Actively Recruiting

Age: 5Years - 17Years
All Genders
Healthy Volunteers
NCT06659731

Quantitative Sensory Testing to Study Pain Perception in Autism

Led by IRCCS Eugenio Medea · Updated on 2024-10-26

50

Participants Needed

1

Research Sites

58 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims at assess sensory perception, and pain perception, in neurodivergent children and adolescent in the autism spectrum. To achieve this goal, the quantitive sensory testing (QST), a controlled and replicable protocol, will be used, to assess perception in different sensory modalities: heat sensations, mechanical detection threshold and pain threshold. As secondary aim, the cortical processing of thermal painful stimuli will be collected through electroencephalography (EEG) in order to investigate if there are differences in the cortical processing of painful stimuli between clinical sample and control sample, and if it could be associated with differences in the subjective experience between the two groups. Finally, it will be explored the association between such differences, and indexes of psychopathology and dispositional measures.

CONDITIONS

Official Title

Quantitative Sensory Testing to Study Pain Perception in Autism

Who Can Participate

Age: 5Years - 17Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children and adolescents aged between 5 and 17 years old
  • Autism diagnosis according to DSM-V criteria (clinical sample)
  • Healthy children and adolescents without neurological or psychiatric diagnoses (control sample)
Not Eligible

You will not qualify if you...

  • Peripheral neuropathies
  • Psychiatric diagnoses such as psychosis
  • Tourette Syndrome
  • Neurological diagnoses such as epilepsy
  • Sensory deficit or loss
  • Genetic diseases

AI-Screening

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Trial Site Locations

Total: 1 location

1

IRCCS "E. Medea"

Brindisi, BR, Italy, 72100

Actively Recruiting

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Research Team

V

Valentina Nicolardi, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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