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Pictograms to Facilitate Comprehension of Medical Indications (SIMAP)

Primary Purpose

Asthma Chronic, Adherence, Medication, Primary Health Care

Status
Recruiting
Phase
Not Applicable
Locations
Chile
Study Type
Interventional
Intervention
SIMAP
Usual Care
Sponsored by
Universidad de Concepcion
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Asthma Chronic focused on measuring Asthma Chronic, Adherence, Medication, Primary Health Care

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Adult patients aged 18 to 65 years with a recent diagnosis of bronchial asthma (<=15 days) based on 2018 Global Initiative For Asthma (GINA) criteria. Diagnosis substantiated clinically and with consistent spirometry results as established by current GINA guidelines. Patients who are to initiate bronchodilator treatment, including at least one inhaled corticosteroid and one short-acting bronchodilator. Exclusion Criteria: Patients presenting obstructive bronchial pathology other than bronchial asthma (chronic obstructive pulmonary disease, mixed states, etc.), Patients who have participated in the pictogram design phase (Stage 1 of the project), Patients with a diagnosis of dementia, diagnosis of harmful use of alcohol and other drugs according to the International Classification of Diseases (ICD-10). Patients with significant ophthalmologic pathology that prevents the use of pictograms. Patients who do not wish to participate in the project.

Sites / Locations

  • Dirección de Administración de Hualpen
  • Dirección de Administración Salud de Talcahuano
  • Ilustre Municipalidad de San Antonio
  • Corporación Municipal de ValparaisoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Pictogram Group

Usual Care Group

Arm Description

This intervention consists of using a pictogram system called SIMAP which was developed and validated in previous research. Participants allocated to this arm will received a pictographic depiction of their medical indications generated by an automated system. Information will include a description of inhaler functions, inhaler technique and correct aerochamber use.

These patients will receive their medical indications in the usual way, as established by the health team of the participating clinics. In addition, these patients will receive a bronchial asthma information leaflet as part of the usual education when explaining the disease. No pictograms will be included in these leaflets.

Outcomes

Primary Outcome Measures

Disease Control at 60 days
60 days after randomisation between groups using the Asthma Control Test.
Disease Control at 30 days
Asthma control achieved at 30 days after randomisation between groups using the Asthma Control Test.
Disease Control at 7 days
Asthma control achieved at 7 days after randomisation between groups using the Asthma Control Test.

Secondary Outcome Measures

Inhaler technique
Proportion of participants displaying a correct inhaler technique between groups.
Aerochamber use
Proportion of participants using an aerochamber between groups

Full Information

First Posted
September 6, 2022
Last Updated
December 6, 2022
Sponsor
Universidad de Concepcion
Collaborators
Universidad de Valparaiso, Comisión Nacional de Investigación Científica y Tecnológica, Servicio de Salud Talcahuano, ILUSTRE MUNICIPALIDAD DE HUALPEN, Dirección de Administración de Salud Municipal de Talcahuano
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1. Study Identification

Unique Protocol Identification Number
NCT05609760
Brief Title
Pictograms to Facilitate Comprehension of Medical Indications
Acronym
SIMAP
Official Title
Effects of an Automated System of Pictograms to Facilitate Comprehension of Medical Indications: A Randomised Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2022 (Actual)
Primary Completion Date
February 1, 2023 (Anticipated)
Study Completion Date
April 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universidad de Concepcion
Collaborators
Universidad de Valparaiso, Comisión Nacional de Investigación Científica y Tecnológica, Servicio de Salud Talcahuano, ILUSTRE MUNICIPALIDAD DE HUALPEN, Dirección de Administración de Salud Municipal de Talcahuano

