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Communication tools for parents of children presenting to the Emergency Department with croup

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN39642997
Enrollment
420
Registered
2007-10-16
Start date
2007-10-15
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Acute obstructive laryngitis (croup) Respiratory Acute obstructive laryngitis

Interventions

Patients are randomly assigned to one of the following: 1. Experimental intervention is three booklets that integrate stories, as told by parents of children with croup attending the ED, with evidence

Sponsors

University of Alberta (Canada) - Department of Paediatrics
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Parents of children with a clinical diagnosis of croup 2. Parents must also meet the following criteria: 2.1. Have a telephone and be willing to be contacted for follow-up interviews 2.2. Fluent in English 2.3. Provide informed consent 2.4. No prior visit to an ED during this episode of the disease 2.5. No prior visit to an ED for another episode of croup during the study period

Exclusion criteria

Exclusion criteria: Parents will be excluded if: 1. Stridor is due to another cause (e.g., bacterial tracheitis, presence of a supraglottic foreign body) 2. Parent has previously been included in the study

Design outcomes

Primary

MeasureTime frame
Parental anxiety measured using the State-Trait Anxiety Inventory (STAI-S, Form Y). Anxiety will be measured at baseline, discharge from ED, one day post-discharge, and when child is symptom free.

Secondary

MeasureTime frame
1. Event impact 2. Parental knowledge, measured at day 3 post-discharge, 1 year post-discharge 3. Parental satisfaction with ED visit, measured at day 1 post-discharge 4. Decisional regret, measured at day 1 post-discharge 5. Incidence of return for medical care, measured at day 1, day 3 and every two days thereafter until child is symptom-free or until day 9 post-discharge 6. Healthcare utilisation patterns, measured at day 1, day 3 and every two days thereafter until child is symptom-free or until day 9 post-discharge, 1 year post-discharge 7. Costs, measured at day 1, day 3 and every two days thereafter until child is symptom-free or until day 9 post-discharge, 1 year post-discharge

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 10, 2026