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Internet-based Mindfulness and Exposure Treatment for Atopic Dermatitis

Primary Purpose

Atopic Dermatitis

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Internet mindfulness&exposure treatment
Treatment as usual
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atopic Dermatitis

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Fulfills the diagnostic criteria for atopic dermatitis in accordance with Williams criteria 1994
  • at the time of inclusion the eczema should be at least moderate according to The Patient Oriented Eczema Measure (POEM)
  • Regular access to computer and internet connection
  • If on antidepressant or regular sleep medication, the medication should be stable for at least one month prior to inclusion and the person should be willing to keep the medication stable throughout the study
  • possibility to actively carry out the treatment (not go for longer journeys, do homework)
  • good understanding of written and spoken Swedish

Exclusion Criteria:

  • severe psychiatric illness (bipolar disorder, schizophrenia or other psychotic illness, substance, alcohol abuse, severe depression, suicide risk)
  • difficulties with reading or writing
  • ongoing treatment for cancer
  • pregnancy
  • other psychological treatment that i ongoing or recently terminated
  • stronger anxiety-reducing medication such as benzodiazepines
  • treatment with antibiotics that is ongoing or has been terminated less than one month prior to inclusion
  • Psoriasis
  • UV-light treatment that is ongoing or has been terminated less than one month prior to inclusion
  • oral treatment for eczema that is ongoing or has been terminated less than two month prior to inclusion

Sites / Locations

  • Karolinska Institutet

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Internet mindfulness&exposure treatment

Treatment as usual

Arm Description

A 12-week treatment where the main treatment components are mindfulness, exposure and response prevention, a form of cognitive behavior therapy. The treatment entails methods to increase acceptance and non-reactivity to aversive thoughts and emotions associated with AD. The treatment is delivered via the Internet and comprises 10 modules, each with a specific theme. Throughout treatment, the patient is given structured exercises to work with on a daily basis.

Participants receive information about moisturizer and anti-inflammatory lotion treatment which is treatment as usual. After 12 weeks, patients in this arm are crossed over to treatment.

Outcomes

Primary Outcome Measures

Patient-Oriented Eczema Measure (POEM)
Change in POEM at post-treatment and 6 and 12 month follow-ups compared to baseline

Secondary Outcome Measures

Visual analogue scale itch (VAS-itch)
Change in VAS-scratch at post-treatment and 6 and 12 month follow-ups compared to baseline
Visual analogue scale scratch (VAS-scratch)
Change in VAS-scratch at post-treatment and 6 and 12 month follow-ups compared to baseline
Visual analogue scale sleep (VAS-sleep)
Change in VAS-sleep at post-treatment and 6 and 12 month follow-ups compared to baseline
Dermatology Quality of Life Index (DLQI)
Change in DLQI at post-treatment and 6 and 12 month follow-ups compared to baseline
Beck Anxiety Inventory (BAI)
Change in BAI at post-treatment and 6 and 12 month follow-ups compared to baseline
Patient Health Questionnaire-9 (PHQ-9)
Change in PHQ-9 at post-treatment and 6 and 12 month follow-ups compared to baseline
Perceived stress scale (PSS)
Change in PSS at post-treatment and 6 and 12 month follow-ups compared to baseline
5-dimensions itch scale (5-D itch scale)
Change in 5-D itch scale at post-treatment and 6 and 12 month follow-ups compared to baseline
Insomnia Severity Index (ISI)
Change in ISI at post-treatment and 6 and 12 month follow-ups compared to baseline
Self-Rated Health (SRH-5)
Change in SRH-5 at post-treatment and 6 and 12 month follow-ups compared to baseline
Brunnsviken Brief Quality of life scale (BBQ)
Change in BBQ at post-treatment and 6 and 12 month follow-ups compared to baseline
EuroQoL-5 Dimension Questionnaire (EQ-5D)
Change in EQ5D at post-treatment and 6 and 12 month follow-ups compared to baseline
The Trimbos and Institute for Medical Technology Assessment Questionnaire on Costs Associated with Psychiatric Illness (TIC-P)
Change in TIC-P at post-treatment and 6 and 12 month follow-ups compared to baseline

