Effectiveness of a Digital Treatment for Adolescents with Chronic Pain

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

195 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-10-31

Study Completion Date

2027-12-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Chronic Pain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Digital treatment

The treatment includes a smartphone-based psychosocial program designed to improve the quality of life of adolescents with chronic pain.

Group Type EXPERIMENTAL

Self-administered psychosocial intervention delivered via smartphone.

Intervention Type BEHAVIORAL

The treatment includes a smartphone-based psychosocial program designed to improve the quality of life of adolescents with chronic pain.

Interventions

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Self-administered psychosocial intervention delivered via smartphone.

The treatment includes a smartphone-based psychosocial program designed to improve the quality of life of adolescents with chronic pain.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.