RESPECT Heart Failure- RESpiratory Pattern Evaluation in Clinical Trials for HF (RESPECT)
Primary Purpose
Heart Failure
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MouthLab Device
Sponsored by
About this trial
This is an interventional other trial for Heart Failure
Eligibility Criteria
Inpatient Sub-Study Eligibility Criteria
Inclusion Criteria
- Adults aged ≥ 18 years old
- Willing and able to provide informed consent
- Admitted within previous 24 hours with HF exacerbation requiring intravenous diuretic therapy (reduced or preserved ejection fraction)
- English speaking
Exclusion Criteria
- Currently on dialysis
- Patients with acute coronary syndrome
- Currently on hospice
Have a heart transplant or left ventricular assist device
- Outpatient Sub-Study Eligibility Criteria
Inclusion Criteria
- Adults aged ≥ 18 years old
- Willing and able to provide informed consent
- Patients presenting to the clinic and not being admitted to the hospital, who have been admitted for a HF exacerbation within the past 6 months, OR patients being discharged from a HF exacerbation related inpatient hospitalization
- For inclusion in Cohort 2, patients must have Boston Scientific pacemaker or defibrillator with Heart Logic capability
- For inclusion in Cohort 3, patients must have implantable CardioMEMS device
- Patients currently on inotropes
- English speaking
Exclusion Criteria
- Currently on dialysis
- Currently on hospice
- Have a heart transplant or left ventricular assist device
Sites / Locations
- WakeMed Health and Hospitals
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Other
Other
Other
Arm Label
Cohort 1
Cohort 2
Cohort 3
Arm Description
Stable outpatients without implantable devices
Stable outpatients with Boston Scientific pacemakers or defibrillators with Heart Logic capability
Stable outpatients with implantable CardioMEMS devices
Outcomes
Primary Outcome Measures
Evaluate trends of respiration rate per minute
Respiration rate measured by breaths taken per minute
Aidar Questionnaire to Evaluate Patient Perception of Heart Failure
The Aidar Questionnaire will be used to determine patient perception of severity of heart failure.
Evaluate trends of temperature measured in Fahrenheit
Temperature
Evaluate trends of pulse rate per minute
Pulse rate
Evaluating the P wave of electrocardiogram in milliseconds
P wave on electrocardiogram will be measured to determine heart rhythm
Evaluating the QRS complex on electrocardiogram in milliseconds
QRS complex will be measured to determine heart rhythm
Evaluating the T wave on electrocardiogram in milliseconds
T wave will be measured to determine heart rhythm
Evaluate trends of blood pressure measured in mm/Hg
Blood pressure
Evaluate trends of blood oxygen saturation (SpO2) in percentage
blood oxygen saturation (SpO2)
Measuring FEV1 (Forced Expiratory Volume) in Liters
Determining Lung Function
Measuring FVC (Forced Vital Capacity) in Liters
Determining Lung Function
Measuring FEV1/FVC as a ratio
Determining Lung Function
Measuring PEF (Peak Expiratory Flow) in Liters/second
Determining Lung Function
Secondary Outcome Measures
Full Information
NCT ID
NCT04757246
First Posted
January 21, 2021
Last Updated
October 20, 2022
Sponsor
WakeMed Health and Hospitals
1. Study Identification
Unique Protocol Identification Number
NCT04757246
Brief Title
RESPECT Heart Failure- RESpiratory Pattern Evaluation in Clinical Trials for HF
Acronym
RESPECT
Official Title
RESPECT Heart Failure- RESpiratory Pattern Evaluation in Clinical Trials for HF
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Withdrawn
Why Stopped
Funding from Sponsor did not come through
Study Start Date
October 2022 (Anticipated)
Primary Completion Date
October 2022 (Anticipated)
Study Completion Date
October 20, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
WakeMed Health and Hospitals
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal is to evaluate the trends in MouthLab parameters (respiration rate, temperature, pulse rate, electrocardiogram rhythm, blood pressure, oxygen saturation heart rate and basic lung function measures) in patients with decompensated heart failure and how these measurements change in response to decongestion. The research will test the ability of the MouthLab device to predict clinical decompensation in patients with known heart failure and to reduce the number of hospital readmissions based on the treatment guided by MouthLab device data.
Detailed Description
Heart failure (HF) is becoming increasingly recognized with an estimated worldwide prevalence of >37.7 million individuals. In the United States alone, there are over 5 million patients with HF which is expected to increase to over 8 million by 2030. Despite advances in medical therapies and technology, HF remains the leading cause of hospitalization among adults and the elderly. By 2030, the medical costs of HF are expected to rise from $20.9 billion to $53.1 billion, with nearly 80% of the projected increased expenses attributes to hospitalization costs. As such, it is imperative to develop new technologies and treatment options to impact the HF epidemic.
