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Testing a method to improve patient adherence to the doctors treatment plan for topically treated psoriasis

A designed Patient-centered Intervention to Improve medical Adherence in Topical Treatment of psoriasis - A Study protocol

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2016-002143-42-DK
Enrollment
134
Registered
2016-06-01
Start date
2017-11-08
Completion date
Unknown
Last updated
2021-01-11

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

Conditions

Psoriasis MedDRA version: 19.1 Level: PT Classification code 10037153 Term: Psoriasis System Organ Class: 10040785 - Skin and subcutaneous tissue disorders

Interventions

Trade Name: Enstilar, kutanskum Product Code: 55716 Pharmaceutical Form: Cutaneous spray Other descriptive name: CALCIPOTRIOL MONOHYDRATE Concentration unit: µg microgram(s) Concentration type: equal

Sponsors

Odense University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Psoriasis patients aged 18-75 years diagnosed with mild-to moderate psoriasis. Patients need to have a smartphone and basic user skills for the smartphone Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 106 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 28

Exclusion criteria

Exclusion criteria: aged under 18 and above 75 years, severe degrees of psoriasis, i.e. pustular and erythrodermic psoriasis, lack of smartphones and user skills for the smartphone.

Design outcomes

Primary

MeasureTime frame
Main Objective: Test if an app for smartphones can improve Medical adherence in psoriasis patients;Secondary Objective: Test if improved medical adherence can improve quality of life and reduce severity of disease;Primary end point(s): rate of secondary medical adherence;Timepoint(s) of evaluation of this end point: week 4.

Secondary

MeasureTime frame
Secondary end point(s): DLQI (dermatology life quality index) and LS-GPA (lattice-system physician global assessment);Timepoint(s) of evaluation of this end point: baseline, week 4, week 8 and week 26

Countries

Denmark

Contacts

Public ContactMathias Tiedemann Svendsen

Odense University Hospital

mathias.tiedemann.svendsen@rsyd.dk+4565413239

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026