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A Study on Ability to Detect Early Deterioration of Heart Failure with Respiratory Instability Telemonitoring - Aided by Innovative Tele-Monitoring Environment To Halt Ongoing Deterioration of Heart Failure: ITMETHOD-HF

Not Applicable
Conditions
Chronic Heart Failure
Registration Number
JPRN-UMIN000027060
Lead Sponsor
Osaka University Graduate School of Medicine, Cardiovascular surgery
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
18
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients who share a bed with other person or pets 2. Patients who are not considered able to measure overnight respiratory due to physical factors or lifestyle factors 3. Patients without spontaneous respiration 4. Patients with chronic respiratory failure or chronic obstructive pulmonary disease 5. Patients must not have started to use CPAP or ASV during sleep within a month 6. Patients whose QOL is limited by malignant tumor or other diseases 7. Patients who have sequela as the result of cerebrovascular disorder 8. Patients diagnosed with dementia 9. Patients who are inability to provide informed consent or doubted for his/her agreement 10. Any other patients who are determined as unsuitable for this study by the investigators

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sensitivity of RSI RSI levels of subjects clinically diagnosed as worsening heart failure by the investigator is decreased (1 day or more that the RSI is less than 20) prior to exacerbation. Specificity of RSI RSI levels of subjects clinically diagnosed stable heart failure by the investigator is not decreased less than 20 on the judgment day.
Secondary Outcome Measures
NameTimeMethod
-Days of RSI decrease (less than 20) preceding exacerbation of heart failure -RSI cutoff value -Malfunctions of home telemonitoring -Inter-day variations in RSI
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