Skip to content

Effectiveness of Psychodermatologic Educational Modules on Atopic Dermatitis Patient Outcomes

Effectiveness of Psychodermatologic Educational Modules on Atopic Dermatitis Patient Outcomes

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07009483
Enrollment
42
Registered
2025-06-06
Start date
2025-06-02
Completion date
2026-12-31
Last updated
2025-08-27

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

Conditions

Atopic Dermatitis (AD)

Keywords

Atopic Dermatitis, Dermatology, Psychodermatology, Patient Education

Brief summary

In a previous part of this study, we created educational modules about the psychodermatology of inflammatory skin conditions, with a particular emphasis on atopic dermatitis, for patients. These modules will empower patients to better manage both the psychological and physical aspects of their skin conditions. As part of this project, we aim to conduct a clinical trial to determine the effectiveness of these modules on eczema severity and health-related quality of life in patients. We hope to use these findings to develop and disseminate accessible educational material on the psychological aspects of dermatologic care.

Interventions

BEHAVIORALPatient education modules providing information on the psychological aspects of atopic dermatitis treatment and management.

Provision of online patient educational modules (in addition to patients receiving regular clinical action/ appointments at the Kaye Edmonton Clinic, the Stollery Children's Hospital, and the Rao Dermatology Clinic for Atopic Dermatitis).

Sponsors

University of Alberta
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. New diagnosis or follow-up for previous diagnosis of Atopic Dermatitis. 2. Reliable internet access to be able to access the e-modules. 3. Able to speak English at a level required to understand the content of this study. 4. Child participants will be included in this study contingent on the consent of their guardian/caregiver(s). 5. Age range of eligible participants: Age 4 years and older.

Exclusion criteria

1. Does not have a new diagnosis or follow-up for previous diagnosis of Atopic Dermatitis. 2. Unable to access and/or navigate e-modules with reasonable support/instruction. 3. Unable to speak English at a level required to understand the content of this study. 4. Unable to provide informed consent. 5. Less than 4 years of age.

Design outcomes

Primary

MeasureTime frameDescription
Health-Related Quality of LifeBaseline, 4 weeks, and 12 weeksQuality of Life will be measured using the Dermatology Life Quality Index (DLQI). The scores range from 0 to 30 (higher score indicative of worse outcomes)

Secondary

MeasureTime frameDescription
Eczema Disease SeverityBaseline, 4 weeks, and 12 weeksEczema Disease Severity will be measures using the Patient-Oriented SCORing for Atopic Dermatitis (PO-SCORAD). Scores range between 0 and 103 points (higher score indicative of worse outcomes)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026