Comparison of 3 Methods to Assess Inhalation Technique (CINTECH)

February 19, 2023 updated by: Marta Dąbrowska, Medical University of Warsaw

Comparison of Three Methods of Assessment of INhalation TECHnique in Patients With Asthma and COPD

A significant percentage of patients with asthma and COPD do not use their inhalers properly. Experts recommend that in patients with obstructive lung diseases, inhalation technique and patient adherence should be evaluated at every visit. The assessment of inhalation skills depends on the method of evaluation. There are few different methods of assessment of inhalation technique, however none of them is recommended as the most accurate.

Therefore, the aim of the study is:

  1. to compare three different methods of assessment of inhalation technique in patients with asthma and COPD.

    These methods include:

    1. Checklist of mistakes in inhalation technique (including critical mistakes)
    2. 4 grade scale of inhalation technique
    3. Assessment by Vitalograph®AIM (Aerosol Inhaling Monitor)
  2. to analyze the influence of Vitalograph®AIM based inhalation technique training on inhalation skills

One hundred and thirty patients with asthma or COPD, who use inhaled medication on a regular basis will be enrolled. Inhalation technique will be evaluated by two observers independently at the same time with all three methods (checklist, 4 grade scale, Vitalograph®AIM). To compare these methods, the investigators will analyze method reliability and validity. Additionally, inhalation technique will be evaluated 30 minutes after Vitalograph®AIM based training to analyze the potential benefit of its application in practicing inhalation skills.

Study Overview

Status

Completed

Conditions

Detailed Description

Asthma and chronic obstructive pulmonary disease (COPD) are common respiratory diseases. Inhaled therapy is the cornerstone of treatment in these two diseases. However, a significant proportion of patients with asthma and COPD do not use their inhalers properly. Experts recommend that in patients with obstructive lung diseases, inhalation technique and patient adherence should be evaluated at every visit, particularly before introducing changes to the patient's inhalation therapy. The assessment of inhalation skills depends on the method of evaluation. There are few different methods of assessment of inhalation technique, however, none of these methods is recommended as the most accurate.

Therefore, the aim of the study is:

  1. to compare three different methods of assessment of inhalation technique in patients with asthma and COPD.

    These methods include:

    1. Checklist of mistakes in inhalation technique (including critical mistakes)
    2. 4 grade scale of inhalation technique
    3. Assessment by Vitalograph®AIM (Aerosol Inhaling Monitor)
  2. to analyze an influence of using Vitalograph®AIM based inhalation technique training on inhalation skills.

Type of study: prospective, interventional, without randomization. Patients with asthma or COPD treated in hospital or in an out-patient clinic will be asked to participate in the study.

Study design One hundred and thirty patients with asthma or COPD, who use inhaled medication on a regular basis will be enrolled. Inhalation technique will be evaluated by two observers independently at the same time with all three methods (checklist, 4 grade scale, Vitalograph®AIM). To compare these methods, the investigators will analyze method reliability and validity. The reference assessment will be performed by two experienced pulmonologists.

Additionally, inhalation technique will be evaluated 30 minutes after Vitalograph®AIM based training to analyze the potential benefit of its application in practicing inhalation skills.

Outcomes

  1. Comparison of three different methods of assessment of inhalation technique in patients with asthma and COPD (reliability, validity and accuracy)
  2. Difference in the number of mistakes made during inhalation before and after the Vitalograph® AIM based training.

Investigators expect that results of this study will allow to identify the most accurate method for assessment of inhalation technique. Furthermore, the impact of Vitalograph®AIM based training on inhalation skills will be assessed..

Study Type

Interventional

Enrollment (Actual)

120

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Warsaw, Poland, 02-097
        • Department of Internal Medicine, Pneumonology and Allergology, Medical University of Warsaw

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion criteria:

  • informed consent for participating in the study
  • age 18-85 years
  • COPD or asthma diagnosed at least 3 months prior to enrollment
  • using of at least one inhaler regularly every day
  • using one of the inhalers: Metered Dose Inhalers (MDI), Dry Powder Inhalers (DPI) or Metered Dose Liquid Inhalers (MDLI)

Exclusion criteria:

  • lack of informed consent
  • age <18 years or > 85 years
  • diagnosis of asthma or COPD not earlier than 3 months before enrollment
  • using inhalers irregularly.
  • symptoms of infection 5 days prior to beginning of the study
  • comorbidity that could prevent patient from using Vitalograph®AIM to teach patient proper inhalation technique (i.e. advanced cognitive disorders, mental diseases, crucial neurological, vision or hearing disorders).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Adults with asthma or COPD
Assessment of inhalation technique by three methods in all patients
Assessment of inhalation technique by 3 methods in every patient

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of reliability of assessment of inhalation technique by checklist method in patients with asthma and COPD
Time Frame: baseline
Assessment of reliability of checklist method measured by 2 observers by kappa Cohen coefficient
baseline
Comparison of reliability of assessment of inhalation technique by 4 grade scale in patients with asthma and COPD
Time Frame: baseline
Assessment of reliability of 4 grade scale measured by 2 observers by kappa Cohen coefficient
baseline
Comparison of validity of assessment of inhalation technique by checklist method in patients with asthma and COPD
Time Frame: baseline
Assessment of validity of checklist method measured by convergence between observer and an expert baseline by kappa Cohen coefficient
baseline
Comparison of validity of assessment of inhalation technique by 4 grade scale in patients with asthma and COPD
Time Frame: baseline
Assessment of validity of 4 grade scale measured by convergence between observer and an expert baseline by kappa Cohen coefficient
baseline
Comparison of validity of assessment of inhalation technique by Vitalograph®AIM in patients with asthma and COPD
Time Frame: 30 minutes from baseline
Assessment of validity of Vitalograph®AIM method (convergence between assessment of Vitalograph®AIM and an expert)
30 minutes from baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Utility of Vitalograph® AIM in inhalation technique training
Time Frame: baseline and in 30 minutes
Difference in number of inhalation mistakes before and after Vitalograph® AIM based training
baseline and in 30 minutes
Comparison of repeatability of assessment of inhalation technique by checklist method in patients with asthma and COPD
Time Frame: baseline and in 30 minutes
Assessment of reliability of checklist method measured by 1 observer baseline and in 30 minutes by kappa Cohen coefficient
baseline and in 30 minutes
Comparison of repeatability of assessment of inhalation technique by 4 grade scale in patients with asthma and COPD
Time Frame: baseline and in 30 minutes
Assessment of reliability of 4 grade scale measured by 1 observer baseline and in 30 minutes by kappa Cohen coefficient
baseline and in 30 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 10, 2019

Primary Completion (Actual)

October 1, 2022

Study Completion (Actual)

December 30, 2022

Study Registration Dates

First Submitted

December 16, 2019

First Submitted That Met QC Criteria

April 14, 2020

First Posted (Actual)

April 16, 2020

Study Record Updates

Last Update Posted (Estimate)

February 21, 2023

Last Update Submitted That Met QC Criteria

February 19, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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