Multiparametric Telemonitoring In Elderly People With Chronic Heart Failure
Primary Purpose
Heart Failure
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Telemonitoring
Standard care
Sponsored by
About this trial
This is an interventional health services research trial for Heart Failure
Eligibility Criteria
Inclusion Criteria:
- Patients with heart failure
Exclusion Criteria:
- Cognitive impairment precluding the use of the experimental device
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Telemonitoring + Standard care
Standard care
Arm Description
Outcomes
Primary Outcome Measures
Hospital admissions or death
Rate of hospital admissions for any reason or death
Secondary Outcome Measures
Acute heart failure events
Rate of acute heart failure, defined as a worsening of the patient's condition that necessitates a change in regular medications
Full Information
NCT ID
NCT01914588
First Posted
July 25, 2013
Last Updated
July 31, 2013
Sponsor
Campus Bio-Medico University
1. Study Identification
Unique Protocol Identification Number
NCT01914588
Brief Title
Multiparametric Telemonitoring In Elderly People With Chronic Heart Failure
Official Title
Effectiveness of a Multiparametric Telemonitoring System on Prevention of Hospital Admissions and Mortality In Elderly People With Chronic Heart Failure
Study Type
Interventional
2. Study Status
Record Verification Date
July 2013
Overall Recruitment Status
Completed
Study Start Date
June 2012 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
July 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Campus Bio-Medico University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Heart failure is a chronic disease associated with an increasing risk of morbidity, disability, repeated hospitalizations and mortality. Telemedicine could promptly identify signs of worsening cardiac disease in order to improve elderly patients' home care and quality of life by reducing the need of hospital admissions and sanitary costs. The investigators present a randomized, parallel-group trial to test the ability of a multiparametric remote monitoring system, in addition to standard care, to promptly identify worsening of heart failure and prevent hospital admission and mortality.
Detailed Description
The participants were recruited in two settings:
Patients discharged with a first diagnosis of heart failure from the Geriatric Acute Care ward of a teaching hospital ("Policlinico Campus Bio-Medico", Rome, Italy);
Patients with a principal diagnosis of heart failure attending the outpatients clinic of the same hospital.
All the participants were evaluated at baseline and at the end of the study using a multi-dimensional assessment including well validated and routinely used tools to screen geriatric patients in order to detect global, physical and instrumental autonomy and consequent degree of dependence, as well as cognitive status. The assessment tool included: Activities of daily living scale (ADL) and Instrumental activities of daily living scale (IADL); Abbreviated mental Test; Geriatric Depression Scale; Physical Activity Scale for the Elderly; Six-minute walking test; The Short Form Health Survey (SF-12); Cumulative Illness Rating Scale (CIRS); complete list of drugs.
Once written consent form was obtained, participants were allocated to the study groups in a 1:1 ratio using a computer-generated random list of number.
Participants were followed up for six months. Patients in the intervention group were monitored via a system called PHEBO (Platform for High tech Evaluation of Biometrics Observation) that consisted of a commercial Android-based smartphone and a kit of measurement instruments (sphygmomanometer, pulse oximeter and an electronic scale) with a bluetooth transmitter.
The smartphone received via bluetooth the readings from the measurement instruments, communicated in real-time the readings to the central component of the system and issued reminders for the patient when measurement was scheduled.
Patients in the telemonitoring group received a training session during which they were instructed on how to use the monitoring system and how to perform measurements in case of symptoms. At the end of the session correct comprehension of the system functioning was tested for each patient. A study physician was available on call during office hours to assist patients needing further instructions. A technician was also available in order to solve ingoing hardware malfunctioning. Participants unable to properly use the kit were excluded from the study.
The kit was able to record peripheral oxygen saturation, heart rate, systolic, diastolic and average blood pressure, body weight, average physical activity. We set a specific schedule of the measurements:
Blood pressure and heart rate: three times a day
Peripheral oxygen saturation: three times a day
Body weight: once a day
Physical activity: recorded continuously.
The data received were evaluated every day by a geriatrician. The monitor system displayed an alert when a measurement was outside a predetermined range. In case of abnormal readings, the physician contacted the patient to verify whether their symptoms had worsened or new symptoms had arose. In this event, the patient's adherence to therapy was checked and, if unsatisfactory, individually tailored interventions promoting adherence were carried up. Otherwise, an once appointment (for patients with milder abnormalities or symptoms) or a hospital admission was scheduled.
Participants not included in the intervention group received standard care. In particular, patients discharged from the acute care ward received detailed instruction about medical therapy and lifestyle counselling. A follow-up visit was scheduled at 1 month after the discharge. A geriatrician was available for telephonic support from Monday to Friday, two hours/day. Patients enrolled in the ambulatory setting were followed by planned visits and by their general practitioner.
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
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Telemonitoring + Standard care
Arm Type
Experimental
Arm Title
Standard care
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Telemonitoring
Intervention Description
Use of wearable sensors able to record peripheral oxygen saturation, heart rate, systolic, diastolic and average blood pressure, body weight, average physical activity, with automatic transmission to the monitoring central.
Intervention Type
Other
Intervention Name(s)
Standard care
Intervention Description
Detailed instruction about medical therapy and lifestyle counseling
Telephonic support by a geriatrician, available from Monday to Friday, two hours/day
Follow-up visits
Primary Outcome Measure Information:
Title
Hospital admissions or death
Description
Rate of hospital admissions for any reason or death
Time Frame
Six months
Secondary Outcome Measure Information:
Title
Acute heart failure events
Description
Rate of acute heart failure, defined as a worsening of the patient's condition that necessitates a change in regular medications
Time Frame
Six months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with heart failure
Exclusion Criteria:
Cognitive impairment precluding the use of the experimental device
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raffaele Antonelli Incalzi, MD
Organizational Affiliation
Campus Bio-Medico University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Multiparametric Telemonitoring In Elderly People With Chronic Heart Failure
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