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Tele-spirometry in Primary Care-Randomized Clinical Trial Cluster:Telemedicine in Chronic Obstructive Pulmonary Disease (RESPIRANET-C)

H

Hospital de Clinicas de Porto Alegre

Status

Unknown

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Other: teleconsultation
Other: telemonitoring
Other: Spirometry - 20 weeks
Other: Spirometry

Study type

Interventional

Funder types

Other

Identifiers

NCT02901535
227190 COPD

Details and patient eligibility

About

The purpose of this study is to determine the effectiveness of telemedicine multifaceted intervention in symptoms patients with chronic obstructive pulmonary disease.

Full description

This study is a randomized clinical trial for patients with chronic obstructive pulmonary disease from a primary care. The purpose is to determine the effectiveness of telemedicine (teleconsultation and telemonitoring) in control of chronic obstructive pulmonary disease symptoms.

Enrollment

240 estimated patients

Sex

All

Ages

12 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • spirometry from TelessaudeRS-Universidade Federal do Rio Grande do Sul (from randomization cluster), Modified Medical Research Council Dyspnea > 0

Exclusion criteria

  • normal or restrictive spirometry, low quality spirometries (inadequate)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

240 participants in 2 patient groups

Control
Active Comparator group
Description:
Spirometry in baseline Spirometry - 20 weeks
Treatment:
Other: Spirometry - 20 weeks
Other: Spirometry
Intervention
Experimental group
Description:
Spirometry in baseline Teleconsultation Telemonitoring Spirometry - 20 weeks
Treatment:
Other: Spirometry - 20 weeks
Other: teleconsultation
Other: telemonitoring
Other: Spirometry

Trial contacts and locations

1

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Central trial contact

Cynthia G Molina-Bastos, MD; Marcelo R. Gonçalves, PhD

Data sourced from clinicaltrials.gov

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