Advanced Telemonitoring of Patients With COPD in Home Environment

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-10-14

Study Completion Date

2023-02-01

Brief Summary

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Chronic obstructive pulmonary disease (COPD) is one of the leading and rising causes of morbidity and mortality worldwide. The most important etiopathogenetic agent is smoking. However, air-pollution probably also plays a crucial role in the disease development, progression and exacerbations. The multimodal-telemedicine approach may provide a useful tool in the patient follow-up with the aim to reduce disease exacerbation rate and improve the health-related quality of life. The study aims to investigate the effects and utility of advanced telemonitoring in elderly COPD patients. All data will be integrated in a single web-based platform in order to analyse the mutual effects of different conditions and variables.

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Detailed Description

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Conditions

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COPD

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Medimonitor

A digital solution consisting of smartphone/tablet based application gathering data from medical and other devices provided to the patients. These devices are as follows: tablet, smart inhaler, spirometer, blood pressure monitor, pulse oximetry device, particulate matter sensor.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* COPD
* ≥ 60 years of age
* Informed written and verbal consent
* Ability to participate in study activities

Exclusion Criteria

* Active smoking
* Respiratory failure requiring oxygenotherapy or ventilation support
* Severe psychological disturbances
* Absence of collaboration (informed consent)
* Other comorbid pulmonary disease
* Symptomatic heart failure
* Motor neuron diseases (e.g. amyotrophic lateral sclerosis etc.)

Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No