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Chronic Obstructive Pulmonary Disease (COPD) and Advance Directives (DIABPCO)

H

Hôpital NOVO

Status

Completed

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Behavioral: Advance directives

Study type

Observational

Funder types

Other

Identifiers

NCT04459143
CHRD 0918

Details and patient eligibility

About

The aim of this study is to evaluate if the participation of COPD patients to a workshop on advance directives increases the number of patients who write them.

Full description

Chronic Obstructive Disease is a common disease and should be the third leading cause of death in 2020. Patient hospitalized for an exacerbation of their COPD have a median survival of 2 years and 50% risk of being rehospitalized within 6 months.

COPD patients may have symptoms that impair their life quality significantly and sometimes more than patients with cancer. This is particularly the case for dyspnea, which is frequently present.

In the study, Investigators propose the setting up of health workshop on advance directives. This workshop is for sever or very severe COPD patients during their hospital stay in the post-acute care and pulmonary rehabilitation service.

In this unit, investigators welcome patient from all the region of Ile de France for a hospital stay of approximately 6 weeks. A first workshop will take place during the third week of their care to inform them about COPD, exacerbations, prognostic and advance directives. Then, a personal interview with patients who have participated to this workshop will take place to collect their advance directives and their degree of satisfaction about this process.

Enrollment

525 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • COPD Gold 3 or 4 and Curtis criteria

Exclusion criteria

  • left to the discretion of the investigator if he finds that it will not be beneficial for the patient : for example if the workshop is judged to be at risk of being anxiety-provoking

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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