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
SIMAP is a triple-masked randomised trial aimed at assessing whether an automated system of pictograms associated to medical indications results in better comprehension and adherence of said indications. Adult patients with a recent diagnosis of asthma will be randomised to receive a pictographic depiction of their treatments and recommended interventions or standard communication without assistance from their attending physician. Patients will be followed-up for 60 days using the Asthma Control Questionnaire (ACT). The primary endpoint of this study is the degree of asthma control as assessed by the aforementioned questionnaire. Secondary outcomes include the number of hospitalisations, emergency care unit visits and the need to increase bronchodilator therapy as per current Global Initiative for Asthma guidelines. Outcomes will be analysed under the intention-to-treat principle by a statistician unaware of treatment allocation.
Detailed Description
In this triple-masked randomised trial, adult participants with a recent diagnosis of asthma (<15 days) will be allocated to receive a pictographic depiction of their medical indications or a standard description of said indications. Eligible patients will include those between 18 and 65 years of age with a diagnosis of asthma established by standard clinical recommendations (clinical and spirometric criteria as established by Global Initiative for Asthma - GINA - guidelines) and in whom therapy including a bronchodilator and a controller medication (typically an inhaled steroid) is planned to be initiated. Patients with another cause of bronchial obstruction (such as COPD), those with cognitive or visual impairments that hampers the understanding of pictograms or those with a history of alcoholism or alcohol abuse will be excluded. Patients will be randomised using a permuted block sequence which shall be kept hidden from other investigators. Participants will be followed-up at seven, thirty and sixty-day intervals using the Asthma Control Questionnaire (ACT), which is the primary outcome of this study. Participants, clinical evaluators, analysts and sponsors will be kept unaware of treatment allocation. Secondary endpoints include the inhaler technique, the correct depiction of inhaler medication purpose, the rate of emergency care visits between groups, the rate of hospitalisations between groups and the need to increase bronchodilator therapy during scheduled visits within the trial. All analyses will be conducted using the intention-to-treat principle.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma Chronic, Adherence, Medication, Primary Health Care
Keywords
Asthma Chronic, Adherence, Medication, Primary Health Care

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized clinical trial of parallel groups with triple masking amongst patients with a recent diagnosis of asthma (<=15 days) in primary care.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Participants, clinical investigators, outcome assessors, analysts and sponsors will be kept unaware of treatment allocation. The masking of the participating patients will be carried out through an informative brochure on bronchial asthma delivered as part of the usual education, albeit without using pictograms.
Allocation
Randomized
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pictogram Group
Arm Type
Experimental
Arm Description
This intervention consists of using a pictogram system called SIMAP which was developed and validated in previous research. Participants allocated to this arm will received a pictographic depiction of their medical indications generated by an automated system. Information will include a description of inhaler functions, inhaler technique and correct aerochamber use.
Arm Title
Usual Care Group
Arm Type
Sham Comparator
Arm Description
These patients will receive their medical indications in the usual way, as established by the health team of the participating clinics. In addition, these patients will receive a bronchial asthma information leaflet as part of the usual education when explaining the disease. No pictograms will be included in these leaflets.
Intervention Type
Other
Intervention Name(s)
SIMAP
Intervention Description
Pictographic depiction of medical indications alongside standard communication of these recommendations.
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Standard communication by medical staff of treatment indications for asthma. An informative leaflet will be delivered as well.
Primary Outcome Measure Information:
Title
Disease Control at 60 days
Description
60 days after randomisation between groups using the Asthma Control Test.
Time Frame
60 days
Title
Disease Control at 30 days
Description
Asthma control achieved at 30 days after randomisation between groups using the Asthma Control Test.
Time Frame
30 days
Title
Disease Control at 7 days
Description
Asthma control achieved at 7 days after randomisation between groups using the Asthma Control Test.
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Inhaler technique
Description
Proportion of participants displaying a correct inhaler technique between groups.
Time Frame
60 days
Title
Aerochamber use
Description
Proportion of participants using an aerochamber between groups
Time Frame
60 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients aged 18 to 65 years with a recent diagnosis of bronchial asthma (<=15 days) based on 2018 Global Initiative For Asthma (GINA) criteria. Diagnosis substantiated clinically and with consistent spirometry results as established by current GINA guidelines. Patients who are to initiate bronchodilator treatment, including at least one inhaled corticosteroid and one short-acting bronchodilator. Exclusion Criteria: Patients presenting obstructive bronchial pathology other than bronchial asthma (chronic obstructive pulmonary disease, mixed states, etc.), Patients who have participated in the pictogram design phase (Stage 1 of the project), Patients with a diagnosis of dementia, diagnosis of harmful use of alcohol and other drugs according to the International Classification of Diseases (ICD-10). Patients with significant ophthalmologic pathology that prevents the use of pictograms. Patients who do not wish to participate in the project.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rosa L Figueroa, ScD
Phone
+56 9 924956932
Email
rosa.figueroa@biomedica.udec.cl
First Name & Middle Initial & Last Name or Official Title & Degree
María A Rodriguez, PhD
Phone
+56 41 2204302
Email
secrevrid@udec.cl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rosa L Figueroa, PhD
Organizational Affiliation
Universidad de Concepcion
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Carla Taramasco, PhD
Organizational Affiliation
Universidad de Valparaiso
Official's Role
Study Director
Facility Information:
Facility Name
Dirección de Administración de Hualpen
City
Hualpen
State/Province
Biobio
Country
Chile
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
OMAR GALVEZ, EU
Email
erahualpencillo@gmail.com
First Name & Middle Initial & Last Name & Degree
ALEJANDRA BOBADILLA
Email
alejandra.bobadillac@gmail.com
Facility Name
Dirección de Administración Salud de Talcahuano
City
Talcahuano
State/Province
Biobio
Country
Chile
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrea Grandon, klga
Email
agrandon.cesfamalp@gmail.com
First Name & Middle Initial & Last Name & Degree
Javier Vera, EU
Email
jvera.cesfamalp@gmail.com
Facility Name
Ilustre Municipalidad de San Antonio
City
San Antonio
State/Province
Valparaiso
Country
Chile
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria J Escobar
Email
mariajosescobar@gmail.com
Facility Name
Corporación Municipal de Valparaiso
City
Valparaíso
Country
Chile
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francisco Tapia
Email
ftapia@cmvalparaiso.cl
First Name & Middle Initial & Last Name & Degree
Renzo Vergara
Email
rvergara@cmvalparaiso.cl,

