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A Patient-Centered Asthma Management Communication Intervention for Rural Latino Children

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ClinicalTrials.gov Identifier: NCT04633018
Recruitment Status : Recruiting
First Posted : November 17, 2020
Last Update Posted : September 29, 2021
Sponsor:
Information provided by (Responsible Party):
Robin Dawson, University of South Carolina

Brief Summary:
The purpose of this research is to develop and evaluate an mHealth communication intervention designed to improve asthma medication adherence amongst rural Latino children in South Carolina.

Condition or disease Intervention/treatment Phase
Asthma Device: AsthmaMD mobile application Other: Usual care Not Applicable

Detailed Description:

The overall prevalence of asthma is highest in the US south, which has one of the fastest growing Latino populations in the country. In South Carolina, asthma is the leading cause of children's hospitalization and emergency department (ED) visits, with significant direct and indirect costs. Although rates of childhood asthma are lower in Latinos (with the exception of children of Puerto Rican origin) than in whites, Latinos are more likely to have a higher incidence of uncontrolled asthma symptoms, ED visits, repeat hospitalizations, and poorer health in general. Current interventions addressing asthma control include outpatient clinic based and home visitation programs. Rural Latino families have difficulty participating with these types of programs due to work, family, and transportation constraints.

The adaptability of mobile apps holds the potential to target the unique challenges to management experienced by rural Latino children with asthma experience. The goal of this study is to develop and evaluate a patient-centered collaborative intervention between rural Latino children with asthma and their families, school-based nursing, and primary care providers, facilitated by the use of a smart phone based bilingual mobile app. The specific aims are to:

  1. Produce and validate a Spanish translation of an existing asthma management app and evaluate its usability with Latino parents of children with asthma; and
  2. Develop and evaluate a triadic, patient-centered asthma intervention preliminary protocol, facilitated by the bilingual mobile app validated in aim 1.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 30 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: A Patient-Centered Asthma Management Communication Intervention for Rural Latino
Actual Study Start Date : August 1, 2019
Estimated Primary Completion Date : December 30, 2021
Estimated Study Completion Date : August 1, 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Asthma

Arm Intervention/treatment
Experimental: Patient-centered asthma intervention feasibility
Investigate the effect of the patient-centered asthma intervention using the AsthmaMD app on school days missed and medication adherence.
Device: AsthmaMD mobile application
asthma management app with Spanish-language user interface

Experimental: Wait list control
Control group with usual care (not using app).
Other: Usual care
Asthma management without the app




Primary Outcome Measures :
  1. Mobile app usability and acceptability [ Time Frame: 1 week ]
    Participants with Spanish as first language use the translated app for ease of use and identification of interface problems

  2. Preliminary protocol testing of mobile app-facilitated triadic communication [ Time Frame: 3 months ]
    Develop and evaluate a triadic, patient-centered asthma intervention preliminary protocol, facilitated by the Spanish language mobile app. Post-intervention data regarding the experiences of the participants in this collaborative intervention will be obtained through a post-intervention focus group facilitated by the PI with the PCPs and school nurses, and five interviews conducted by a bilingual research assistant with the Latino families.

  3. Investigate the feasibility of the patient-centered asthma intervention [ Time Frame: 6 months ]
    Investigate the feasibility of the patient-centered asthma intervention from aim 2 using a wait list randomized control trial (RCT) to investigate the effects of the intervention on school days missed and medication adherence. Anticipated quantitative data includes the information entered into the app, encrypted, and transmitted to the school nurse by the parent/caregiver. These data will include selected NIH/AHRQ standardized asthma outcomes,47 including the primary outcome measures of medication adherence information (asthma medication ratio48 - predictive of childhood asthma ED visits and hospitalizations) and school days missed.


Secondary Outcome Measures :
  1. Medication adherence and lung function tests [ Time Frame: 6 months ]
    Secondary outcome measures include frequency of rescue inhaler use, as well as asthma exacerbations, outpatient clinic visits, and emergency department visits. Lung capacity will be obtained pre- and post-intervention/bronchodilation using spirometry49 to obtain relevant lung function variables such as FEV1 and FEV1/FVC. Measures from the control group will include medication counts, number of asthma exacerbations, ED/outpatient clinic visits, and spirometry measures on enrollment, during the intervention phase, and again at the end of the intervention.



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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

1) children self/family-identified as Hispanic or Latino, 2) school-aged (5-12 years) and attends school within the Lancaster County School District, 3) has received a diagnosis of asthma from a health care provider and is taking a controller medication, and 4) parents/primary caregiver (e.g., grandparents, extended family) language of preference is Spanish.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04633018


Contacts
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Contact: Robin Dawson (803) 576-6021 robin.dawson@sc.edu

Locations
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United States, South Carolina
Lancaster County School District Recruiting
Lancaster, South Carolina, United States, 29720
Contact: Leigh Lever, RN    803-416-8884    Leigh.Lever@lcsdmail.net   
Sponsors and Collaborators
University of South Carolina
Investigators
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Principal Investigator: Robin M Dawson, PhD University of South Carolina College of Nursing
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Robin Dawson, Associate Professor, University of South Carolina
ClinicalTrials.gov Identifier: NCT04633018    
Other Study ID Numbers: 1K23HL133596-01A1 ( U.S. NIH Grant/Contract )
First Posted: November 17, 2020    Key Record Dates
Last Update Posted: September 29, 2021
Last Verified: September 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: Yes
Product Manufactured in and Exported from the U.S.: No
Keywords provided by Robin Dawson, University of South Carolina:
mHealth
Latino
asthma
limited English proficiency
pediatrics
school nursing
Additional relevant MeSH terms:
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Asthma
Bronchial Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Lung Diseases
Respiratory Hypersensitivity
Hypersensitivity, Immediate
Hypersensitivity
Immune System Diseases