Conditioning, the Placebo Effect, and Psoriasis
Psoriasis
About this trial
This is an interventional treatment trial for Psoriasis focused on measuring Conditioning, Corticosteroid, Lesions, Pharmacotherapy, Placebo effect, Psoriasis, Psychoneuroimmunology
Eligibility Criteria
Inclusion Criteria: Psoriasis patients with mild to moderate lesions who are able to attend weekly clinic visits at either the University of Rochester School of Medicine and Dentistry in Rochester, NY, or Stanford University in Palo Alto, CA. Patients must be in good health (as determined by prescreening examination). Patients must not be using systemic treatment (for example, oral medications) or intralesional, UV, or topical therapies except bland emollients for at least 2 weeks before the start date of the study. Patients must have chronic, stable plaque psoriasis with a score of greater than or equal to 7 on a routine 9-point Severity Index. Exclusion Criteria: Use of immunosuppressive medication within the past 2 months. Pregnant or sexually active women who do not use contraceptives. Patients who cannot be monitored regularly. History of allergy to corticosteroid or other study ointment components. Patients who have more than 10 percent of body surface area covered by psoriatic lesions.
Sites / Locations
- Stanford University
- Adult Dermatology Clinic, Strong Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
A
B
C
Participants will receive 100% of the dose of the medication on the same reinforcement schedule (100%) as received during the baseline (maintenance) period.
Participants will receive 100% of the dose of the medication on a partial reinforcement schedule (25% or 50%) as received during the baseline (maintenance) period
Participants will receive 25% or 50% of the dose of the medication on the same reinforcement schedule (100%) as received during the baseline (maintenance) period.