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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	ClinicalTrials.gov
Last refreshed on:	16 December 2017
Main ID:	NCT02901535
Date of registration:	12/09/2016
Prospective Registration:	No
Primary sponsor:	Hospital de Clinicas de Porto Alegre
Public title:	Tele-spirometry in Primary Care-Randomized Clinical Trial Cluster:Telemedicine in Chronic Obstructive Pulmonary Disease RESPIRANET-C
Scientific title:	Tele-spirometry in Primary Care - Randomized Clinical Trial Cluster: the Effectiveness of Multifaceted Intervention in Symptoms Patients With Respiratory Illness
Date of first enrolment:	April 2015
Target sample size:	240
Recruitment status:	Recruiting
URL:	https://clinicaltrials.gov/show/NCT02901535
Study type:	Interventional
Study design:	Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Investigator).
Phase:	N/A

Countries of recruitment
Brazil

Contacts

Name:	Marcelo R. Gonçalves, PhD
Address:
Telephone:	5191175156
Email:	marcelorog@gmail.com
Affiliation:

Name:	Cynthia G Molina-Bastos, MD
Address:
Telephone:	5191322585
Email:	cyncarol@gmail.com
Affiliation:

Name:	Erno Harzheim, PhD
Address:
Telephone:
Email:
Affiliation:	Federal University of Rio Grande do Sul

Key inclusion & exclusion criteria

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)

Age minimum: 12 Years
Age maximum: 100 Years
Gender: All

Health Condition(s) or Problem(s) studied

Chronic Obstructive Pulmonary Disease

Intervention(s)

Other: Spirometry - 20 weeks

Other: teleconsultation

Other: telemonitoring

Other: Spirometry

Primary Outcome(s)

Symptoms [Time Frame: 20 a 22 weeks]

Secondary Outcome(s)

Spirometry - FEV1 [Time Frame: 20 a 22 weeks]

Spirometry - FVC [Time Frame: 20 a 22 weeks]

Secondary ID(s)

227190 COPD

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Programa de Pos-graduação em Epidemiologia - Universidade Federal do Rio Grande do Sul

Ministry of Health, Brazil

TelessaúdeRS-Universidade Federal do Rio Grande do Sul

Ethics review

Results

Results available:
Date Posted:
Date Completed:
URL:

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