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Stress-induced Scratching in Healthy and AD

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University of Miami

Status

Completed

Conditions

Atopic Dermatitis
Healthy

Treatments

Behavioral: Trier Social Stress Test (TSST)
Behavioral: Landscape Video

Study type

Interventional

Funder types

Other

Identifiers

NCT04174651
20190833

Details and patient eligibility

About

The purpose of this study is to examine scratching behavior and identify brain areas responsible for stress-induced spontaneous scratching in patients with atopic dermatitis (AD).

Enrollment

8 patients

Sex

All

Ages

18 to 59 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Healthy subjects and AD patients between 18 and 59 years of age.
  2. Healthy subjects: In general, good health without history of neurological and psychiatric diseases.
  3. AD patients: An average itch rating of 3 out of 10 or greater in the past two weeks using a Numerical Rating Scale (NRS).
  4. All patients will be required to cease use of oral antihistamines from the night before each study visit until the end of the experiment. The purpose is to avoid that participants fall asleep during MRI measurement due to side effect oral antihistamine (i.e., sedation).
  5. Women of child bearing potential will be administered a pregnancy test to verify that they are not pregnant.
  6. MRI Compatibility, criteria include having no major contraindication for MRI (pacemaker, vascular stents, metallic ear tubes, and absence of metal implants or braces) as assessed by MRI technologist using site approved screening form.
  7. Participants have to be able to speak and read English fluently.
  8. Participants must have signed a written informed consent before being enrolled in the study

Exclusion criteria

  1. Individuals under 18 or over 59 years of age.
  2. Inability to complete the required measures.
  3. Suffering from any disease state or physical condition, which would increase their health risk by study participation.
  4. Currently enrolled in any investigational study in which the subject is receiving any type of drug, biological, or non-drug therapy.
  5. Recent initiation (within last 3 months) of centrally acting agents such as antidepressants, neuroleptics or neuropathic medications.
  6. Patients who use centrally acting agents only when they need. The purpose is to avoid a risk of acute effect of these agents on brain activity and perceived stress due to the stress task.
  7. Current treatment with opioid analgesics.
  8. Uncontrolled thyroid disease.
  9. Use of illicit drugs or history of opiate addiction.
  10. Diagnosis of a major psychiatric disorder such as schizophrenia, major depression or bipolar disorder that is active right now.
  11. Any known diseases or disorders that may affect conducting the experiments (e.g., intracranial pathology, claustrophobia, severe respiratory or cardiovascular problems, active fibromyalgia) or diseases that have potential risks of infections (e.g., HIV, Hepatitis C, etc).
  12. Inability to speak and read English.
  13. Being pregnant.
  14. Incarcerated.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

8 participants in 2 patient groups

Participants with AD with MRI
Experimental group
Description:
Participants that are diagnosed with AD will receive both the acute stress condition (TSST) and the control condition (watching a landscape video). The order when the 2 conditions will be provided is randomized per participant and completed 2 weeks apart. These subjects will be evaluated with MRI.
Treatment:
Behavioral: Landscape Video
Behavioral: Trier Social Stress Test (TSST)
Healthy Participants with MRI
Experimental group
Description:
Healthy participants will receive both the acute stress condition (TSST) and the control condition (watching a landscape video). The order when the 2 conditions will be provided is randomized per participant and completed 2 weeks apart. These subjects will be evaluated with MRI.
Treatment:
Behavioral: Landscape Video
Behavioral: Trier Social Stress Test (TSST)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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