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Group Eczema Education Visits:Impact on Patient and Family Quality of Life

Oregon Health & Science University (OHSU) logo

Oregon Health & Science University (OHSU)

Status

Completed

Conditions

Eczema

Treatments

Other: Control group
Other: Group eczema education session

Study type

Interventional

Funder types

Other

Identifiers

NCT01143012
Group eczema education visits

Details and patient eligibility

About

The objective of this study is to determine whether group educational visits improve the quality of life of patients referred to the Dermatology Clinic. Secondary outcomes will be to determine whether group educational visits influences other key elements of patient care such as topical steroid usage, disease exacerbations, emergency visits, and phone calls to the office. Lastly, the investigators hope to evaluate which aspects of the educational visit were found to be the most helpful to families caring for children with atopic dermatitis (AD). Patients will be new atopic dermatitis referrals to OHSU dermatology and pediatric dermatology clinics. All consecutive patients with such appointments during a three month time period will be screened for participation in the study. Parents will be recruited via telephone. In the intervention group, parents will be invited to participate in a group education visit prior to their first appointment with a dermatologist. All parents in the study will fill out questionnaires. The children involved in the study will be assigned an eczema severity score during their routine visits, but this will be incorporated into the regular clinic assessment. The Childhood Atopic Dermatitis Impact Scale (CADIS) assesses the quality of life in households with children who have atopic dermatitis. The Eczema Area and Severity Index (EASI) measures the extent and severity of the patient's atopic dermatitis. The change in CADIS scores will be analyzed to determine if there is a more significant improvement in quality of life for the group in which parents receive the group eczema education visit.

Enrollment

36 patients

Sex

All

Ages

2 months to 6 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children ages 2 months though 6 years.
  • Participants must carry a diagnosis of atopic dermatitis according to the Hanifin and Rajka criteria.
  • New patients or consultations at an OHSU clinic.
  • English-speaking families will be included in this study

Exclusion criteria

  • Subjects who have been on systemic therapies for treatment of their atopic dermatitis (prednisone or cyclosporine)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

Group eczema education session
Active Comparator group
Description:
One group will attend a group eczema education session. All subjects will answer quality of life questions two times.
Treatment:
Other: Group eczema education session
Control group
Active Comparator group
Description:
The other group will not attend the group eczema education session. Both groups will be asked quality of life questions two times.
Treatment:
Other: Control group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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