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Conditioning, the Placebo Effect, and Psoriasis

Primary Purpose

Psoriasis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Partial schedule of pharmacotherapeutic reinforcement
Dose control for Arm B
Standard pharmacotherapeutic protocol
Sponsored by
University of Rochester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psoriasis focused on measuring Conditioning, Corticosteroid, Lesions, Pharmacotherapy, Placebo effect, Psoriasis, Psychoneuroimmunology

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Arm Type

Experimental

Experimental

Experimental

Arm Label

A

B

C

Arm Description

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.

Outcomes

Primary Outcome Measures

Routine and standard quantitative and qualitative assessment of plaque changes and growth
Severity Index, clinically described as to redness, flaking and thickness on a total scale of 9

Secondary Outcome Measures

Impacts of Events Scale (IES)
Psoriasis Life Stress Inventory) (PLSI)
Hassles Scale
Interpersonal Support Evaluation List (ISEL)

Full Information

First Posted
June 22, 2000
Last Updated
September 20, 2013
Sponsor
University of Rochester
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
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1. Study Identification

Unique Protocol Identification Number
NCT00005922
Brief Title
Conditioning, the Placebo Effect, and Psoriasis
Official Title
Role of Conditioning in the Pharmacotherapy of Psoriasis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
August 2000 (undefined)
Primary Completion Date
July 2006 (Actual)
Study Completion Date
July 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Rochester
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study uses the psychological principle known as classical conditioning to try to improve the standard treatment of psoriasis. Classical conditioning is a process of behavioral modification in which a person learns to connect a certain response-in this case, improvement of psoriasis-with a new action, or stimulus-in this case, application of an inactive cream. The goal of this study is to show that people with psoriasis who are maintained on corticosteroid cream part of the time and an inactive (placebo) cream at other times show a lower incidence of relapse and a reduced severity of psoriasis that patients treated with that same (reduced) amount of medication administered all the time.
Detailed Description
The lack of scientific attention devoted to the placebo effect as a phenomenon in its own right probably reflects the paucity of theoretical positions within which to organize the existing data and design new research. This research addresses the clinical significance of behavior-immune system interactions. This study will capitalize on conditioned immunosuppressive responses to reduce the cumulative amount of corticosteroid medication used in the treatment of psoriasis. We will continue to treat patients with steroid, but will shift experimental patients from their current schedule of continuous reinforcement (active drug whenever medication is applied) to a partial schedule of reinforcement (active drug a percentage of the time and placebo alone at other times). To equate amount of medication, we will treat another group of patients with a reduced dose of steroid in a standard treatment regimen (continuous schedule of reinforcement). We hypothesize that, holding cumulative dose constant, a partial schedule of reinforcement will enable patients to be maintained on lower cumulative amounts of corticosteroid than patients treated under a continuous schedule of active drug. This is the first attempt to adopt conditioning principles and use schedules of reinforcement to design regimens of drug therapy. If proven effective, this new approach to pharmacotherapy and placebo effects is likely to stimulate new interdisciplinary research in neuropharmacology and behavioral pharmacology for the treatment of autoimmune disorders and a variety of other chronic diseases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psoriasis
Keywords
Conditioning, Corticosteroid, Lesions, Pharmacotherapy, Placebo effect, Psoriasis, Psychoneuroimmunology

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
138 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Participants will receive 100% of the dose of the medication on the same reinforcement schedule (100%) as received during the baseline (maintenance) period.
Arm Title
B
Arm Type
Experimental
Arm Description
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
Arm Title
C
Arm Type
Experimental
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Partial schedule of pharmacotherapeutic reinforcement
Other Intervention Name(s)
Aristocort A
Intervention Description
Dose of 0.1% of Aristocort A on 1-2 of every 4 days for a period of up to 14 weeks.
Intervention Type
Drug
Intervention Name(s)
Dose control for Arm B
Other Intervention Name(s)
Aristocort A
Intervention Description
Dose of 0.025-0.05% of Aristocort A 2 times per day for a period of up to 14 weeks.
Intervention Type
Other
Intervention Name(s)
Standard pharmacotherapeutic protocol
Other Intervention Name(s)
Aristicort A
Intervention Description
Full dose of Aristicort A (0.1%) 2 times per day for a period of up to 14 weeks.
Primary Outcome Measure Information:
Title
Routine and standard quantitative and qualitative assessment of plaque changes and growth
Time Frame
Weekly
Title
Severity Index, clinically described as to redness, flaking and thickness on a total scale of 9
Time Frame
Weekly
Secondary Outcome Measure Information:
Title
Impacts of Events Scale (IES)
Time Frame
Once - at the initial start of the study
Title
Psoriasis Life Stress Inventory) (PLSI)
Time Frame
Weekly
Title
Hassles Scale
Time Frame
Weekly
Title
Interpersonal Support Evaluation List (ISEL)
Time Frame
Once - at the intial start of the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Ader, PhD
Organizational Affiliation
University of Rochester
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University
City
Palo Alto
State/Province
California
ZIP/Postal Code
94305
Country
United States
Facility Name
Adult Dermatology Clinic, Strong Memorial Hospital
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
1162023
Citation
Ader R, Cohen N. Behaviorally conditioned immunosuppression. Psychosom Med. 1975 Jul-Aug;37(4):333-40. doi: 10.1097/00006842-197507000-00007.
Results Reference
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PubMed Identifier
7815892
Citation
Ader R, Cohen N, Felten D. Psychoneuroimmunology: interactions between the nervous system and the immune system. Lancet. 1995 Jan 14;345(8942):99-103. doi: 10.1016/s0140-6736(95)90066-7. No abstract available.
Results Reference
background
PubMed Identifier
9081556
Citation
Giang DW, Goodman AD, Schiffer RB, Mattson DH, Petrie M, Cohen N, Ader R. Conditioning of cyclophosphamide-induced leukopenia in humans. J Neuropsychiatry Clin Neurosci. 1996 Spring;8(2):194-201. doi: 10.1176/jnp.8.2.194.
Results Reference
background
Citation
Ader R. "The role of conditioning in pharmacotherapy." In The placebo effect: An interdisciplinary exploration, edited by A. Harrington, 138-165. Cambridge: Harvard University Press, 1997.
Results Reference
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Conditioning, the Placebo Effect, and Psoriasis

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