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The impact of a new model of chronic disease management based on digital therapy on patients with atopic dermatitis, psoriasis, and vitiligo: A randomized controlled study.

The impact of a new model of chronic disease management based on digital therapy on patients with atopic dermatitis, psoriasis, and vitiligo: A randomized controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120901
Enrollment
Unknown
Registered
2026-03-22
Start date
2025-05-28
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Atopic dermatitis, psoriasis, vitiligo

Interventions

Trial Group:Use of intelligent platform medical companion for continuous follow-up, including but not limited to medical education, medication guidance, treatment reminders, and nutritional support, a
Control Group:No use of intelligent management platform
routine follow-up visits with feedback on medication adherence and adverse reactions

Sponsors

Shenzhen People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Be 18 years of age or older; 2. Patients who have been clinically diagnosed with atopic dermatitis, psoriasis, vitiligo, and plan to receive treatment or are being treated; 3. The patient is able to understand the purpose of the trial, voluntarily participate in and sign the informed consent form, and is willing to complete the follow-up according to the requirements of the protocol; 4. Be aware and be able to answer questions correctly; 5. Be proficient in using a smartphone or complete software download and project transfer feedback with the help of relatives.

Exclusion criteria

Exclusion criteria: 1. Have a serious underlying medical condition or poor physical condition; 2. Pregnant or lactating women; 3. Unable to receive treatment due to the patient's refusal or organ function, complications, etc.; 4. Participate in other clinical trials at the same time; 5. Lack of information such as past medical history, examination and examination, and treatment status; 6. Patient refuses to provide data or refuses to participate in the study; 7. Other situations judged by the investigator to be inappropriate to participate.

Design outcomes

Primary

MeasureTime frame
Dermatology Life Quality Index (DLQI);

Secondary

MeasureTime frame
Dermatology Life Quality Index (DLQI);Dermatology Life Quality Index (DLQI);Dermatology Life Quality Index (DLQI);Psoriasis Area and Severity Index (PASI);Psoriasis Area and Severity Index (PASI);Psoriasis Area and Severity Index (PASI);Eczema Area and Severity Index (EASI);Eczema Area and Severity Index (EASI);Eczema Area and Severity Index (EASI);Total Vitiligo Area Scoring Index (T-VASI);Total Vitiligo Area Scoring Index (T-VASI);Total Vitiligo Area Scoring Index (T-VASI);Facial Vitiligo Area Scoring Index (F-VASI);Facial Vitiligo Area Scoring Index (F-VASI);Facial Vitiligo Area Scoring Index (F-VASI);

Countries

China

Contacts

Public ContactZhang Jianglin

Shenzhen People's Hospital (First Affiliated Hospital of Southern University of Science and Technology; Second Clinical Medical College of Jinan University)

zhang.jianglin@szhospital.com+86 138 7314 3466

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026