RECRUITING

Clinical Validation of DystoniaNet Deep Learning Platform for Diagnosis of Isolated Dystonia

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Conditions

DystoniaDrug Induced DystoniaParkinson DiseaseEssential TremorDyskinesiasMyoclonusTic DisordersTorticollisUlnar Nerve EntrapmentTemporomandibular Joint DisordersDysphonia

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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 research involves retrospective and prospective studies for clinical validation of a DystoniaNet deep learning platform for the diagnosis of isolated dystonia.

Official Title

Clinical Validation of DystoniaNet Deep Learning Platform for Diagnosis of Isolated Dystonia

Quick Facts

Study Start:2022-06-01
Study Completion:2027-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05317390

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Males and females of diverse racial and ethnic backgrounds, with age across the lifespan;
  2. 2. Patients will have at least one of the forms of dystonia, including focal dystonia (e.g., laryngeal, cervical, oromandibular, blepharospasm, focal hand, musicians), segmental dystonia, or generalized dystonia;
  3. 3. Patients will have other movement disorders (Parkinson's disease, essential tremor, dyskinesia, myoclonus) and other non-neurological conditions (tic disorders, torticollis, ulnar nerve entrapments, temporomandibular disorders, dysphonia) that mimic dystonic symptoms.
  1. 1. Patients who are incapable of giving informed consent;
  2. 2. Patients who are unable to undergo brain MRI due to the presence of certain tattoos and ferromagnetic objects in their bodies (e.g., implanted stimulators, surgical clips, prosthesis, artificial heart valve) that cannot be removed or due to pregnancy or breastfeeding at the time of the study.

Contacts and Locations

Study Contact

Kristina Simonyan, MD, PhD
CONTACT
617-573-6016
simonyan_lab@meei.harvard.edu

Principal Investigator

Kristina Simonyan, MD, PhD
PRINCIPAL_INVESTIGATOR
Massachusetts Eye and Ear

Study Locations (Sites)

Massachusetts Eye and Ear Infirmary
Boston, Massachusetts, 02114
United States

Collaborators and Investigators

Sponsor: Massachusetts Eye and Ear Infirmary

  • Kristina Simonyan, MD, PhD, PRINCIPAL_INVESTIGATOR, Massachusetts Eye and Ear

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 Date2022-06-01
Study Completion Date2027-04-30

Study Record Updates

Study Start Date2022-06-01
Study Completion Date2027-04-30

Terms related to this study

Additional Relevant MeSH Terms

  • Dystonia
  • Drug Induced Dystonia
  • Parkinson Disease
  • Essential Tremor
  • Dyskinesias
  • Myoclonus
  • Tic Disorders
  • Torticollis
  • Ulnar Nerve Entrapment
  • Temporomandibular Joint Disorders
  • Dysphonia