Texting patients could boost psoriasis drug success
NCT ID NCT05570955
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether weekly text reminders help people with psoriasis take their deucravacitinib medication as prescribed. Forty patients will be split into two groups: one gets reminders, the other does not. Researchers will interview participants to understand what helps or hinders sticking to the treatment, and compare skin improvement between those who take the drug regularly and those who don't.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- deucravacitinib
- What this could lead to
- If successful, this could show that simple text reminders help people take their psoriasis medication more consistently, leading to better real-world results.
- What could go wrong
- This is a small, early-stage study with only 40 participants, so findings may not apply to everyone. It focuses on adherence behavior, not on whether the drug itself works better.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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40 people
The number who actually took part.
- Started
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Jul 2023
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with moderate-to-severe plaque psoriasis. Standard criteria for moderate-to-severe plaque psoriasis will be used (BSA greater than or equal to 3% or face/palm/sole/genital involvement or severe effect on Quality of Life). * Subject must be 18 years of age or older. * Subject must have a working knowledge of English. * Approved birth control methods required for females of childbearing potential. * Baseline TB test. Exclusion Criteria: * Patients without a diagnosis of moderate-to-severe plaque psoriasis. * Patients under 18 years of age. * Patients with severe or unstable comorbid conditions. * Patients with active malignancy or malignancy in past 5 years (not including appropriately treated cutaneous basal and cutaneous-limited squamous cell carcinomas). * Patients who are pregnant or breastfeeding. * Patients with any other skin condition that prohibit or confound the ability of the investigator to interpret skin findings. * Patients with active substance or alcohol abuse disorder; or history of substance/alcohol abuse disorder within 6 months prior to study enrollment. * History of, or active, severe depression and/or suicidality. * Patients with active or latent tuberculosis as determined by quant-TB baseline testing * Patients that are taking concomitant biologics, systemics for the treatment of psoriasis and/or phototherapy.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Wake Forest University Health Sciences Department of Dermatology
Winston-Salem, North Carolina, 27157, United States
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