Skip to content

Evaluation of an education method on the severity of the Atopic Dermatitis disease and on the quality of life of children and their guardians

Evaluation of an educational intervention on the severity of the disease Atopic Dermatitis and the quality of life of children and their caregivers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3m97hhq
Enrollment
Unknown
Registered
2023-09-11
Start date
2021-06-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Atopic dermatitis

Interventions

Participants were allocated into the control group and study group through simple randomization using the Randomizer platform. Single-blind, randomized, controlled clinical trial (researcher blind) St

Sponsors

Complexo Hospital de Clínicas da Universidade Federal do Paraná
Lead Sponsor
Complexo Hospital de Clínicas da Universidade Federal do Paraná
Collaborator

Eligibility

Age
No minimum to 15 Years

Inclusion criteria

Inclusion criteria: Children under the age of 15 and their respective primary caregiver who attend the consultation at the Pediatric Dermatology service of the Hospital de Clínicas Complex; children who meet the Hanifin and Rajka criteria for the clinical diagnosis of atopic dermatitis; children who do not have other chronic diseases, with the exception of mild asthma and rhinitis; children accompanied by their primary caregivers; literate caregivers who answer the Quality of Life questionnaires; guardians who have a cell phone that supports the Whatsapp® application and have enabled the read confirmation option and who have an active phone line and mobile Internet or WiFi available; who agree to participate and sign the Informed Consent Form and Informed Consent Form, when applicable

Exclusion criteria

Exclusion criteria: They started using immunosuppressants during the evaluation period or up to 2 months before inclusion in the study; who do not return for revaluations in the specified period; withdraw the Free and Informed Consent form and the Free and Informed Consent Term

Design outcomes

Primary

MeasureTime frame
Decrease in the severity of atopic dermatitis, through the receipt of text messages with information about the disease, based on the finding of a significantly statistical decrease in the severity scores of atopic dermatitis

Secondary

MeasureTime frame
Improvement in the quality of life of participants with atopic dermatitis, through the receipt of text messages with information about the disease, based on the observation of a significantly statistical increase in the scores in the quality of life questionnaires in atopic dermatitis.

Countries

Brazil

Contacts

Public ContactRenata Imoto

Complexo Hospital de Clínicas da Universidade Federal do Paraná

natarobl@hotmail.com+55(41)33601041

Outcome results

None listed

Source: REBEC (via WHO ICTRP)