University of Massachusetts
Worcester, Massachusetts, 01655, United States
NCT Number: NCT04942379
The goal of this study is to assess the feasibility of a clinical trial to evaluate the impact and process of deploying school-supervised asthma therapy in a real-world setting for children with poorly controlled asthma (aged 6-17 years).
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Notify Me6 year–17 year
All sexes
Interventional
Not applicable
Worcester, Massachusetts, 01655, United States
The proposed 4-site pilot cluster randomized controlled trial will assess the feasibility of conducting a clinical trial of Asthma Link, a real-world school-supervised asthma therapy program. We will compare the impact of Asthma Link deployed in 2 pediatric practice sites versus Enhanced usual care deployed in 2 comparator sites, with 18 parent-child dyads enrolled per site (N=72 dyads).
Primary trial outcomes will be participant recruitment, retention, and intervention fidelity. Secondary trial outcomes will be differences in the frequency of asthma symptoms, emergency department visits, hospital admissions, courses of oral corticosteroids, spirometry values, medication adherence and school absences between intervention and enhanced usual care sites at 3, 6 and 12 month follow up. Additionally we will assess process outcomes (acceptability, adoption, costs, sustainability).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
STUDY INCLUSION/EXCLUSION CRITERIA:
Child Inclusion Criteria:
Child Exclusion Criteria:
Parent Inclusion Criteria:
Parent Exclusion Criteria:
Medical Provider, School Nurse, Asthma Champion Inclusion Criteria:
Medical Provider, School Nurse, Asthma Champion Exclusion Criteria:
Child eligibility for children enrolled in Asthma Link:
Providers enroll patients in school nurse supervised daily controller asthma medication delivery
Providers counsel patients on behavioral strategies to improve medication adherence. Patients also receive an asthma workbook outlining behavioral strategies for asthma medication adherence.
Time frame: Baseline
Research staff will track number of patients screened during enrollment process.
Time frame: Baseline
Research staff will track number of eligible participants who meeting study criteria during the enrollment process.
Time frame: Baseline
Research staff will track number of patients recruited into the study after they are assessed for eligibility.
Time frame: Baseline
Research staff will track the number of patients that were not enrolled or refused to participate in the study along with the reasons for non-enrollment.
Time frame: Up to end of study, approximately 12 months
Research staff to track number of participants who drop out of the study and note reasons for not completing study.
Time frame: Up to end of study, approximately 12 months
Research staff to track number of participants lost to follow-up, who did not complete the 12 month study assessment.
Time frame: Baseline
Research staff to assess for intervention fidelity within the pediatric practice through a checklist for pediatric staff to assess percentage of eligible children enrolled.
Time frame: Up to end of study, approximately 12 months
Research staff to assess for intervention fidelity by school nurse report of percentage of enrolled students receiving supervised therapy.
Time frame: Up to end of study, approximately 12 months
Research staff to assess for intervention fidelity by school nurse checklist of each enrolled child attending daily school nurse sessions and his/her family bringing medication to school.
Time frame: 3 months, 6 months, 12 months
Research staff will assess acceptability of the study among stakeholders (parent-child dyads, medical providers, school nurses) via a survey in which we will ask stakeholders to rate each component of the Asthma Link intervention using a study specific Acceptability scale ranging from 1 (strongly disagree) to 5 (strongly agree). Qualitative interviews will be performed with stakeholders at 12 months
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess adoption of the intervention via Pediatric practice log to track number of providers offering Asthma Link.
Time frame: 3 months, 6 months, 12 months
Research staff will assess adoption of the intervention via survey to family at each survey timepoint of study to assess ability to obtain 2 inhalers (one for home and one for school) and deliver medicine to school.
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess adoption of the intervention via school nurse log to track family bringing in medicine to school and frequency of child coming to nurses office to receive the medication.
Time frame: School nurses and pediatric practices 6 and 12 months/Parents 3, 6 and 12 months
Research staff will use survey questions to assess time and costs for school nurses to review the toolkit and administer the intervention, pediatric providers to implement the program, and parents to participate in the intervention
Time frame: 3 months, 6 months, 12 months
Research staff will use a survey questions to parents, pediatric practice staff and school staff
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess asthma symptoms utilizing spirometry to measure Forced Expiratory Volume.
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess asthma symptoms utilizing the validated measure: Asthma Control Test (ACT) which consists of parent's assessment of level of control over child's asthma symptoms in the previous 4 weeks.
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess asthma symptoms utilizing the validated measure: Maximum Symptom Days (the largest value of the number of days in the previous 2 weeks that a parent reports that their child experienced a) cough, wheezing, or shortness of breath, b) slowed activities due to symptoms, or 3)nocturnal awakening due to these symptoms.
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess the frequency of healthcare utilization (# of emergency room visits, # of hospital admissions, # of oral steroid courses, and # of urgent care visits) due to asthma through parent report on surveys and medical record review.
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess medication adherence via a survey questions administered to parents and through pharmacy refill data.
Time frame: Baseline, 3 months, 6 months, 12 months
Research staff will assess school absences via parent report and school nurse report
University of Massachusetts, Worcester
Other
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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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