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CompletedNCT06180577Updated Nov 22, 2024

A Survey Study to Assess the Accessibility of the Nerivio Device At School

An observational study in Migraine in Children, sponsored by Theranica. Completed at 1 site in United States. Open to participants aged Up to 18 Years. Per ClinicalTrials.gov, last updated 2024-11-22.

Sponsored by Theranica · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
332
Ages
Up to 18 Years
Sex
All
01

Study summary

This is a retrospective survey-study to assess the accessibility, preference, and frequency of adolescents using Nerivio by itself, in combination with pharmacological medications, or not at all, in the school setting. The study population is prescribed Nerivio users, under the age of 18 years old, who have used the Nerivio device at least once. The study will be conducted electronically, and will include eligibility questions, an electronic informed consent form signed by the parent/legal guardian (e-ICF), an assent form signed by the adolescent patient (e-Assent), and an e-survey relating to the management of headaches due to migraine attacks. Participants will be recruited from Nerivio's userbase and will be compensated for their participation.

Read the detailed description

This is a retrospective survey-study to assess the accessibility, preference, and frequency of adolescents using Nerivio by itself, in combination with pharmacological medications, or not at all, in the school setting. The study population is prescribed Nerivio users, under the age of 18 years old, who have used the Nerivio device at least once.

Study group: Participants will be recruited from Nerivio's user database. An invitation message will be sent via emails and/or in-app notifications to Nerivio users who are (1) under the age of 18 years old, and (2) treated with Nerivio at least once. Adolescents who meet these criteria will be invited to answer a screening questionnaire verifying eligibility.

Adolescents who are found eligible will be offered the opportunity to participate in the study. If they are willing, they will first be directed to an Informed Consent Form (e-ICF) to be signed by the participant's parent/legal guardian. A copy of the completed form will be automatically sent to the parent/legal guardian upon completion. If the parent/legal guardian consents via the e-ICF to his/her child's participation, an electronic assent form will follow and must be signed by the adolescent patient. A copy of the assent form will be automatically sent to the parents and the adolescent patient. Once both electronic consent forms are signed, the adolescent patient will be enrolled in the study and will be directed to the study survey.

Primary outcome measures:

Percent of adolescents' who prefer treating headaches due to migraine when they are at school with Nerivio alone, relative to other options (combination, pharmaceutical, not treating while in school).

Secondary outcome measures:

    • Distribution of barriers to adolescents who report the necessity to treat their headaches due to migraine while at school, including the need to leave class for treatment, lack of availability of treatments while at school, and time delay to treat headaches.
    • Distribution of treatments used by adolescents at school to treat migraine headaches prior to being prescribed Nerivio (specific pharmaceutical agents, or not treating at all) reflecting convergence to using Nerivio at school.
02

Conditions studied

  • Migraine in Children

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Keywords

  • Migraine
  • Nerivio
  • Headache
03

In context

Migraine Disorders

1,528 studies on the registry are indexed under Migraine Disorders; 299 are open to participants now.

This study's enrollment of 332 is above the median of 130 across 299 observational studies indexed under Migraine Disorders.

Browse Migraine Disorders studies →

Lead sponsor

Theranica is the lead sponsor of 27 studies on the registry; 3 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 6 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Adolescents with migraine who used Nerivio at least once

Inclusion criteria

  • Age ≤18 years old at registration to the Nerivio app
  • Treated with Nerivio at least once (≥30 minutes/treatment).
  • Attended elementary, middle, junior high, or high school, while first prescribed Nerivio
  • Must obtain parent/legal guardian consent form prior to signing the assent form by the adolescent and engaging in study survey.

Exclusion criteria

Exclusion Criteria:

  • None
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
332 participants (actual)
Patient registry
No

Groups and cohorts

  • Adolescent Nerivio Users

    Adolescent with migraine who used Nerivio at least once

    Device: Nerivio

Interventions

  • DeviceNerivio

    Nerivio is a prescribed Remote Electrical Neuromodulation (REN) device for treatment of migraine

06

What researchers measure

Primary outcomes

  1. Nerivio usage at school

    Percent of adolescents who prefer treating headaches due to migraine when they are at school with Nerivio alone, relative to other options (combination, pharmaceutical, not treating while in school).

    Time frame: 1 year

Secondary outcomes

  1. Limitations to migraine treatment at school

    Distribution of barriers to adolescents who report the necessity to treat their headaches due to migraine while at school, including need to leave class for treatment, lack of availability of treatments while at school, time delay to treat headaches.

    Time frame: 1 year

  2. Types of migraine treatments during school

    Distribution of treatments used by adolescents at school to treat migraine headaches prior to being prescribed Nerivio (specific pharmaceutical agents, or not treating at all) reflecting convergence to using Nerivio at school.

    Time frame: 1 year

07

Study locations

1 site
  • Theranica USA Inc
    Bridgewater, New Jersey 08807, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 22, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06180577
Lead sponsor
Theranica
Responsible party
Sponsor
First posted
Dec 22, 2023
Start date
Feb 1, 2024
Primary completion
May 1, 2024
Completion
May 15, 2024
Last update
Nov 22, 2024

Study contacts

Alit Stark Inbar, PhD
study director · Theranica Bio-Electronics Ltd

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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