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Empowered Relief for Youth (ER-Y)

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Stanford University

Status

Completed

Conditions

Complex Regional Pain Syndromes
Musculoskeletal Pain
Fibromyalgia
Neuropathic Pain
Chronic Pain
Abdominal Pain

Treatments

Behavioral: Empowered Relief for Youth

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this pilot study is to examine the feasibility and preliminary efficacy of Empowered Relief for Youth with chronic pain (ER-Y). ER-Y is a single-session pain management class for youth focused on pain science education and teaching self-regulatory skills for pain management based on the evidence-based adult ER class. Feasibility and acceptability of ER-Y will be assessed post-class. Preliminary efficacy will be assessed by administering surveys at baseline, 4-weeks, 8-weeks, and 12-weeks post class.

Full description

The current proposed, single-arm, uncontrolled pilot study will determine a) feasibility of ER-Y in youth with chronic pain, b) patients' perceptions and satisfaction of the ER-Y class and c) preliminary efficacy to inform the design of a subsequent randomized controlled trial.

Enrollment

110 patients

Sex

All

Ages

10 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age at least 10 years old to 18 years
  • Diagnosis of Chronic Pain
  • English speaking

Exclusion criteria

  • Significant psychosocial complexity (e.g., severe depression/ anxiety, unable to tolerate a group setting)
  • non-English Speaking

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

110 participants in 1 patient group

Empowered Relief for Youth
Experimental group
Description:
Empowered Relief for Youth is a single-session pain management class focused on pain science education and teaching self-regulatory skills for pain management based on the evidence-based adult ER class.
Treatment:
Behavioral: Empowered Relief for Youth

Trial contacts and locations

1

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Central trial contact

Nicole Jehl, BS; Jeremy Giberson, MAS

Data sourced from clinicaltrials.gov

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