Full Information

First Posted
January 23, 2017
Last Updated
March 16, 2021
Sponsor
Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT03051958
Brief Title
Internet-based Mindfulness and Exposure Treatment for Atopic Dermatitis
Official Title
Internet-based Mindfulness and Exposure Treatment for Atopic Dermatitis: Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
March 29, 2017 (Actual)
Primary Completion Date
June 28, 2019 (Actual)
Study Completion Date
June 28, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Atopic dermatitis (AD) is highly prevalent and leads to suffering for the individual, increased risk of depressive symptoms and anxiety, and high societal costs. A few psychological treatment have been tested for AD, but to our knowledge none of them have been built on recently developed methods for optimizing exposure treatment. In addition, access to psychological treatment is limited and there is a need for new methods that could be easily disseminated. One possible solution to this problem is to deliver psychological treatment via the Internet, which has been tested in more than 100 randomized trials with good results for other clinical disorders than AD. The aim of this study was to test the effects of Internet-delivered mindfulness and exposure treatment (I-MET) for AD in a randomized controlled trial. We hypothesized that I-MET would lead to larger reductions of AD symptoms as well as psychological symptoms compared to treatment as usual.
Detailed Description
Atopic dermatitis (AD), characterized by chronic itching and inflammation, is highly prevalent and leads to suffering for the individual, increased risk of depressive symptoms and anxiety, and high societal costs. Several behavioral factors are likely to play a role in the exacerbating AD symptoms over time, not least scratching, which may lead to rupture in the skin barrier and an increased risk of inflammation, which in turns increases AD symptoms. AD is also associated with avoidance behaviors that may have negative longer-term effects. With this in mind, psychological treatment based on exposure may be a logical method to achieve improvements. A few psychological treatments have been tested for AD, but to our knowledge none of them have been built on recently developed methods for optimizing exposure treatment. In a recently conducted pilot study we showed that exposure treatment, in combination with mindfulness training, can be associated with improvements for persons with AD. One challenge regarding psychological treatment is that accessibility is limited and there is a need for new methods that could be easily disseminated. One possible solution to this problem is to deliver psychological treatment via the Internet, which has been tested in more than 100 randomized trials with good results for other clinical disorders than AD. Internet-based treatment can be described as a form of online bibliotherapy where the individual is guided by a therapist who provides feedback on homework assignments. The aim of this study was to test the effects of Internet-delivered mindfulness and exposure treatment (I-MET) for AD in a randomized controlled trial. We hypothesized that I-MET would lead to larger reductions of AD symptoms as well perceived stress, sleep problems, depressive symptoms, general anxiety, and improved self-rated health, compared to treatment as usual. CLARIFICATION REGARDING STUDY START DATE (remark made on March 15, 2021): This trial employed one informed consent which was completed before the provision of screening data for the purpose of assessing eligibility. The first date on which a participant provided informed consent and screening data was Nov 27, 2016. The first date a participant was included in the study, as based on the assessment of eligibility criteria in accordance with the study protocol, was March 29, 2017. The latter date is considered to be the study start date, in accordance with 81 FR 65022.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
102 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Internet mindfulness&exposure treatment
Arm Type
Experimental
Arm Description
A 12-week treatment where the main treatment components are mindfulness, exposure and response prevention, a form of cognitive behavior therapy. The treatment entails methods to increase acceptance and non-reactivity to aversive thoughts and emotions associated with AD. The treatment is delivered via the Internet and comprises 10 modules, each with a specific theme. Throughout treatment, the patient is given structured exercises to work with on a daily basis.
Arm Title
Treatment as usual
Arm Type
Active Comparator
Arm Description
Participants receive information about moisturizer and anti-inflammatory lotion treatment which is treatment as usual. After 12 weeks, patients in this arm are crossed over to treatment.
Intervention Type
Behavioral
Intervention Name(s)
Internet mindfulness&exposure treatment
Other Intervention Name(s)
I-MET
Intervention Description
See description under "Arm".
Intervention Type
Other
Intervention Name(s)
Treatment as usual
Intervention Description
Written information about standard treatment for atopic dermatitis, that is information regarding how to use moisturizers and anti-inflammatory treatment such as Topical steroids.
Primary Outcome Measure Information:
Title
Patient-Oriented Eczema Measure (POEM)
Description
