Home BIA Management System in Patients With Heart Failure
Primary Purpose
Heart Failure,Congestive
Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Preemptive management using home BIA monitoring system
Sponsored by
About this trial
This is an interventional prevention trial for Heart Failure,Congestive focused on measuring Heart failure, Bioelectrical impedance analysis
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed heart failure
- Patients taking loop diuretics for HF symptom control
- Patients who can use a smart-phone
Exclusion Criteria:
- Patients with implanted devices that could interfere with the BIA such as ICD and CRT
- Patients with limb defects
- Patients who unable to stand alone
- Patients who are pregnant
- Patients with End-stage renal disease (ESRD) on hemodialysis, serum creatinine of more than 5mg/dL, or nephritic syndrome
- Patients with systemic diseases such as hypothyroidism, decompensated liver cirrhosis, and systemic lupus erythematosus.
- Patients with active cellulitis, severe varicose vein, deep vein thrombosis or lymphedema
Sites / Locations
- Soonchunhyang University Bucheon HospitalRecruiting
- Korea University Guro HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Home BIA Monitoring group
Control group
Arm Description
Preemptive management by Body fluid monitoring system (BWA ON + App + Web)
Usual heart failure management (Outpatient follow-up and medical treatment)
Outcomes
Primary Outcome Measures
Change from baseline in NT-proBNP
NT-proBNP
Secondary Outcome Measures
Rate of heart failure hospitalizations (HHF)
Hospitalization for heart failure
Change from baseline in edema index using BIA
Edema index by BIA
Change from baseline in Creatinine
Creatinine
Change from baseline in symptom of dyspnea
NYHA classification and VAS scale of dyspnea
Full Information
NCT ID
NCT05177081
First Posted
January 3, 2022
Last Updated
January 3, 2022
Sponsor
Korea University Guro Hospital
Collaborators
Soonchunhyang University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05177081
Brief Title
Home BIA Management System in Patients With Heart Failure
Official Title
Feasibility of Treatment Using Home Bioelectrical Impedance Analysis and Linked Application System in Patients With Heart Failure: A Multicenter Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 23, 2021 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Korea University Guro Hospital
Collaborators
Soonchunhyang University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is a prospective, multi-center, open label, randomized clinical trial conducted in the republic of Korea. The objective of this study is to evaluate the efficacy and safety of the treatment using home bioelectrical impedance analysis (BIA) and linked application system in patients with heart failure (HF).
Detailed Description
The prevalence of HF is generally estimated at 1% to 2% of the general population. The more concerning thing is that HF patients are rapidly increasing due to an increase of elderly population derived from life extension; an increase in the number of survivors of heart disease due to the development of medical technology; and an increase in risk factors for HF such as obesity, diabetes, and ischemic heart disease.
HF is known that a quarter of HF patients are readmitted within 1 year, and the mortality rate within 5 years is about 50%. HF is a chronic condition, punctuated by acute decompensated episodes. Each acute decompensated event results in further organ damage: myocardial and renal damage occurring during such episodes may contribute to progressive left ventricular and/or renal dysfunction. Increasing frequency of acute events with disease progression leads to higher rates of hospitalization and increased risk of mortality.
The main symptoms of HF are shortness of breath and swelling, which are the main reasons for visiting the emergency room and hospitalization. After discharge, body water monitoring and management of HF patients are very important to prevent HF aggravation and re-hospitalization.
There are several methods of body fluid monitoring in HF patients. Current guidelines of heart failure recommends monitoring of pulmonary artery pressures using a wireless implantable hemodynamic monitoring system in symptomatic HF patients with previous HF hospitalization. Multi-parameter monitoring based on ICD is also recommended in order to improve clinical outcomes in HF patients. However, existing HF monitoring and management systems have limitations of its invasiveness, expensive costs and a lot of medical providers' efforts. Other body water monitoring methods are signs and symptoms monitoring and body weight-based monitoring. However, signs such as weight gain and edema or symptoms like dyspnea due to worsening heart failure were not recognized until just 7 and 3 days before the hospitalization event.
BIA, Bioelectrical impedance analysis can be a novel option for body water monitoring method in HF patients. Nowadays, it is possible to obtain more accurate body water by reflecting both intracellular and extracellular water by using multiple frequencies, and it is possible to accurately measure body water even in patients with unusual body water conditions such as heart failure status. Moreover, the changes of Bioelectrical Impedance are detected about two weeks before heart failure hospitalization. It is the key benefit for congestion monitoring and management.
Previous studies have shown that monitoring body water through non-invasive bioelectrical impedance can predict the worsening of HF even in patients with heart failure. In addition, there are studies that reported improvement of clinical results during treatment based on the edema index (extracellular water / total body water) during body water monitoring through non-invasive bioelectrical impedance.
Home BIA monitoring using BWA-ON has potential benefit for continuous water monitoring for edema control in patients with HF. Therefore, we aim to evaluate feasibility of treatment using home BIA and linked application system in patients with heart failure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure,Congestive
Keywords
Heart failure, Bioelectrical impedance analysis
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
multi-center, open label, randomized trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Home BIA Monitoring group
Arm Type
Experimental
Arm Description
Preemptive management by Body fluid monitoring system (BWA ON + App + Web)
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Usual heart failure management (Outpatient follow-up and medical treatment)
Intervention Type
Device
Intervention Name(s)
Preemptive management using home BIA monitoring system
Intervention Description
Patients check their body composition and fluid using Home BIA system. Investigators analyze patients' body congestion status and send patient's edema status and direction of extra-diuretics usage to enrolled patients every one week.
Primary Outcome Measure Information:
Title
Change from baseline in NT-proBNP
Description
NT-proBNP
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Rate of heart failure hospitalizations (HHF)
Description
Hospitalization for heart failure
Time Frame
3 months
Title
Change from baseline in edema index using BIA
Description
Edema index by BIA
Time Frame
3 months
Title
Change from baseline in Creatinine
Description
Creatinine
Time Frame
3 months
Title
Change from baseline in symptom of dyspnea
Description
NYHA classification and VAS scale of dyspnea
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed heart failure
Patients taking loop diuretics for HF symptom control
Patients who can use a smart-phone
Exclusion Criteria:
Patients with implanted devices that could interfere with the BIA such as ICD and CRT
Patients with limb defects
Patients who unable to stand alone
Patients who are pregnant
Patients with End-stage renal disease (ESRD) on hemodialysis, serum creatinine of more than 5mg/dL, or nephritic syndrome
Patients with systemic diseases such as hypothyroidism, decompensated liver cirrhosis, and systemic lupus erythematosus.
Patients with active cellulitis, severe varicose vein, deep vein thrombosis or lymphedema
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eung Ju Kim, MD, PhD
Phone
82-2-26263022
Email
withnoel@empas.com
First Name & Middle Initial & Last Name or Official Title & Degree
Min Gyu Kong, MD
Phone
82-31-621-6727
Email
mingyu.kong@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eung Ju Kim, MD, PhD
Organizational Affiliation
Korea University Guro Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Soonchunhyang University Bucheon Hospital
City
Bucheon-si
State/Province
Gyeonggi-do
ZIP/Postal Code
14584
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Min Gyu Kong, MD
Phone
82-31-621-6727
Email
mingyu.kong@gmail.com
Facility Name
Korea University Guro Hospital
City
Seoul
ZIP/Postal Code
08308
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eung Ju Kim, MD, PhD
Phone
82-2-2626-3022
Email
withnoel@empas.com
12. IPD Sharing Statement
Plan to Share IPD
No
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Home BIA Management System in Patients With Heart Failure
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