Efficacy of an Education Protocol in the Correction of Inhalation Techniques in COPD

NCT ID: NCT03144557

Last Updated: 2017-05-09

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

61 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-02

Study Completion Date

2017-04-30

Brief Summary

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This study evaluates the implementation of an education protocol and its impact on the correct inhalation technique in COPD patients presenting errors or mistakes. There will be 4 sessions, in each one the inhalation technique will be evaluated using a checklist of steps. Whenever errors are found, the correct use of each device will be educated through verbal explanation and written material will be delivered.

Detailed Description

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Conditions

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COPD Education

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Intervention

Education protocol to correct inhalation technique

Group Type EXPERIMENTAL

Education

Intervention Type OTHER

Education protocol included 4 individual sessions of verbal and graphic instructions to correct inhalation technique in patients with COPD

Interventions

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Education

Education protocol included 4 individual sessions of verbal and graphic instructions to correct inhalation technique in patients with COPD

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients with COPD diagnosed by spirometry (presence of a postbronchodilator FEV1 / FVC ratio \<0.7)
* Over 40 years old
* Use any of the following devices: metered dose inhaler, HandiHaler, Turbuhaler, Diskus, Aerolizer
* Have at least one error in the inhalation technique
* Signature of informed consent.

Exclusion Criteria

* Artificial airway
* Cognitive impairment noted in the medical history
* Hearing loss that complicates the compression of simple orders
* Bilateral amaurosis
* Functional dependence for the use of inhalers
* Presence of abnormal movements in the upper limbs that interfere and / or impede the correct use of the devices
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospital Italiano de Buenos Aires

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Guadalupe Gracia, PT-RT

Role: PRINCIPAL_INVESTIGATOR

Hospital Italiano de Buenos Aires

Locations

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Hospital Italiano de Buenos Aires

Buenos Aires, , Argentina

Site Status

Countries

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Argentina

References

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Other Identifiers

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3064

Identifier Type: -

Identifier Source: org_study_id

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