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Clinical Trials/NCT06765200
NCT06765200
Not yet recruiting
Not Applicable

Effectiveness of a Digital Treatment for Adolescents with Chronic Pain

University Rovira i Virgili1 site in 1 country195 target enrollmentOctober 2025
ConditionsChronic Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
University Rovira i Virgili
Enrollment
195
Locations
1
Primary Endpoint
Pain intensity
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Research has shown that the prevalence of chronic pain in adolescents is high and increasing. These young people report significant changes in both their physical and psychological functioning. Currently, psychosocial treatments enjoy strong empirical support and are crucial to maintaining and improving the quality of life of adolescents suffering from chronic pain. However, the availability of these evidence-based interventions is insufficient to meet the high demand, especially outside of large cities. The aim of this project is to develop a digital treatment that helps improve the quality of life of adolescents with chronic pain and complementary websites for their parents and teachers.

Registry
clinicaltrials.gov
Start Date
October 2025
End Date
December 2027
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Rovira i Virgili
Responsible Party
Principal Investigator
Principal Investigator

Jordi Miró

Professor

University Rovira i Virgili

Eligibility Criteria

Inclusion Criteria

  • 12-18 years old,
  • Having a non-oncology secondary chronic pain problem,
  • Having internet access,
  • A parent willing to participate in the study,
  • Providing informed consent/assent.

Exclusion Criteria

  • Cognitive or language problems

Outcomes

Primary Outcomes

Pain intensity

Time Frame: baseline, 8 weeks, 3 months follow-up

Refers to the severity of pain an individual experiences, measured on a scale (0-10)

Pain interference

Time Frame: baseline, 8 weeks, 3 months follow-up

Refers to the extent to which pain affects an individual's daily life and functioning. Patient-Reported Outcomes Measurement Information System (PROMIS) Pediatric Pain Interference will be used (0-32; 0=no interference, 32=intense interference).

Global perception of change after treatment

Time Frame: 8 weeks, 3 months follow-up

refers to an individual's overall assessment of how their condition has improved or worsened following a treatment, measured on a scale (0-10).

Study Sites (1)

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