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Telehealth Program in Chronic Patients

Primary Purpose

Pulmonary Disease, Chronic Obstructive, Heart Failure

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Home-based telehealth program
Home-based rehabilitation
Usual care
Sponsored by
Fondazione Salvatore Maugeri
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Pulmonary Disease, Chronic Obstructive focused on measuring Telehealth, Home-based, rehabilitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • COPD new GOLD classification (B, C and D class) and a spirometry in the previous year and
  • Systolic and/or diastolic CHF defined at least by an echocardiogram performed in clinical stability; II, III and IV New York Heart Association class and optimized drug therapy.
  • Informed consent signed

Exclusion Criteria:

  • Physical activity limitations caused by non-cardiac and/or pulmonary problems
  • Obstructive Cardiomyopathies and/or myocarditis
  • Non cardiac and/or pulmonary pathologies that would cause the death of the patient during the study
  • Poor adherence and compliance of the patient

Sites / Locations

  • FSM Respiratory Unit
  • Fondazione Salvatore Maugeri, Cardiology Unit
  • Fondazione Salvatore Maugeri, Telemedicine Service

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Control group (Group A)

Intervention group (Group B)

Arm Description

The patients will be followed in the usual care manner by GPs and by routine specialist visits, if needed

Group B (Home-based intervention): the patients will be followed at home for 4 months by nurse and therapist and will perform an individual rehabilitative program. The interventions will be: Home-based telehealth program Home-based rehabilitation

Outcomes

Primary Outcome Measures

Improvement tolerance capacity
The improvement in tolerance capacity will be measured by walking test performance (meters walked)

Secondary Outcome Measures

Reduction of hospitalisations for cardiovascular disease and /or respiratory disease
Reduction of hospitalisations for all-cases
energy expenditure and duration and quantification of physical activity Energy expenditure and duration and quantification of physical activity
The outcome will be measured in a subgroup of patients using metabolic holter monitoring using the Body Monitoring Multi-Sensor Armband (BMSA) (SenseWear) worn at the triceps of the right arm for at least 72 h.
Improvement of quality of life
The improvement in quality of life, measured by Minnesota Questionnaire and CAT
Reduction of clinical instabilities without hospital admission
The reduction of clinical instabilities will be measured by number of times that patients need to use antibiotics and/or corticosteroids and/or number of times that patients need to increase dosage of diuretic
Reduction of impairment/disability
The reduction of impairment/disability will be measured with Barthel index
Adherence to at least 70% proposal rehabilitative sessions
The adherence will be calculated only in the group B

Full Information

First Posted
October 17, 2014
Last Updated
February 5, 2016
Sponsor
Fondazione Salvatore Maugeri
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1. Study Identification

Unique Protocol Identification Number
NCT02269618
Brief Title
Telehealth Program in Chronic Patients
Official Title
Innovative Multidisciplinary Telehealth Program in COPD and CHF Patients: a Randomized Control Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
June 2013 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fondazione Salvatore Maugeri

