RECRUITING

A Room Temperature Atomic Magnetrode System for Telemetry of Epileptic Seizures

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study is being done to help scientists learn about the use of a device called an atomic magnetometer. The device uses sensors called optically-pumped magnetometers (OPM) which function at room temperature. This research will compare the non-invasive brain imaging application of the OPM sensors to the present SQUID-based cryogenic sensor technique used in conventional Magnetoencephalography (MEG). This study is being conducted in conjunction with the University of Colorado Boulder's Mechanical Engineering Department.

Official Title

Development of A Room Temperature Atomic Magnetrode System for Telemetry of Epileptic Seizures

Quick Facts

Study Start:2021-03-01
Study Completion:2025-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04515316

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Project A: Any adult subject, who is at least eighteen (18 - 70) years old.
  2. * Project B: Any clinical patient referred to us via the clinical MEG program, and who is at least eighteen (18 - 70) years old.
  1. * ONLY applicable to Project A: have a history of neurological disorders (e.g., epilepsy, Parkinson disease, Alzheimer's disease, Autism, etc...).
  2. * BOTH projects: have large amounts of metal or other magnetic field producing components present in their body or external to their body close to the measurement site, which are needed for normal functioning (e.g., metal implants, pacemakers, hearing aids, braces etc.). There is no harm to the subject with metal, it disturbs the sensor reading. Dental fillings are not excluded.
  3. * BOTH projects: pregnant women.
  4. * ONLY applicable to Project A: are not comfortable lying still for the time of the recording.
  5. * BOTH projects: are unable to offer independent informed consent to study participation.

Contacts and Locations

Study Contact

Isabelle Buard, PhD
CONTACT
303-724-5973
Isabelle.Buard@CUAnschutz.edu
Lucas Lattanzio, BA
CONTACT
303-724-2205
Lucas.Lattanzio@CUAnschutz.edu

Study Locations (Sites)

University of Colorado School of Medicine - Anschutz Medical Campus
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-03-01
Study Completion Date2025-12-31

Study Record Updates

Study Start Date2021-03-01
Study Completion Date2025-12-31

Terms related to this study

Keywords Provided by Researchers

  • epilepsy
  • MEG

Additional Relevant MeSH Terms

  • Epilepsy