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Impact of Telemedicine in the Rate of Readmission for COPD. Project CRONEX 3.0

S

Sociedad Española de Neumología y Cirugía Torácica

Status

Completed

Conditions

COPD

Treatments

Other: health care system
Device: Group intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT03505138
CRONEX3.0

Details and patient eligibility

About

The prevalence of COPD is high and suppose one of the first public health problem in the world. It has a high morbidity and mortality and healthcare costs. The economic aspect is directly related to hospitalization, accounting for 45-50% of total expenditure of COPD. Patients with frequent exacerbations generate most of the cost.

In these patients, there are not standardized treatments or monitoring in a medium or long term, but it seems reasonable that the combination of various interventions (programs self-care, active role of health professionals in consultations, home programs, group visits, establishment action plans for patients, use of communication technologies or social networks) may improve many patient outcomes.

The hypothesis of our work will be to introduce telemedicine platform to establish action plans for the patient, recognition of symptoms and exacerbations, treatments for the exacerbations, training material on COPD, smoking and inhalation therapy, establishment of a fast and fluid communication with pulmonologist, with the purpose of responding to various health problems that patients with COPD (exacerbator phenotype or ACO phenotype) may have. We will study the impact of this tool to reduce the rate income or readmission for the patients with COPD, analyzing it from the perspective of cost-effectiveness.

Enrollment

120 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. COPD, which after evaluation of its clinical history, belonging to exacerbator phenotype (chronic bronchitic / emphysema) or mixed phenotype ("COPD-asthma") readmission (2 or more income in the previous year) and are stable least six weeks before inclusion in the study.
  2. Age over 18 years
  3. The patient or caregiver should be able to use the tablet type telematic tool for tracking and monitoring.

Exclusion criteria

  1. Patients with severe comorbidity grade IV heart failure, renal failure on hemodialysis or active neoplasia
  2. Patients with difficulties phone coverage
  3. Patients with lack of adequate social and family support.
  4. Patients who do not grant informed consent

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 2 patient groups

Group intervention
Experimental group
Description:
Conventional management for COPD will take place in our health care system more telematics intervention.
Treatment:
Device: Group intervention
Group control
Active Comparator group
Description:
Is performed only conventional management of COPD in our health care system.
Treatment:
Other: health care system

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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