Task-specific Training for Patients With Acute Exacerbation of COPD
NCT ID: NCT06224075
Last Updated: 2024-01-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
68 participants
INTERVENTIONAL
2024-01-15
2024-08-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Task-specific training
Task-specific training
Participants in the intervention group will receive the treatment established for the control group and nursing care based on task-specific training. The intervention was designed with the aim of improving inhaler management in COPD patients. The content of the tasks will be adapted to the different types of devices present in the patient's therapeutic regimen, mainly pressurized cartridge and dry powder devices.
In order to carry out the intervention, several tasks related to education, assessment and/or training will be established with the aim of improving the ability to use the prescribed inhalers. The tasks have been classified into 3 blocks: technique execution, device cleaning and medication administration.
Usual care
All patients will receive standard treatment during their hospital stay (medical and pharmacological care). This treatment will include steroids, antibiotics, inhaled bronchodilators and oxygen therapy. In addition, during hospitalization they may receive diuretics, anticoagulants and cardiovascular treatments if necessary.
Usual care
Usual care
All patients will receive standard treatment during their hospital stay (medical and pharmacological care). This treatment will include steroids, antibiotics, inhaled bronchodilators and oxygen therapy. In addition, during hospitalization they may receive diuretics, anticoagulants and cardiovascular treatments if necessary.
Interventions
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Task-specific training
Participants in the intervention group will receive the treatment established for the control group and nursing care based on task-specific training. The intervention was designed with the aim of improving inhaler management in COPD patients. The content of the tasks will be adapted to the different types of devices present in the patient's therapeutic regimen, mainly pressurized cartridge and dry powder devices.
In order to carry out the intervention, several tasks related to education, assessment and/or training will be established with the aim of improving the ability to use the prescribed inhalers. The tasks have been classified into 3 blocks: technique execution, device cleaning and medication administration.
Usual care
All patients will receive standard treatment during their hospital stay (medical and pharmacological care). This treatment will include steroids, antibiotics, inhaled bronchodilators and oxygen therapy. In addition, during hospitalization they may receive diuretics, anticoagulants and cardiovascular treatments if necessary.
Eligibility Criteria
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Inclusion Criteria
* Over 18 years of age.
* Who wish to participate in the study.
* Who sign the informed consent form.
Exclusion Criteria
* Presence of psychiatric or cognitive disorders, organ failure, cancer and/or inability to cooperate.
* Patients who had experienced exacerbation of COPD in the previous month were also excluded.
18 Years
ALL
No
Sponsors
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Universidad de Granada
OTHER
Responsible Party
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Marie Carmen Valenza
Chair of Physiotherapy
Principal Investigators
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Marie Carmen Valenza, Chair
Role: STUDY_DIRECTOR
Universidad de Granada
Locations
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Faculty of Health Sciences. University of Granada.
Granada, Granada, Spain
Countries
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Central Contacts
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Other Identifiers
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DF0101UG
Identifier Type: -
Identifier Source: org_study_id
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