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Remote Monitoring of Patients With COPD

V

Vastra Gotaland Region

Status

Completed

Conditions

COPD

Treatments

Other: Normal Care
Device: Telemonitoring

Study type

Interventional

Funder types

Other

Identifiers

NCT03558763
MONITOR

Details and patient eligibility

About

This clinical investigation will evaluate the patient-equipment interface and patient preference in the use of modern possibilities for remote monitoring of patients with COPD in a personalized care approach.

Full description

The primary objective is to evaluate the impact and feasibility of tele monitoring and video contact in personalized care of moderate and severe COPD patients. This should be compared to normal standards of care. The cross-over design evaluates the influence on general HRQOL of this tablet and monitoring system.

Enrollment

70 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Willingness to participate and provision of informed consent
  • Diagnosis of COPD
  • FEV1/FVC (post bronchodilator) <0.7
  • GOLD severity grade D
  • FEV, < 80% predicted
  • Cognitive ability relevant for the studies as judged by the investigator
  • Living in their own home and able to manage their activities of daily living

Exclusion criteria

  • Rapidly progressing severe disease other than COPD and COPD-related diseases, influencing the Health-Related Quality of Life (HRQOL) during the study time as judged by the investigator
  • Long-term stay ( >2 weeks) away from home during the study period, where there are no possibility to get internet connection
  • COPD exacerbation during 1 month before start of study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Normal Care
Active Comparator group
Description:
During normal care the subjects will get the possibility to call the COPD-center via telephone on their own initiative e g with worsening symptoms as usual.
Treatment:
Other: Normal Care
Telemonitoring
Active Comparator group
Description:
Twice a week subject will perform additional vital functions: Blood pressure and heart rate will be measured using the Electronic Sphygmomanometers "Track". Weight will be taken using the Scale "lite" Oxygen saturation will be measured using Pulse Oximeter "Air" And Complete two PRO´s (integrated in the application): CAT MRC All this is estimated to take approximately 20-30 min each time. For the first 4 weeks there will be weekly video calls with a COPD-center nurse discussing health condition and vital parameters. Thereafter there will be monthly video calls with a COPD-center nurse for the remaining 5 months, i.e. 4 further calls. The video calls will take approximately 15 min.
Treatment:
Device: Telemonitoring

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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