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| ID | Type | Description | Link |
|---|---|---|---|
| K23AR078337 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) | NIH |
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PREP-Y | Experimental |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PREP-Y | Behavioral | The intervention is a series of behavioral health/psychoeducational modules that the participant will learn from. Participants will use the information discussed and overall impact on physical activity engagement, chronic pain management, and quality of life will be measured |
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility of Intervention | Fidelity checklists detailing content areas of the intervention adequately conveyed during the study visit will be used to measure intervention feasibility. | From enrollment to the post-treatment visit, for a total of 6 weeks |
| Acceptability of Intervention | Number of intervention visits completed by participants will be used to determine how acceptable the intervention is to the target population. | From enrollment to the post-treatment visit, for a total of 6 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Accelerometry Data | Activity from the Actigraphs will assist in understanding and identifying changes in participant physical activity. | From baseline to 3-month follow-up, for a total of 18 weeks |
| Functional Disability Inventory |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| William Black, PhD | Contact | 614-472-0717 | william.black@nationwidechildrens.org |
| Name | Affiliation | Role |
|---|---|---|
| William Black, PhD | Nationwide Children's Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nationwide Children's Hospital | Recruiting | Columbus | Ohio | 43205 | United States |
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| ID | Term |
|---|---|
| D059350 | Chronic Pain |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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The Functional Disability Inventory is a 15-item questionnaire that measures an individual's perception of how their illness limits their ability to complete regular activities. A higher score indicates a worse outcome.
| From baseline to 3-month follow-up, for a total of 18 weeks |