Itch pruritus
Conditions
Interventions
None listed
Sponsors
Universiteit Leiden
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Healthy human volunteers, 18 - 35 year old, fluent in Dutch language
Exclusion criteria
Exclusion criteria: Severe morbidity (e.g., multiple sclerosis, diabetes mellitus, heart or lung diseases), psychiatric disorders (e.g., depression), use of pacemaker, color-blindness, diagnose of histamine hypersensitivity, and chronic itch or pain complaints.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study endpoint is the difference in the levels of itch (VAS scores) evoked by the electrical stimuli associated with the conditioned cues versus the neutral cues in the testing phase of part II of the experiment. It is investigated whether nocebo effects (negative expectation effects) can be modified by a positive expectation induction by conditioning and verbal suggestion (low-itch expectation induction) (group 1), resulting in lower itch VAS scores than a repeated negative expectation induction (high-itch expectation induction) (group 2), or a neutral procedure (neutral expectation induction) (group 3). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary study endpoints of the present experiment are: a) the itch related expectancy effects on scratching behavior; b) the itch related expectancy effects regarding itch evoked by histamine iontophoresis; c) the role of individual characteristics (e.g., optimism) on (the modifiability) of expectancy effects; and d) the role of 5-HTTLPR genotype and other genetic variants on (the modifiability) of expectancy effects. | — |
Countries
Netherlands
Outcome results
None listed