search
Back to results

Effect of the Use of Protective Masks on the Ability to Perform Daily Activities in Patients With Heart Failure or Obstructive Pulmonary Disease

Primary Purpose

Heart Failure, COPD

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Respiratory protective mask
Sponsored by
Centro Cardiologico Monzino
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Heart Failure

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Healthy subjects: Age: 18-80 years Not taking cardiovascular medications No history of cardiovascular disease Normal physical examination Normal ECG Inclusion criteria for subjects with HF: Age: 18-80 years New York Heart Association Class (NYHA) II to III in stable clinical condition Left ventricular ejection fraction (LVEF) <40% Ability to perform a maximal CPET Patients with COPD: Age: 18-80 years Diagnosis of COPD stage GOLD II-III in stable clinical condition Absent concomitant heart disease Ability to perform a maximal CPET Exclusion Criteria: Healthy subjects: Presence of concomitant diseases Patients: Oxygen therapy Inability or contraindication to perform a maximal CPET

Sites / Locations

  • Centro Cardiologico Monzino, IrccsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Wearing mask

Not wearing mask

Arm Description

Subjects will perform a cardiopulmonary exercise test (CPET) and a series of standardized daily activities while wearing a protective mask

Subjects will perform a cardiopulmonary exercise test (CPET) and a series of standardized daily activities in basal conditions

Outcomes

Primary Outcome Measures

Evaluation of differences in VO2 expressed in mL/min/kg
Differences in oxygen consumption (VO2) in different daily activities under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Evaluation of differences in ventilation expressed as L/min
Differences in ventilation (VE) in different daily activities under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.

Secondary Outcome Measures

Evaluation of differences in peripheral saturation (%)
Differences in peripheral saturation under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..
Evaluation of differences in VE/VCO2 (slope during the exercise)
Differences in ventilation/carbon dioxide(VE/VCO2)slope under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Evaluation of differences in heart rate (beats/min)
Differences in heart rate (HR) under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Evaluation of differences in dyspnea (Borg scale)
Differences in dyspnea grade evaluated by Borg scale under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Evaluation of differences in cardiorespiratory parameters during sleep: nocturnal apneas (number of events)
Differences in nocturnal apneas under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..
Evaluation of differences in cardiorespiratory parameters during sleep: nocturnal hypopnea (number of events)
Differences in nocturnal hypopneas events under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..
Evaluation of differences in nocturnal desaturation (%)
Differences in nocturnal desaturation under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..

Full Information

First Posted
February 16, 2023
Last Updated
February 28, 2023
Sponsor
Centro Cardiologico Monzino
search

1. Study Identification

Unique Protocol Identification Number
NCT05762406
Brief Title
Effect of the Use of Protective Masks on the Ability to Perform Daily Activities in Patients With Heart Failure or Obstructive Pulmonary Disease
Official Title
Effect of the Use of Protective Masks on the Ability to Perform Daily Activities in Patients With Heart Failure or Obstructive Pulmonary Disease
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 16, 2021 (Actual)
Primary Completion Date
April 30, 2024 (Anticipated)
Study Completion Date
April 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centro Cardiologico Monzino

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Scientific Rationale: In late 2019 and early 2020, researchers at the Wuhan Institute of Virology identified a potential new etiologic agent, called new coronavirus 2019 (nCoV-2019). Subsequently, the epidemic unleashed by this virus involved the whole world and radically changed the habits of the entire global population. Since that time, in fact, the need to contain the spread of infection through specific social distancing procedures and through the use of personal protective equipment has become compelling. The main tool was the requirement for all citizens to wear masks for airway protection. This measure has thus become in daily use for the majority of the population. Therefore, it has become increasingly important to evaluate the impact of mask wearing on activities of daily living (ADls), both in healthy subjects, for which several evidences have already been brought, and in patients with different diseases, for which data are still insufficient to fully describe the effects. Oxygen consumption and dyspnea during simple activities of daily living (ADLs) have already been studied in patients with heart failure (HF) and chronic obstructive pulmonary disease (COPD), and there is evidence that these subjects compared with healthy subjects perform ADLs at a higher percentage of their peak VO2 with more dyspnea. However, there are still no studies highlighting, however, the consequences of performing such activities while wearing a protective filtering facepiece particles class 2 (FFP2) mask, to date considered the most suitable to preserve the most fragile subjects from infection. In this study, therefore, the investigators aim to asess the effects of these devices on the ability to perform ADLs by evaluating the exchanges of respiratory gases in the body during the performance of normal activities or during sleep in patients with HF or COPD compared with healthy subjects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, COPD