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this randomized control study is to determine the feasibility and efficacy of an innovative multidisciplinary telehealth program in chronic obstructive pulmonary disease (COPD) and chronic heart failure (CHF) patients. 120 patients (1:1) will be included in the study and followed for 4 months and for additional 2 months of follow-up. The primary outcome is to improve tolerance capacity
Detailed Description
COPD and CHF frequently coexist, causing a significant worsening in the quality of life of the patients and increasing morbidity and mortality. The prevalence of COPD in the CHF patients ranges from 20% to 32% of cases, and CHF is prevalent in more than 20% of patients with COPD. COPD and CHF patients are complicated and frail with a high risk of re-hospitalizations; for this reason an individualized and multidisciplinary program need to be implemented in these patients. The chronic disease trend is fluctuating, burdened by many exacerbations through a vicious circle with dyspnoea, decreased activity, new exacerbations, depression and social isolation, leading to death. The weight of evidence from a meta-analysis of randomized trials indicates that a multidisciplinary disease-management approach has the best outcomes in terms of prolonged survival and reduced hospital-readmission rates. Home-based management might, arguably, be the preferred approach after hospitalization of chronic diseases patients. Home-base management might provide an opportunity to prevent clinical deterioration and hospitalizations by a comprehensive, long-term intervention with regular reinforcement of patient adherence, knowledge, and skills. A personalized hospital-discharge programme seems to be the best approach to plan the follow-up care of patients with chronic diseases. These programmes, particularly important in the care of patients with multiple comorbidities, should include a routine self-management support, consisting in education to recognize symptoms early, to manage medical devices, to identify barriers to adherence to therapy such as adverse effects of drugs, and to check that the intensity of physical therapy is appropriate. Our study want to investigate feasibility and efficacy of a multidisciplinary telehealth and tele-rehabilitation home based program in patients with COPD and CHF. This is an integrated, multidisciplinary nurse and therapist oriented program; these two figures have a central role during home based intervention and became an essential interface in the dialogue between patient and specialist. The nurse and therapist, each for their competence, collect information, carry out education and training, verify adherence to drug and physical therapy, verify the quality of caregiver assistance. When needed, they require intervention of specialist for consultation or second-opinion. After drug therapy optimization and physical rehabilitation program definition, the patient will be allocated randomly into 2 groups: 1. Group A (usual care): the patients will be followed in the usual care manner by General Practitioner (GP) and routine specialist visits. 2. Group B (Home-based intervention): the patients will be monitored at home for 4 months by nurse and therapist and they will perform an individual rehabilitative program including at least 3 sessions/week of mini-ergometer and exercises and 2 sessions/week of walking with pedometer. At baseline, after 4 months and further 2 months of follow-up all patients in both groups will undergo to follows clinical and physical evaluations: ECG (T0; T4 if needed) Echocardiogram (T0, T4 if needed Spirometry (T0 or a spirometry available in the previous year) Arterial blood gases (T0; T4) Walking test (T0; T4; T6) Metabolic Holter monitoring using the Body Monitoring Multi-Sensor Armband (BMSA) (SenseWear) worn at the triceps of the right arm for at least 72 h. (T0; T4; T6) The questionnaires and scale : Minnesota (T0;T4;T6) COPD Assessment Test (CAT) (T0;T4;T6) Barthel (T0;T4;T6) Dyspnoea and muscle fatigue by Borg scale evaluation, referred by patient during his regular day (T0;T4;T6) Medical Research Council (MRC) scale for dyspnoea during regular day (T0;T4;T6) Physical activity scale for the elderly (PASE) (T0;T4;T6) Customer satisfaction (T4, only group B)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive, Heart Failure
Keywords
Telehealth, Home-based, rehabilitation

