Skin Tracker: A Mobile Health App to Monitor Skin Disease Activity and Treatment Use

NCT ID: NCT04404075

Last Updated: 2024-01-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

11 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-04-25

Study Completion Date

2023-05-12

Brief Summary

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Design and beta-test a research-oriented mobile health app to assess disease activity, quality of life, treatment patterns, adverse medication effects, and lifestyle factors in patients with atopic dermatitis.

Detailed Description

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Mobile health technology, including smartphone apps and wearable monitors, has tremendous potential to transform clinical research. Recording of patient outcomes on a smartphone device and camera in the home setting can greatly reduce the number of in person research visits, saving tremendous costs, time, and effort associated with data entry. This also allows for easier recruitment of study subjects, who can be enrolled in geographic locations beyond academic research centers. After FDA approval of a therapy, mobile health technology can help researchers understand how that particular therapy is being used in a real-world setting, including frequency of use, adverse events, and impact of use on disease symptoms and patient quality of life. In this study, the investigators will create a mobile app to help the atopic dermatitis community understand the types of data and quality of data that can be gathered from atopic dermatitis patients longitudinally. A review of existing atopic dermatitis mobile apps on the market reveals they are consumer-oriented and may not be able to fully capture high-quality research data. The investigator proposed app is specifically geared for research, and thus fills an important gap. The research team will develop SkinTracker, a research-oriented eczema app to longitudinally track atopic dermatitis severity, symptoms, quality of life, physical activity, medication usage, and adverse events in a real-world setting.

Conditions

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Atopic Dermatitis Eczema

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Group 1 patients

1. Age 18 and above
2. Eczema Area and Severity Index (EASI) score ≥ 10
3. Investigator Global Assessment (IGA) ≥ 3

SkinTracker Mobile App

Intervention Type OTHER

a research-oriented eczema app to longitudinally track atopic dermatitis severity, symptoms, quality of life, physical activity, medication usage, and adverse events in a real-world setting

Group 2 patients

1. Age 18 and above
2. Eczema Area and Severity Index (EASI) score ≥ 1 but \< 10
3. Investigator Global Assessment (IGA) 1 or 2

SkinTracker Mobile App

Intervention Type OTHER

a research-oriented eczema app to longitudinally track atopic dermatitis severity, symptoms, quality of life, physical activity, medication usage, and adverse events in a real-world setting

Group 3 patients

1. Age 12 to 17
2. Eczema Area and Severity Index (EASI) score ≥ 10
3. Investigator Global Assessment (IGA) ≥ 3

SkinTracker Mobile App

Intervention Type OTHER

a research-oriented eczema app to longitudinally track atopic dermatitis severity, symptoms, quality of life, physical activity, medication usage, and adverse events in a real-world setting

Group 4 patients

1. Age 12 to 17
2. Eczema Area and Severity Index (EASI) score ≥ 1 but \< 10
3. Investigator Global Assessment (IGA) 1 or 2

SkinTracker Mobile App

Intervention Type OTHER

a research-oriented eczema app to longitudinally track atopic dermatitis severity, symptoms, quality of life, physical activity, medication usage, and adverse events in a real-world setting

Interventions

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SkinTracker Mobile App

a research-oriented eczema app to longitudinally track atopic dermatitis severity, symptoms, quality of life, physical activity, medication usage, and adverse events in a real-world setting

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Ability to provide written informed consent and comply with the protocol.
2. At least 13 years of age.
3. Diagnosis of atopic dermatitis by dermatologist for at least 6 months.
4. Physical exam within clinically acceptable limits.
5. Own or have access to a mobile device that is compatible with study mobile application SkinTracker.

Exclusion Criteria

1. Subject is unable to provide written informed consent or comply with the protocol.
2. Unable to input data into SkinTracker mobile app.
3. Subject is younger than 13 years of age.
4. Serious known infection.
5. History of immunosuppression (including human immunodeficiency virus (HIV)).
6. History of malignancy within 5 years prior to screening visit, except completely treated in situ carcinoma of the cervix, completely treated and resolved non-metastatic squamous or basal cell carcinoma of the skin.
7. Severe concomitant illness.
8. Physical exam not within clinically acceptable limits.
9. Subjects possess other diagnoses that, in the investigator's opinion, preclude him/her from safely participating in this study or interfere
Minimum Eligible Age

13 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of California, San Francisco

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Wilson Liao, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Locations

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UCSF Psoriasis and Skin Treatment Center

San Francisco, California, United States

Site Status

Countries

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United States

Other Identifiers

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19-28676

Identifier Type: -

Identifier Source: org_study_id

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