ACTIVE_NOT_RECRUITING

A Multi-Modal Remote Monitoring Platform for Frontotemporal Lobar Degeneration (FTLD) Syndromes

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

The primary objective of this study is to enroll an observational cohort of approximately 60 patients with PSP over the course of 24 months using a multicenter study design and to follow each of them for 12 months. The secondary objective of this study is to develop a robust solution for multi-modal remote monitoring of motor symptoms and function in PSP that can be applied to other Frontotemporal lobar degeneration (FTLD) syndromes.

Official Title

A Multi-Modal Remote Monitoring Platform for Frontotemporal Lobar Degeneration (FTLD) Syndromes

Quick Facts

Study Start:2023-07-28
Study Completion:2027-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05956834

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:40 Years to 89 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Clinical diagnosis of possible or probable PSP as defined by the 2017 MDS criteria
  2. * Fluent in reading and speaking English and capable of providing informed consent based on the principal investigator's judgement
  3. * Able to walk 10 feet unassisted at the time of initial enrollment
  4. * Must have a caregiver or study partner who is willing and able to assist with all study-related procedures
  1. * Any neurological, medical, or psychiatric condition that would preclude participation in study activities based on the investigator's judgment.
  2. * A history of frequent falls defined as more than 5 falls per month, or who require a walker to ambulate safely at baseline will not be eligible to participate in the study.

Contacts and Locations

Study Locations (Sites)

Johns Hopkins School of Medicine
Baltimore, Maryland, 21093
United States
Massachusetts General Hospital
Boston, Massachusetts, 02114
United States

Collaborators and Investigators

Sponsor: Massachusetts General Hospital

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 Date2023-07-28
Study Completion Date2027-12-30

Study Record Updates

Study Start Date2023-07-28
Study Completion Date2027-12-30

Terms related to this study

Additional Relevant MeSH Terms

  • PSP
  • CBD
  • Progressive Supranuclear Palsy
  • FTD
  • Corticobasal Degeneration
  • Frontotemporal Dementia
  • Frontotemporal Lobar Degeneration