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Talking Card for Asthma

The Talking Card for Asthma: A Recordable Audio Discharge Instruction Device to Improve Asthma Control

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02041013
Enrollment
64
Registered
2014-01-20
Start date
2009-11-30
Completion date
2012-10-31
Last updated
2015-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Asthma, Health Literacy

Brief summary

The research goal is to explore the use and effects of a custom-recordable audio discharge instruction card (Talking Card) in the pediatric health care setting. This study will address a primary, experimental research question: can pediatric asthma control be improved through the distribution of a custom-recorded audio asthma instruction card to parents at the health provider's office? Secondary, descriptive objectives will be to evaluate feasibility of Talking Card delivery and to collect and summarize parental reactions to the design and use of the audio discharge instruction card. The specific aims of this study are: 1. To compare the change in mean Childhood Asthma Control Test (C-ACT) scores for children aged 4 through 11 years with uncontrolled asthma receiving a custom-recorded asthma instruction card to the change in mean C-ACT scores for those receiving usual care. 2. To measure the use and impressions of a custom-recordable audio asthma discharge instruction card among primary caregivers of children with uncontrolled asthma through quantitative and qualitative survey questions. The investigators hypothesize that: 1\) Asthma control in children 4 through 11 years of age with uncontrolled asthma, as measured by the C-ACT, will improve to a greater extent among those receiving a custom-recordable audio discharge instruction card than among those receiving usual care.

Interventions

OTHERTaking Card

Recordable greeting card-style discharge instruction card

Sponsors

University of South Florida
CollaboratorOTHER
Children's Mercy Hospital Kansas City
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 11 Years
Healthy volunteers
No

Inclusion criteria

* Child age 4 through 11 years old * English-speaking primary caregiver * Enrollment in Medicaid insurance company within 12 months of study recruitment (original Kansas City site criterion, removed on revision) * Diagnosis of asthma (ICD-9 code 493.0) within 12 months of study recruitment * Visit to study site clinic for asthma within 12 months of study recruitment

Exclusion criteria

* History of premature birth less than 33 weeks gestation or requirement of a significant level of respiratory care including mechanical ventilation as a neonate * Any major chronic illness including but not limited to non-skin cancer, cystic fibrosis, bronchiectasis, sickle cell anemia, endocrine disease, congenital heart disease, congestive heart failure, stroke, severe hypertension, insulin-dependent diabetes mellitus, renal failure, liver disorders, immunodeficiency states, significant neuro-developmental delay or behavioral disorders (excluding mild attention deficit hyperactivity disorder), or other conditions that would interfere with participation in the study * Visit to any primary care provider giving asthma action plan advice during the previous month * Anticipated departure from study area before study period ends (3-month follow-up)

Design outcomes

Primary

MeasureTime frameDescription
Asthma Control (C-ACT)3 monthsChildhood Asthma Control Test (C-ACT) score, measured repeatedly across 3 visits

Secondary

MeasureTime frameDescription
Parental Card Use and Satisfaction3 monthsSurvey of parental card use and satisfaction with card performance, measured repeatedly across 3 visits

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026