Change in POEM at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 9, week 10, week 11, post-treatment (12 weeks) , 6 month follow-up, 12 month follow-up
Secondary Outcome Measure Information:
Title
Visual analogue scale itch (VAS-itch)
Description
Change in VAS-scratch at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 9, week 10, week 11, post-treatment (12 weeks), weekly during treatment, 6 month follow-up, 12 month follow-up
Title
Visual analogue scale scratch (VAS-scratch)
Description
Change in VAS-scratch at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 9, week 10, week 11, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Visual analogue scale sleep (VAS-sleep)
Description
Change in VAS-sleep at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 9, week 10, week 11, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Dermatology Quality of Life Index (DLQI)
Description
Change in DLQI at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Beck Anxiety Inventory (BAI)
Description
Change in BAI at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Patient Health Questionnaire-9 (PHQ-9)
Description
Change in PHQ-9 at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Perceived stress scale (PSS)
Description
Change in PSS at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
5-dimensions itch scale (5-D itch scale)
Description
Change in 5-D itch scale at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Insomnia Severity Index (ISI)
Description
Change in ISI at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Self-Rated Health (SRH-5)
Description
Change in SRH-5 at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
Brunnsviken Brief Quality of life scale (BBQ)
Description
Change in BBQ at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
EuroQoL-5 Dimension Questionnaire (EQ-5D)
Description
Change in EQ5D at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Title
The Trimbos and Institute for Medical Technology Assessment Questionnaire on Costs Associated with Psychiatric Illness (TIC-P)
Description
Change in TIC-P at post-treatment and 6 and 12 month follow-ups compared to baseline
Time Frame
baseline, post-treatment (12 weeks), 6 month follow-up, 12 month follow-up
Other Pre-specified Outcome Measures:
Title
Client Satisfaction Questionnaire (CSQ-8)
Description
Mean and standard deviations will be presented
Time Frame
Post-treatment (12)
Title
Alcohol Disorders Identification Test (AUDIT)
Description
This measure is used only as a mean for gathering data regarding inclusion/exclusion criteria
Time Frame
Baseline
Title
Drug Use Disorders Identification Test (DUDIT)
Description
This measure is used only as a mean for gathering data regarding inclusion/exclusion criteria
Time Frame
Baseline
Title
Mediators using: Pain Reactivity Scale, Psychological Inflexibility in Pain Scale, Five Facets of Mindfulness- non reactivity scale, visual analogue scales for (itch, scratching and insomnia), and use of antiinflammatory skin creme
Description
Change in mediators from baseline to post-treatment (12 weeks) will be correlated with change in the primary outcome during the same time period
Time Frame
baseline, week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 9, week 10, week 11, post-treatment (12 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Fulfills the diagnostic criteria for atopic dermatitis in accordance with Williams criteria 1994 at the time of inclusion the eczema should be at least moderate according to The Patient Oriented Eczema Measure (POEM) Regular access to computer and internet connection If on antidepressant or regular sleep medication, the medication should be stable for at least one month prior to inclusion and the person should be willing to keep the medication stable throughout the study possibility to actively carry out the treatment (not go for longer journeys, do homework) good understanding of written and spoken Swedish Exclusion Criteria: severe psychiatric illness (bipolar disorder, schizophrenia or other psychotic illness, substance, alcohol abuse, severe depression, suicide risk) difficulties with reading or writing ongoing treatment for cancer pregnancy other psychological treatment that i ongoing or recently terminated stronger anxiety-reducing medication such as benzodiazepines treatment with antibiotics that is ongoing or has been terminated less than one month prior to inclusion Psoriasis UV-light treatment that is ongoing or has been terminated less than one month prior to inclusion oral treatment for eczema that is ongoing or has been terminated less than two month prior to inclusion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erik Hedman
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Institutet
City
Stockholm
ZIP/Postal Code
17177
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Karolinska Institutet requires that a formal assessment if the data can be made public must be conducted before publishing individual level data
Citations:
PubMed Identifier
34009282
Citation
Hedman-Lagerlof E, Fust J, Axelsson E, Bonnert M, Lalouni M, Molander O, Agrell P, Bergman A, Lindefors N, Bradley M. Internet-Delivered Cognitive Behavior Therapy for Atopic Dermatitis: A Randomized Clinical Trial. JAMA Dermatol. 2021 Jul 1;157(7):796-804. doi: 10.1001/jamadermatol.2021.1450.
Results Reference
derived

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Internet-based Mindfulness and Exposure Treatment for Atopic Dermatitis

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