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NCT07249931 · ClinicalTrials.gov registry record · NA

Efficacy and Safety of Nerivio for the Management of Amplified Musculoskeletal Pain Syndrome in Pediatric Patients

A NA study, sponsored by Children's Health.

Not yet
Registry status
NA
Development phase
40
Enrollment target

NCT07249931 is a NA study that has not yet begun recruiting, run by Children's Health. The registered enrollment target is 40 participants.

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The verdict

NCT07249931, a NA study, has not yet begun recruiting, sponsored by Children's Health.

NOT YET RECRUITING
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

The goal of this trial is to learn how the Nerivio® device works to treat Amplified Musculoskeletal Pain Syndrome (AMPS) in children ages 8-18. Nerivio® is a wearable device that activates specific nerves in the upper arm. This causes a response from the brain that has been helpful for people who experience migrane headaches. The main questions this study aims to answer are: * How well does the Nerivio® device help in reducing pain in children with AMPS? * Does the use of the Nerivio® device help improve quality of life in children with AMPS? * How satisfied are children and their families with the use of the Nerivio® device for treatment of AMPS? Researchers will compare the use of the Nerivio® device with usual treatment for AMPS (including pain medications, physical therapy, and other interventions) to see how well the Nerivio® device helps control pain. Participants will be in one of two groups, decided by: * Those who are in the "control" group will use their usual practices to control pain. * Those who are in the "intervention" group will use the Nerivio® device once every other day. All participants in the "control group" will: * Complete surveys and answer questions about their pain and how it affects their daily life * Use their existing methods for pain control. All participants in the "intervention" group will: * Complete surveys and answer questions about their pain and how it affects their daily life * Learn how to work the Nerivio® device and smartphone app. * Use the Nerivio® device every other day (every 48 hours).

Interventions

  • OTHER Usual Care
  • DEVICE Nerivio(R) Device

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2025-12-01
Est. Completion 2028-12-31
Phase NA

Sponsor

Children's Health

4 total trials

What the Registry Record Tells You About NCT07249931

The ClinicalTrials.gov registry entry for NCT07249931 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Health, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Usual Care is the first listed.

NCT07249931 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07249931 about?

NCT07249931 is a clinical study titled "Efficacy and Safety of Nerivio for the Management of Amplified Musculoskeletal Pain Syndrome in Pediatric Patients". The goal of this trial is to learn how the Nerivio® device works to treat Amplified Musculoskeletal Pain Syndrome (AMPS) in children ages 8-18. Nerivio® is a wearable device that activates specific nerves in the upper arm. This causes a response from the brain that has been helpful for people who ex...

What is the current status of trial NCT07249931?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2025-12-01. Estimated completion is 2028-12-31.

What interventions are being tested in trial NCT07249931?

The interventions under investigation include: Usual Care (OTHER), Nerivio(R) Device (DEVICE).

Who is sponsoring clinical trial NCT07249931?

This trial is sponsored by Children's Health, which has 4 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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