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Wearing mask
Arm Type
Experimental
Arm Description
Subjects will perform a cardiopulmonary exercise test (CPET) and a series of standardized daily activities while wearing a protective mask
Arm Title
Not wearing mask
Arm Type
No Intervention
Arm Description
Subjects will perform a cardiopulmonary exercise test (CPET) and a series of standardized daily activities in basal conditions
Intervention Type
Device
Intervention Name(s)
Respiratory protective mask
Intervention Description
Subjects will perform a cardiopulmonary exercise test (CPET) and a series of standardized daily activities while wearing a protective mask. During the exercises, oxygen consumption, ventilation and other cardiorespiratory parameters will be assessed using a portable device (K5, Cosmed)
Primary Outcome Measure Information:
Title
Evaluation of differences in VO2 expressed in mL/min/kg
Description
Differences in oxygen consumption (VO2) in different daily activities under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Time Frame
2 weeks
Title
Evaluation of differences in ventilation expressed as L/min
Description
Differences in ventilation (VE) in different daily activities under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Evaluation of differences in peripheral saturation (%)
Description
Differences in peripheral saturation under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..
Time Frame
2 weeks
Title
Evaluation of differences in VE/VCO2 (slope during the exercise)
Description
Differences in ventilation/carbon dioxide(VE/VCO2)slope under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Time Frame
2 weeks
Title
Evaluation of differences in heart rate (beats/min)
Description
Differences in heart rate (HR) under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Time Frame
2 weeks
Title
Evaluation of differences in dyspnea (Borg scale)
Description
Differences in dyspnea grade evaluated by Borg scale under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients.
Time Frame
2 weeks
Title
Evaluation of differences in cardiorespiratory parameters during sleep: nocturnal apneas (number of events)
Description
Differences in nocturnal apneas under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..
Time Frame
2 weeks
Title
Evaluation of differences in cardiorespiratory parameters during sleep: nocturnal hypopnea (number of events)
Description
Differences in nocturnal hypopneas events under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..
Time Frame
2 weeks
Title
Evaluation of differences in nocturnal desaturation (%)
Description
Differences in nocturnal desaturation under basal conditions and while wearing the protective mask (FFP2) in healthy subjects, heart failure patients and in COPD patients..
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy subjects: Age: 18-80 years Not taking cardiovascular medications No history of cardiovascular disease Normal physical examination Normal ECG Inclusion criteria for subjects with HF: Age: 18-80 years New York Heart Association Class (NYHA) II to III in stable clinical condition Left ventricular ejection fraction (LVEF) <40% Ability to perform a maximal CPET Patients with COPD: Age: 18-80 years Diagnosis of COPD stage GOLD II-III in stable clinical condition Absent concomitant heart disease Ability to perform a maximal CPET Exclusion Criteria: Healthy subjects: Presence of concomitant diseases Patients: Oxygen therapy Inability or contraindication to perform a maximal CPET
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Piergiuseppe Agostoni, Prof
Phone
0258002772
Email
piergiuseppe.agostoni@ccfm.it
First Name & Middle Initial & Last Name or Official Title & Degree
Elisabetta Salvioni, PhD
Phone
+39-0258002010
Email
elisabetta.salvioni@ccfm.it
Facility Information:
Facility Name
Centro Cardiologico Monzino, Irccs
City
Milano
ZIP/Postal Code
20138
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Piergiuseppe Agostoni
Phone
0258002010
Email
piergiuseppe.agostoni@ccfm.it

12. IPD Sharing Statement

Learn more about this trial

Effect of the Use of Protective Masks on the Ability to Perform Daily Activities in Patients With Heart Failure or Obstructive Pulmonary Disease

We'll reach out to this number within 24 hrs