Respiratory-Swallow Coordination in Cardiothoracic Surgical Patients

NCT ID: NCT05173207

Last Updated: 2022-07-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

8 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-03

Study Completion Date

2022-07-27

Brief Summary

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Dysphagia (swallowing impairment) is a common complication of cardiothoracic surgery (CS). Although alterations in respiratory-swallow coordination is a known underlying pathophysiologic mechanism of dysphagia in multiple patient populations, no group has examined respiratory-swallow physiology in CS patients. The proposed study will examine respiratory-swallow physiology in CS patients and determine its association with unsafe swallowing and inferior health-related outcomes.

Detailed Description

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The proposed study will examine respiratory-swallow physiology in cardiothoracic surgical patients and determine its association with unsafe swallowing and inferior health-related outcomes. Participation will involve a single postoperative research exam of approximately 60-90 minute duration. Participants will be seated upright and positioned for simultaneous instrumental imaging of swallow physiology, nasal airflow monitoring, and respiratory inductance plethysmography testing.

Conditions

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Thoracic Diseases Cardiovascular Diseases

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cardiothoracic surgical patients

Subjects will undergo one simultaneous instrumental examination of swallowing and concurrent monitoring of metrics of respiratory-swallow physiology. Research exam will be performed at bedside within Cardiac \& Thoracic Intensive Care Units during their early postoperative recovery.

Videofluoroscopic swallow exam with concurrent monitoring of respiratory-swallow coordination

Intervention Type DIAGNOSTIC_TEST

Participants will undergo simultaneous videofluoroscopy, nasal airflow and respiratory inductance plethysmography testing.

Interventions

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Videofluoroscopic swallow exam with concurrent monitoring of respiratory-swallow coordination

Participants will undergo simultaneous videofluoroscopy, nasal airflow and respiratory inductance plethysmography testing.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Adults over 18 years of age who have undergone cardiothoracic surgery at UF Health
* No allergies to barium
* Not pregnant
* Willing to participate in study

Exclusion Criteria

* Individuals 18 years of age or younger
* Allergies to barium
* Pregnant
* Not willing to participate in study
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Florida

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Emily K Plowman, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Locations

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University of Florida

Gainesville, Florida, United States

Site Status

Countries

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United States

Other Identifiers

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IRB202102635

Identifier Type: -

Identifier Source: org_study_id

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