The majority of HF hospital admissions are due to volume overload. Stiffened and/or weakened myocardium predisposes patients to the accumulation of extracellular fluid resulting in increased intracardiac filling pressures and symptoms of congestion (edema, dyspnea and orthopnea). Accurate assessment of a patient's volume status remains clinically challenging at times. While there have been technological advances in the outpatient monitoring of volume status through thoracic impedance and pulmonary artery pressure monitoring, there are no validated, non-implantable options for monitoring volume status outside of the physical exam.
Aidar Health's MouthLab device is a non-invasive, hand-held, home monitoring tool that measures multiple medical parameters such as - Temperature, Blood Pressure, Heart Rate, Heart Rate Variability, Pulse Rate, SpO2, single-lead ECG, Respiratory Rate, Breathing Pattern/Respiratory Flow Cycle Morphology, and basic lung functions (FEV1, FVC, FEV1/FVC, PEF) in 30 seconds.
The investigators believe that the MouthLab device holds the potential to identify changes in volume status through measurements such as pulse rate, oxygen saturation, respiratory flow and lung function and accurately predict decompensation in patients with chronic HF. The investigators propose the following outline of clinical studies to evaluate the utility of the MouthLab device in HF.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cohort 1
Arm Type
Other
Arm Description
Stable outpatients without implantable devices
Arm Title
Cohort 2
Arm Type
Other
Arm Description
Stable outpatients with Boston Scientific pacemakers or defibrillators with Heart Logic capability
Arm Title
Cohort 3
Arm Type
Other
Arm Description
Stable outpatients with implantable CardioMEMS devices
Intervention Type
Other
Intervention Name(s)
MouthLab Device
Intervention Description
Use of MouthLab system
Primary Outcome Measure Information:
Title
Evaluate trends of respiration rate per minute
Description
Respiration rate measured by breaths taken per minute
Time Frame
6 months
Title
Aidar Questionnaire to Evaluate Patient Perception of Heart Failure
Description
The Aidar Questionnaire will be used to determine patient perception of severity of heart failure.
Time Frame
6 months
Title
Evaluate trends of temperature measured in Fahrenheit
Description
Temperature
Time Frame
6 months
Title
Evaluate trends of pulse rate per minute
Description
Pulse rate
Time Frame
6 month
Title
Evaluating the P wave of electrocardiogram in milliseconds
Description
P wave on electrocardiogram will be measured to determine heart rhythm
Time Frame
6 months
Title
Evaluating the QRS complex on electrocardiogram in milliseconds
Description
QRS complex will be measured to determine heart rhythm
Time Frame
6 months
Title
Evaluating the T wave on electrocardiogram in milliseconds
Description
T wave will be measured to determine heart rhythm
Time Frame
6 months
Title
Evaluate trends of blood pressure measured in mm/Hg
Description
Blood pressure
Time Frame
6 months
Title
Evaluate trends of blood oxygen saturation (SpO2) in percentage
Description
blood oxygen saturation (SpO2)
Time Frame
6 months
Title
Measuring FEV1 (Forced Expiratory Volume) in Liters
Description
Determining Lung Function
Time Frame
6 months
Title
Measuring FVC (Forced Vital Capacity) in Liters
Description
Determining Lung Function
Time Frame
6 months
Title
Measuring FEV1/FVC as a ratio
Description
Determining Lung Function
Time Frame
6 months
Title
Measuring PEF (Peak Expiratory Flow) in Liters/second
Description
Determining Lung Function
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inpatient Sub-Study Eligibility Criteria
Inclusion Criteria
Adults aged ≥ 18 years old
Willing and able to provide informed consent
Admitted within previous 24 hours with HF exacerbation requiring intravenous diuretic therapy (reduced or preserved ejection fraction)
English speaking
Exclusion Criteria
Currently on dialysis
Patients with acute coronary syndrome
Currently on hospice
Have a heart transplant or left ventricular assist device
Outpatient Sub-Study Eligibility Criteria
Inclusion Criteria
Adults aged ≥ 18 years old
Willing and able to provide informed consent
