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NCT Number: NCT06388460

Asthma Link Effectiveness Trial

The goal of this cluster Randomized Control Trial is to determine the effectiveness of Asthma Link, a school supervised asthma therapy program, compared with an educational asthma workbook, in improving asthma symptoms for children with poorly controlled asthma aged 5-14.

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Key information

Age range

5 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Massachusetts Chan Medical School

Worcester, Massachusetts, 01655, United States

Location status: Recruiting

Location contact

MIchelle Trivedi, MD MPH

PRINCIPAL_INVESTIGATOR

Michelle Spano

CONTACT

[email protected]

5088562990

About this study

Asthma is an extremely common chronic disease in childhood with significant morbidity. The majority of asthma morbidity in children is due to medication non-adherence, and both morbidity and medication non-adherence disproportionately impact minoritized children. School-supervised asthma therapy ensures that children receive their preventive asthma medication daily at school and has shown efficacy in improving medication adherence and asthma health outcomes, particularly in low-income and racial/ethnic minority children. However, this strategy has not been widely adopted in practice to produce meaningful public health impact. To address this gap, the study team developed a new model, Asthma Link, which partners pediatric practices, schools, and families to deliver school-supervised asthma therapy. This intervention leverages established infrastructure and requires minimal resources to operate, enhancing sustainability in a real-world setting. The pilot trial of Asthma Link showed improved asthma symptoms when compared to an enhanced usual care condition, particularly among low-income, Black and Latino children, and demonstrated trial feasibility. Moreover, the research team has rigorously adapted this intervention for real-world use using input from diverse, multi-level community stakeholders.

This 14 site cluster randomized controlled trial will determine the effectiveness of Asthma Link versus an enhanced usual care condition in improving asthma health outcomes in school-aged children with poorly controlled asthma.

The investigators central hypothesis is that children in Asthma Link will have higher Asthma Control Test scores at 6 months compared with children in enhanced usual care; with maintained improvements at 12 months. The secondary hypothesis is that children in Asthma Link will have higher inhaled corticosteroid adherence and quality of life scores, and lower rates of asthma exacerbations, school absences and parental lost workdays compared with children in the enhanced usual care condition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

STUDY INCLUSION/EXCLUSION CRITERIA:

Child Inclusion Criteria:

  • Meet the eligibility criteria for Asthma Link (as described below)
  • Enrolled in Asthma Link (if randomized to the Asthma Link Condition)
  • Able and willing to provide informed assent

Child Exclusion Criteria:

  • Unable or unwilling to provide informed assent
  • Developmental delay that would prevent study participation.

Parent Inclusion Criteria:

  • Parent/guardian to patient
  • 18 years or older
  • Able to understand and communicate in English or Spanish
  • Able and willing to provide informed consent.

Child eligibility for children enrolled in Asthma Link:

  • children aged 5-14 years (enrolled in grade K-8)
  • prescribed daily inhaled corticosteroid (ICS) for asthma
  • Asthma Control Test (ACT) score ≤19 OR 1 or more of ANY of following in the past 1 year: course of oral steroids, hospitalization, Emergency Department visit, sick visit for asthma
  • parent/child report of poor ICS adherence on adherence checklist- i.e. child or parent says "Yes" when provider asks if they have difficulty remembering to take their medication or if they regularly take medication holidays or breaks
  • able and willing to assent
  • parental permission
  • English or Spanish speaking

Treatment and study plan

Asthma Link

Other

Providers enroll patients to receive school-supervised asthma therapy and an asthma educational workbook

Enhanced usual care

Other

Providers enroll patients to receive an asthma educational workbook

Primary outcomes

  1. Improving Asthma Symptoms

    Time frame: Baseline, 6 months, 12 months

    Asthma Control Test to measure child's asthma control on a scale of 0-25. A score of 19 or less is considered poorly controlled asthma.

Secondary outcomes

  1. Improving Medication Adherence

    Time frame: Baseline, 6 months, 12 months

    Survey to measure medication adherence

  2. Improving Healthcare Utilization

    Time frame: Baseline, 6 months, 12 months

    Survey questions to measure # of emergency room visits, # of hospital admissions, # of oral steroid courses due to asthma

  3. Reducing Parental Lost Workdays

    Time frame: Baseline, 6 months, 12 months

    Survey to measure the number of days a parent has missed work

  4. Reducing School Absences

    Time frame: Baseline, 6 months, 12 months

    Survey to measure the number of days a child has missed school

  5. Improving Quality of Life

    Time frame: Baseline, 6 months, 12 months

    Survey to measure the quality of life of the child and parent

Study contacts

Contact information is provided by the study sponsor or research team.

Michelle Spano, MA

CONTACT

[email protected]

17746966875

Michelle Trivedi, MD

CONTACT

[email protected]

7744418086

Sponsors and collaborators

Lead sponsor

University of Massachusetts, Worcester

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • National Institutes of Health (NIH)

Registry information

Official study title

Asthma Link: A Partnership Between Pediatric Practices, Schools, and Families to Improve Medication Adherence and Health Outcomes in Children With Poorly Controlled Asthma

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Apr 29, 2024
Registry last updated
May 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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