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Telemedicine-Based Education for Asthma Control in Children

Effectiveness of Telemedicine-Based Education for Caregivers on Asthma Control in Children with Uncontrolled Asthma: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240529008
Enrollment
76
Registered
2024-05-29
Start date
2024-06-28
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Pediatric patients with uncontrolled asthma Telemedicine-Based Education Asthma Pediatrics Telemedicine Uncontrolled asthma

Interventions

Caregivers in the intervention group will receive a video call from the intervention researcher within 15 minutes. The call will include education on avoiding factors related to uncontrolled asthma, r
s practical steps at any time during the conversation. Additionally, questions about asthma management will be discussed, and tailored advice will be provided according to each child&#039
s condition.,The caregivers will receive a video call from the intervention researcher shortly for a health check and a reminder to follow the scheduled appointments.
Experimental Other,Sham Comparator Other
Telemedicine,Standard care

Sponsors

Thang Hoang Le
Lead Sponsor
Ly Cong Tran,Nghia Quang Bui
Collaborator

Eligibility

Sex/Gender
All
Age
4 Years to 16 Years

Inclusion criteria

Inclusion criteria: Pediatric asthma patients diagnosed according to the GINA guidelines, classified as having uncontrolled asthma, are managed and followed up for at least 1 month at the pediatric asthma unit of the outpatient department.

Exclusion criteria

Exclusion criteria: 1. Pediatric patients who do not cooperate or are unable to complete the Childhood Asthma Control Test questionnaire. 2. Caregivers who cannot complete the questionnaires related to the assessment of asthma control and associated factors. 3. Pediatric patients who have siblings participating in the study. 4. Patients currently participating in another clinical study (excluding non-interventional studies or registries). 5. Failure to return for a second visit within 6 months following enrollment.

Design outcomes

Primary

MeasureTime frame
The improvement of asthma control At second follow-up visit (ranging from 4 to 24 weeks after enrollment) Asthma Control Test/Childhood Asthma Control Test

Secondary

MeasureTime frame
The improvement of caregiver's knowledge regarding asthma control At second follow-up visit (ranging from 4 to 24 weeks after enrollment) Questionnaire,The improvement of caregiver's attitudes toward asthma management At second follow-up visit (ranging from 4 to 24 weeks after enrollment) A set of questions,The improvement of proper inhaler technique usage At second follow-up visit (ranging from 4 to 24 weeks after enrollment) Checklist

Countries

Vietnam

Contacts

Public ContactNghia Bui

Can Tho University of Medicine and Pharmacy

bqnghia@ctump.edu.vn0918398788

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026