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Brief Cognitive Behavioral Therapy to Treat Itch Rumination Itch CBT in Eczema

Brief Cognitive Behavioral Therapy to Treat Itch Rumination Itch CBT in Eczema

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04486742
Enrollment
20
Registered
2020-07-27
Start date
2020-09-01
Completion date
2021-12-21
Last updated
2023-11-09

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

Conditions

Atopic Dermatitis

Keywords

Pediatric

Brief summary

The main purpose of this study is to adapt cognitive behavior therapy (CBT) to improve itch in children with eczema.

Detailed description

Eczema is characterized by chronic itch. Many children develop a chronic focus (rumination) on their itch. Rumination is a maladaptive method of responding to distress, in which the individual thinks obsessively about the source of distress. The rumination on chronic itch in eczema can have detrimental effects on one's quality of life, as well as induce significant anxiety about when itch will return, how long it will last, and how it will affect physical and social functioning. Cognitive behavior therapy (CBT) is a frontline treatment for rumination, as it focuses on teaching strategies so that the individual can examine distressing thoughts objectively and determine their validity, replace negative thinking patterns with more adaptive thought patterns, and increase the individual's awareness to their problematic thought patterns. Additionally, CBT helps the individual to implement behavioral strategies to cope with possibly anxiety-inducing situations, such as scratching while trying to go to sleep. The investigators hypothesize that an Itch CBT intervention is an effective, non-medication-based, easy to implement strategy to improve itch in children with eczema.

Interventions

BEHAVIORALItch CBT

Telemedicine CBT sessions with a therapist to address atopic dermatitis related concerns.

Sponsors

Ann & Robert H Lurie Children's Hospital of Chicago
CollaboratorOTHER
Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Moderate to severe atopic dermatitis \[assessed by Patient Oriented Eczema Measure (POEM)score of \>-8 OR NRS itch score of \>= 4\]. * English speaking. * Currently receiving treatment at Lurie Children's Hospital for atopic dermatitis. * Parent or guardian available to participate in protocol. * Have sufficient technology (e.g., cell phone, computer, tablet, etc.) that can be used to access Zoom conference technology for telemedicine visits.

Exclusion criteria

* Inability to comprehend and complete questionnaires. * History of intellectual disability or psychosis.

Design outcomes

Primary

MeasureTime frameDescription
Itch Severity Numerical Rating ScaleBaseline to Week 4Numerical rating scale to assess itch severity, scale of 0-10, higher score means higher itch severity and worse outcome.

Secondary

MeasureTime frameDescription
Itch Rumination QuestionnaireBaseline to Week 4Questionnaire to assess common fear and anxiety around itch
PROMIS Anxiety and DepressionBaseline to Week 4Questionnaire to assess anxiety and depression symptoms in pediatric populations
PROMIS Pediatric Itch - Short Form 1 (2+6)Baseline to Week 4Questionnaire to assess level and severity of itch and common disturbances due to itch (social, emotional, physical)

Countries

United States

Outcome results

None listed

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