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
113 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group (Group A)
Arm Type
Active Comparator
Arm Description
The patients will be followed in the usual care manner by GPs and by routine specialist visits, if needed
Arm Title
Intervention group (Group B)
Arm Type
Other
Arm Description
Group B (Home-based intervention): the patients will be followed at home for 4 months by nurse and therapist and will perform an individual rehabilitative program. The interventions will be: Home-based telehealth program Home-based rehabilitation
Intervention Type
Other
Intervention Name(s)
Home-based telehealth program
Intervention Description
Home-based telehealth program Scheduled calls initiated by nurse performed weekly; the nurse carried out a standardized interview on general clinical condition of the patients. Unscheduled calls initiated by patients or caregivers through the service centre(24h/24h) to report any clinical problems. in case of signs or symptoms Telemonitoring: during calls, patients can transmit via landline or mobile phone the recordings from the 1-lead ECG to a service centre, and talk to the nurse or doctor Home visit performed by therapist seven days after hospital discharge by setting the daily physical activity and other home visits in case of need Scheduled calls initiated by therapist performed weekly aimed at increasing workload and evaluating the proper execution of exercises.
Intervention Type
Other
Intervention Name(s)
Home-based rehabilitation
Intervention Description
Home-based rehabilitation Individual rehabilitative program including at least 3 sessions/week of mini-ergometer and exercises and 2 sessions/week of walking with pedometer Mini-ergometer: The personalized protocol will be structured at the beginning on the basis of data obtained from the assessment of the baseline exercise test, trying to get a training activity to the maximum value of around a Borg dyspnoea and motor equal to 6 (according to the protocol of Maltais) Walking: The patient will be encouraged to walk every day. Will be given a pedometer and will be asked to try to increase the amount of steps up to the maximal for the patient.
Intervention Type
Other
Intervention Name(s)
Usual care
Intervention Description
Usual care All patients will be followed also in usual care manner by their GPs.
Primary Outcome Measure Information:
Title
Improvement tolerance capacity
Description
The improvement in tolerance capacity will be measured by walking test performance (meters walked)
Time Frame
4 months and 6 months
Secondary Outcome Measure Information:
Title
Reduction of hospitalisations for cardiovascular disease and /or respiratory disease
Time Frame
4 months
Title
Reduction of hospitalisations for all-cases
Time Frame
4 months
Title
energy expenditure and duration and quantification of physical activity Energy expenditure and duration and quantification of physical activity
Description
The outcome will be measured in a subgroup of patients using metabolic holter monitoring using the Body Monitoring Multi-Sensor Armband (BMSA) (SenseWear) worn at the triceps of the right arm for at least 72 h.
Time Frame
4 months and 6 months
Title
Improvement of quality of life
Description
The improvement in quality of life, measured by Minnesota Questionnaire and CAT
Time Frame
4 months
Title
Reduction of clinical instabilities without hospital admission
Description
The reduction of clinical instabilities will be measured by number of times that patients need to use antibiotics and/or corticosteroids and/or number of times that patients need to increase dosage of diuretic
Time Frame
4 months
Title
Reduction of impairment/disability
Description
The reduction of impairment/disability will be measured with Barthel index
Time Frame
4 months
Title
Adherence to at least 70% proposal rehabilitative sessions
Description
The adherence will be calculated only in the group B
Time Frame
4 months and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: COPD new GOLD classification (B, C and D class) and a spirometry in the previous year and Systolic and/or diastolic CHF defined at least by an echocardiogram performed in clinical stability; II, III and IV New York Heart Association class and optimized drug therapy. Informed consent signed Exclusion Criteria: Physical activity limitations caused by non-cardiac and/or pulmonary problems Obstructive Cardiomyopathies and/or myocarditis Non cardiac and/or pulmonary pathologies that would cause the death of the patient during the study Poor adherence and compliance of the patient
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michele Vitacca, MD
Organizational Affiliation
Fondazione Salvatore Maugeri
Official's Role
Study Chair
Facility Information:
Facility Name
FSM Respiratory Unit
City
Lumezzane
State/Province
BS
ZIP/Postal Code
25066
Country
Italy
Facility Name
Fondazione Salvatore Maugeri, Cardiology Unit
City
Lumezzane
State/Province
BS
Country
Italy
Facility Name
Fondazione Salvatore Maugeri, Telemedicine Service
City
Lumezzane
State/Province
BS
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
19168510
Citation
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Results Reference
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PubMed Identifier
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Citation
Macchia A, Monte S, Romero M, D'Ettorre A, Tognoni G. The prognostic influence of chronic obstructive pulmonary disease in patients hospitalised for chronic heart failure. Eur J Heart Fail. 2007 Sep;9(9):942-8. doi: 10.1016/j.ejheart.2007.06.004. Epub 2007 Jul 12.
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
22694996
Citation
Walters JA, Cameron-Tucker H, Courtney-Pratt H, Nelson M, Robinson A, Scott J, Turner P, Walters EH, Wood-Baker R. Supporting health behaviour change in chronic obstructive pulmonary disease with telephone health-mentoring: insights from a qualitative study. BMC Fam Pract. 2012 Jun 13;13:55. doi: 10.1186/1471-2296-13-55.
Results Reference
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PubMed Identifier
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Citation
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Citation
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PubMed Identifier
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Citation
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Citation
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Results Reference
derived

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Telehealth Program in Chronic Patients

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