Patients presenting to the clinic and not being admitted to the hospital, who have been admitted for a HF exacerbation within the past 6 months, OR patients being discharged from a HF exacerbation related inpatient hospitalization
For inclusion in Cohort 2, patients must have Boston Scientific pacemaker or defibrillator with Heart Logic capability
For inclusion in Cohort 3, patients must have implantable CardioMEMS device
Patients currently on inotropes
English speaking
Exclusion Criteria
Currently on dialysis
Currently on hospice
Have a heart transplant or left ventricular assist device
Facility Information:
Facility Name
WakeMed Health and Hospitals
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27610
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30700139
Citation
Benjamin EJ, Muntner P, Alonso A, Bittencourt MS, Callaway CW, Carson AP, Chamberlain AM, Chang AR, Cheng S, Das SR, Delling FN, Djousse L, Elkind MSV, Ferguson JF, Fornage M, Jordan LC, Khan SS, Kissela BM, Knutson KL, Kwan TW, Lackland DT, Lewis TT, Lichtman JH, Longenecker CT, Loop MS, Lutsey PL, Martin SS, Matsushita K, Moran AE, Mussolino ME, O'Flaherty M, Pandey A, Perak AM, Rosamond WD, Roth GA, Sampson UKA, Satou GM, Schroeder EB, Shah SH, Spartano NL, Stokes A, Tirschwell DL, Tsao CW, Turakhia MP, VanWagner LB, Wilkins JT, Wong SS, Virani SS; American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2019 Update: A Report From the American Heart Association. Circulation. 2019 Mar 5;139(10):e56-e528. doi: 10.1161/CIR.0000000000000659. No abstract available. Erratum In: Circulation. 2020 Jan 14;141(2):e33.
Results Reference
result
PubMed Identifier
26673558
Citation
Writing Group Members; Mozaffarian D, Benjamin EJ, Go AS, Arnett DK, Blaha MJ, Cushman M, Das SR, de Ferranti S, Despres JP, Fullerton HJ, Howard VJ, Huffman MD, Isasi CR, Jimenez MC, Judd SE, Kissela BM, Lichtman JH, Lisabeth LD, Liu S, Mackey RH, Magid DJ, McGuire DK, Mohler ER 3rd, Moy CS, Muntner P, Mussolino ME, Nasir K, Neumar RW, Nichol G, Palaniappan L, Pandey DK, Reeves MJ, Rodriguez CJ, Rosamond W, Sorlie PD, Stein J, Towfighi A, Turan TN, Virani SS, Woo D, Yeh RW, Turner MB; American Heart Association Statistics Committee; Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2016 Update: A Report From the American Heart Association. Circulation. 2016 Jan 26;133(4):e38-360. doi: 10.1161/CIR.0000000000000350. Epub 2015 Dec 16. No abstract available. Erratum In: Circulation. 2016 Apr 12;133(15):e599.
Results Reference
result
PubMed Identifier
23616602
Citation
Heidenreich PA, Albert NM, Allen LA, Bluemke DA, Butler J, Fonarow GC, Ikonomidis JS, Khavjou O, Konstam MA, Maddox TM, Nichol G, Pham M, Pina IL, Trogdon JG; American Heart Association Advocacy Coordinating Committee; Council on Arteriosclerosis, Thrombosis and Vascular Biology; Council on Cardiovascular Radiology and Intervention; Council on Clinical Cardiology; Council on Epidemiology and Prevention; Stroke Council. Forecasting the impact of heart failure in the United States: a policy statement from the American Heart Association. Circ Heart Fail. 2013 May;6(3):606-19. doi: 10.1161/HHF.0b013e318291329a. Epub 2013 Apr 24.
Results Reference
result
PubMed Identifier
32164892
Citation
Felker GM, Ellison DH, Mullens W, Cox ZL, Testani JM. Diuretic Therapy for Patients With Heart Failure: JACC State-of-the-Art Review. J Am Coll Cardiol. 2020 Mar 17;75(10):1178-1195. doi: 10.1016/j.jacc.2019.12.059.
Results Reference
result
PubMed Identifier
2709167
Citation
Guyatt GH, Nogradi S, Halcrow S, Singer J, Sullivan MJ, Fallen EL. Development and testing of a new measure of health status for clinical trials in heart failure. J Gen Intern Med. 1989 Mar-Apr;4(2):101-7. doi: 10.1007/BF02602348.
Results Reference
result
PubMed Identifier
19052916
Citation
Garin O, Ferrer M, Pont A, Rue M, Kotzeva A, Wiklund I, Van Ganse E, Alonso J. Disease-specific health-related quality of life questionnaires for heart failure: a systematic review with meta-analyses. Qual Life Res. 2009 Feb;18(1):71-85. doi: 10.1007/s11136-008-9416-4. Epub 2008 Dec 4.
Results Reference
result
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RESPECT Heart Failure- RESpiratory Pattern Evaluation in Clinical Trials for HF
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