RECRUITING

A Smartphone Application for Neurology and Telemedicine

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 observational research study is designed to assess the feasibility of developing a new software application that can be used in the home using a commercially available camera to measure abnormal body movements associated with Parkinson's disease (PD). The goal of this study is to validate the motor outcomes derived from a consumer camera observing a sub-set of standardized assessment tasks with respect to the reference motion capture system.

Official Title

NeuroVision™: A Smartphone Application for Neurology and Telemedicine

Quick Facts

Study Start:2023-05-11
Study Completion:2025-09-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06245174

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:35 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Male or Female;
  2. * 35 years of age or older;
  3. * Physician-diagnosed Parkinson's disease or other movement disorder such as Essential Tremor or Dystonia;
  4. * One or more mild to moderate motor symptoms of PD (tremor, bradykinesia, akinesia, Parkinsonian gait);
  5. * Hohn and Yahr (Stage I-III);
  6. * Independent ambulator - walker or cane allowed;
  7. * Referring neurologist indicates that prospective subject is not at high fall risk and can safely participate in the study;
  8. * Have participated in prior telehealth visits using videoconferencing app;
  9. * Have used a smartphone in past to record videos;
  10. * Able to provide his/her written informed consent to participate in the study as stated in the informed consent document;
  11. * American-English speaking; able to follow directions in English;
  12. * Normal hearing.
  1. * Inability to understand spoken English or follow simple instructions;
  2. * Inability to provide written informed consent.

Contacts and Locations

Study Contact

Bhawna Shiwani, MS
CONTACT
(508)545-8217
bshiwani@altecresearch.com
Serge Roy, ScD, PT
CONTACT
(508)545-8235
sroy@delsys.com

Principal Investigator

Bhawna Shiwani, MS
PRINCIPAL_INVESTIGATOR
Senior Research Scientist

Study Locations (Sites)

Altec Inc.
Natick, Massachusetts, 01760
United States

Collaborators and Investigators

Sponsor: Altec Inc.

  • Bhawna Shiwani, MS, PRINCIPAL_INVESTIGATOR, Senior Research Scientist

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 Date2023-05-11
Study Completion Date2025-09-30

Study Record Updates

Study Start Date2023-05-11
Study Completion Date2025-09-30

Terms related to this study

Keywords Provided by Researchers

  • Movement Disorders
  • Parkinson's Disease
  • 3D Camera
  • Smartphone
  • Motor Assessment
  • Telehealth

Additional Relevant MeSH Terms

  • Parkinson Disease(PD)