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34658302
Citation
Reddel HK, Bacharier LB, Bateman ED, Brightling CE, Brusselle GG, Buhl R, Cruz AA, Duijts L, Drazen JM, FitzGerald JM, Fleming LJ, Inoue H, Ko FW, Krishnan JA, Levy ML, Lin J, Mortimer K, Pitrez PM, Sheikh A, Yorgancioglu AA, Boulet LP. Global Initiative for Asthma Strategy 2021: Executive Summary and Rationale for Key Changes. Am J Respir Crit Care Med. 2022 Jan 1;205(1):17-35. doi: 10.1164/rccm.202109-2205PP.
Results Reference
background
PubMed Identifier
14713908
Citation
Nathan RA, Sorkness CA, Kosinski M, Schatz M, Li JT, Marcus P, Murray JJ, Pendergraft TB. Development of the asthma control test: a survey for assessing asthma control. J Allergy Clin Immunol. 2004 Jan;113(1):59-65. doi: 10.1016/j.jaci.2003.09.008.
Results Reference
background
PubMed Identifier
25555366
Citation
Perez-Yarza EG, Castro-Rodriguez JA, Villa Asensi JR, Garde Garde J, Hidalgo Bermejo FJ; Grupo VESCASI. [Validation of a Spanish version of the Childhood Asthma Control Test (Sc-ACT) for use in Spain]. An Pediatr (Barc). 2015 Aug;83(2):94-103. doi: 10.1016/j.anpedi.2014.10.031. Epub 2014 Dec 30. Spanish.
Results Reference
background
Citation
Alvear G, Figueroa L, Hurtado G, Moyano L. Evaluación del grado de control del asma en un centro de atención primaria. Un estudio descriptivo. Rev. chil. enferm. respir. 2016; 32 (2): 68-76. Spanish.
Results Reference
background
PubMed Identifier
25378914
Citation
Barros IM, Alcantara TS, Mesquita AR, Bispo ML, Rocha CE, Moreira VP, Lyra Junior DP. Understanding of pictograms from the United States Pharmacopeia Dispensing Information (USP-DI) among elderly Brazilians. Patient Prefer Adherence. 2014 Oct 29;8:1493-501. doi: 10.2147/PPA.S65301. eCollection 2014.
Results Reference
background
Links:
URL
http://www.bibliotecaminsal.cl/wp/wp-content/uploads/2016/04/Asma-Bronquial-Adultos.pdf
Description
Chilean Guide for Asthma Treatment

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Pictograms to Facilitate Comprehension of Medical Indications

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