Treatment Options for Pediatric Chronic Pain: How do we Best Disseminate Our Scientific Findings

NCT ID: NCT05239299

Last Updated: 2025-02-03

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

COMPLETED

Total Enrollment

19 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-05-21

Study Completion Date

2024-12-31

Brief Summary

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Pediatric chronic pain is a prevalent condition with manifold treatment options. However, knowledge of targeted dissemination of intervention research findings is currently lacking.

The aim of this project is to determine satisfaction with current knowledge transfer from science to clinical practice amongst health care professionals, adolescents with CPP and their parents and to understand what treatment options have been offered to patients in Swiss pain centers Three focus groups, one with health care professionals, one with adolescent patients, and one with their parents, will be conducted to determine how the dissemination of scientific evidence to clinical practice can be improved and what hurdles exists when gathering information about pain interventions. In addition, patients will be asked about the treatment options offered to them and health care professionals about which treatments they routinely prescribe and why.

Detailed Description

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Conditions

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Pediatric Chronic Pain

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Adolescents with chronic pain

No intervention, observational study

Intervention Type OTHER

Focus Group

Parents of adolescents with chronic pain

No intervention, observational study

Intervention Type OTHER

Focus Group

Health care professionals who work with adolescents with chronic pain

No intervention, observational study

Intervention Type OTHER

Focus Group

Interventions

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No intervention, observational study

Focus Group

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Adolescent group:

* Adolescents suffering from chronic pain (i.e., persistent or recurrent pain for three months or more)
* Able to read and speak German

Parent group:

* Parents of an adolescent with chronic pain
* Able to read and speak German

Health care professionals group:

* Health care professional working with adolescents with chronic pain
* Able to read and speak German

Exclusion Criteria

* no chronic pain or experience with chronic pain
Minimum Eligible Age

13 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Basel, Switzerland

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Helen Koechlin, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Basel

Locations

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Faculty of Psychology, University of Basel

Basel, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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Dissemination Focus Groups

Identifier Type: -

Identifier Source: org_study_id

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