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Physical Activity Pain Resilience (PAPR)

W

William Black

Status

Enrolling

Conditions

Chronic Pain

Treatments

Behavioral: PREP-Y

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07049029
STUDY00004982
K23AR078337 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this research study is to test a new program called Pain REsilience Promotion for Youth (PREP-Y). This program is designed to help adolescents with chronic musculoskeletal pain (pain in muscles, bones, or joints that lasts more than 3 months) become more physically active and better able to manage their pain. The program includes four weekly virtual sessions that teach skills related to resilience, such as how to stay motivated, build confidence, and cope with pain.

Participants will complete surveys and physical activity tests before and after the program. Participants will also wear physical activity monitors to track their activity levels. The goal of this study is to learn whether the program is practical, helpful, and acceptable to participants, and to prepare for a future larger study.

Enrollment

30 estimated patients

Sex

All

Ages

12 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Between the ages of 12 and 17
  • History of chronic musculoskeletal pain for more than 3 months assessed by a pediatric rheumatologist or pain physician
  • Diagnosis of a primary pain disorder (e.g., juvenile fibromyalgia and other widespread pain conditions, lower back pain, complex regional pain and amplified pain syndrome)
  • Speaks English as primary language

Exclusion criteria

  • Chronic pain secondary to disease (e.g., sickle cell disease or rheumatic disease such as juvenile arthritis, systemic lupus erythematosus)
  • Presence of an untreated major psychiatric diagnosis (e.g., major depression, bi-polar disorder, psychoses)
  • History or diagnosis of developmental delay.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

PREP-Y
Experimental group
Treatment:
Behavioral: PREP-Y

Trial contacts and locations

1

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Central trial contact

William Black, PhD

Data sourced from clinicaltrials.gov

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