Survey on Sensory Processing Sensitivity in Chronic Pediatric Pain

Chronic Pain Clinical Trial

Official title:

Towards a Deeper Understanding of Chronic Pediatric Pain: Exploring the Role of Sensory Processing Sensitivity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04171869
• Other study ID #: Sensory Processing Sensitivity
• Status: Completed
• Start date: May 8, 2020
• Est. completion date: September 30, 2020

Study information

• Verified date: September 2020
• Source: University Hospital, Basel, Switzerland
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Background: Pain is defined as an unpleasant sensory and emotional experience and in its chronic form, pain is highly prevalent, up to 25% of children and adolescents are affected by it. The exact etiology of many forms of chronic pain remains unknown. One mechanism that has been proposed to underlie increased pain sensitivity is central sensitization, i.e., increased efficacy of the nervous system in transmitting pain signals, which manifests itself as a lower pain threshold. A lower pain threshold in turn has been recognized as a risk factor for the development of chronic pain. Being more sensitive to pain is one feature commonly shared by those with high sensory processing sensitivity (SPS), who are thought to react more strongly to both positive and negative environmental influences. The relationship between this increased sensitivity and pain tolerance has not been studied to date, but could contribute to our understanding of why some children and adolescents are more vulnerable to developing chronic pain than others.

Objectives and Aims: The aim of this project is to increase scientific understanding of 1) the distribution and correlates of high SPS among children and adolescents suffering from chronic pain, and 2) whether the trait of SPS can help explain increased pain sensitivity and hence vulnerability for chronic pain.

Methods: To determine the distribution (aim 1a) and correlates (aim 1b) of SPS among a population of children and adolescents suffering from chronic pain, an online survey will be conducted. Participants will be asked to complete questionnaires about their SPS as well as pain history and pain characteristics. The distribution of SPS will then be compared to an existing distribution in a sample of healthy children and adolescents.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: September 30, 2020
• Est. primary completion date: August 15, 2020
• Gender: All
• Age group: 17 Years to 19 Years

Eligibility

Inclusion Criteria:

• Adolescents aged 17-19 years

• Persistent or recurrent pain for 3 months or more

• Fluent in German or English

Exclusion Criteria:

• Younger than 17 or older than 19 years

• Acute pain

Related Conditions & MeSH terms

• Chronic Pain

Intervention

Other:
• no intervention
observational study, no intervention

Locations

Country	Name	City	State
Switzerland	Faculty of Psychology, University of Basel	Basel

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Highly Sensitive Child Scale	Sensory Processing Sensitivity	through study completion, an average of 6 months
Primary	Functional Disability Inventory for children	Physical functioning and disability in children with chronic pain	through study completion, an average of 6 months