Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02703207 · ClinicalTrials.gov registry record · NA

Neurocognitive and Health Impact of Sleep Apnea in Elderly Veterans With Comorbid COPD

A NA study of Obstructive Sleep Apnea and OSA COPD Overlap Syndrome, sponsored by VA Office of Research and Development.

Recruiting
Registry status
NA
Development phase
108
Enrollment target
1
Study location

NCT02703207: Recruiting NA study of Obstructive Sleep Apnea and OSA COPD Overlap Syndrome, sponsored by VA Office of Research and Development.

NCT02703207 is a NA study of Obstructive Sleep Apnea and OSA COPD Overlap Syndrome that is actively recruiting participants, run by VA Office of Research and Development. The registered enrollment target is 108 participants, below the 221-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (51% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02703207, a NA study of Obstructive Sleep Apnea and OSA COPD Overlap Syndrome, is actively recruiting participants, sponsored by VA Office of Research and Development.

RECRUITING
Registry status
NA
Development phase
108 participants
Enrollment target
1
Study location

Study Summary

Cognitive dysfunction in the aging Veteran population is a growing health concern in the Veterans Health System. It is not known whether OSA coexisting with COPD will enhance the risk for cognitive dysfunction. The investigators sought to investigate whether these two highly prevalent diseases, that often co-exist as the 'Overlap Syndrome', combine to enhance cognitive impairment in the elderly Veteran population. Thus, the investigators will study whether elderly patients with Overlap syndrome have increased cognitive deficits compared with OSA or COPD alone. Additionally, treatment of OSA with positive airway pressure (PAP) has been shown to improve neurocognitive function in moderate-to-severe OSA while cognitive decline in COPD may be reversible through treatment with long-term oxygen therapy. The investigators will also study whether treatment with positive airway pressure (PAP) and supplemental oxygen vs PAP alone will improve cognitive function and improve quality of life of elderly Veterans.

Primary Outcome

The neurocognitive test - Trails A test will be administered to evaluate attention and psychomotor function. This score is adjusted for age, race, gender, and years of education. Scored on a Standard scale of 100 +/- 15 for normal ranges, above 115 is above average, below 85 is considered below average.

Interventions

  • DEVICE Positive airway pressure
  • DEVICE NIPPV and /or oxygen

Study Locations (1)

Michigan

  • John D. Dingell VA Medical Center, Detroit, MI - Detroit

Trial Details

FieldValue
Enrollment Target 108 participants
Start Date 2016-08-17
Est. Completion 2026-12-31
Phase NA
VA Office of Research and Development

1,668 total trials

What NCT02703207 shows while recruiting

NCT02703207 is an interventional study that assigns participants to a tested intervention. The registered 108 participants enrollment target is mid-sized for trials with a published cap, below the 221-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (51% lower).

The record links to 2 conditions, with Obstructive Sleep Apnea appearing as the primary indexed condition, and to 2 interventions - of which Positive airway pressure is the first listed.

NCT02703207 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT02703207 about?

NCT02703207 is a clinical study titled "Neurocognitive and Health Impact of Sleep Apnea in Elderly Veterans With Comorbid COPD". Cognitive dysfunction in the aging Veteran population is a growing health concern in the Veterans Health System. It is not known whether OSA coexisting with COPD will enhance the risk for cognitive dysfunction. The investigators sought to investigate whether these two highly prevalent diseases, that...

What is the current status of trial NCT02703207?

This trial is currently recruiting. It is a NA study. The enrollment target is 108 participants. The study started on 2016-08-17. Estimated completion is 2026-12-31.

What conditions does trial NCT02703207 study?

This clinical trial studies the following conditions: Obstructive Sleep Apnea, OSA COPD Overlap Syndrome.

What interventions are being tested in trial NCT02703207?

The interventions under investigation include: Positive airway pressure (DEVICE), NIPPV and /or oxygen (DEVICE).

Who is sponsoring clinical trial NCT02703207?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02703207 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Obstructive Sleep Apnea

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 NCT02703207's enrollment target sits among peer trials

108 67th of 155 higher than 89 of 155 other Obstructive Sleep Apnea trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Obstructive Sleep Apnea 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.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02744677 · 108 participants · NA

    COMPASSION S3 - Evaluation of the SAPIEN 3 Transcatheter Heart Valve in Patients With Pulmonary Valve Dysfunction

  • NCT02781883 · 108 participants · Phase 2

    Clinical Trial of BP1001 in Combination With With Venetoclax Plus Decitabine in AML

  • NCT03848663 · 108 participants · NA

    Visual Remapping to Aid Reading With Field Loss

  • NCT04229043 · 108 participants · NA

    Gastric Emptying of Water and Sports Drink in Labor

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02703207, the US trial registry maintained by the National Library of Medicine. NCT02703207 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.