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Personal KinetiGraph® Clinical Validation Study

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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

The purpose of this study is to clinically validate new measures of the Personal KinetiGraph® (PKG®).

Official Title

Personal KinetiGraph® Clinical Validation Study

Quick Facts

Study Start:2022-12-09

Study Completion:2025-09-03

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT05251701

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

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Able and willing to sign a written informed consent for study participation * Existing diagnosis of a movement disorder or a healthy control subject without diagnosis of a movement disorder	* Bedridden, wheelchair confined, or requires the regular use of an assistive gait device (e.g., walker, cane, etc.) * Occupation that involves repetitive movement or complete immobility (e.g., janitor, construction, or sedentary with no/limited arm movements such as a taxi driver) * In the investigator's or sponsor's opinion, subject has any unstable or clinically significant condition that would impair the participant's ability to complete the required PKG watch wear (e.g., subject unable to complete PKG wear instructions per Patient Instruction Manual), complete required assessments or interfere with data collection.

Inclusion Criteria

Exclusion Criteria

* Able and willing to sign a written informed consent for study participation
* Existing diagnosis of a movement disorder or a healthy control subject without diagnosis of a movement disorder

* Bedridden, wheelchair confined, or requires the regular use of an assistive gait device (e.g., walker, cane, etc.)
* Occupation that involves repetitive movement or complete immobility (e.g., janitor, construction, or sedentary with no/limited arm movements such as a taxi driver)
* In the investigator's or sponsor's opinion, subject has any unstable or clinically significant condition that would impair the participant's ability to complete the required PKG watch wear (e.g., subject unable to complete PKG wear instructions per Patient Instruction Manual), complete required assessments or interfere with data collection.

Contacts and Locations

Principal Investigator

Zoltan Mari, MD

PRINCIPAL_INVESTIGATOR

Z Neurosciences, LLC.

Study Locations (Sites)

Tucson Neuroscience Research

Tucson, Arizona, 85710

United States

Collaborators and Investigators

Sponsor: Global Kinetics Corporation

Zoltan Mari, MD, PRINCIPAL_INVESTIGATOR, Z Neurosciences, LLC.

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 Date2022-12-09

Study Completion Date2025-09-03

Study Record Updates

Study Start Date2022-12-09

Study Completion Date2025-09-03

Terms related to this study

Additional Relevant MeSH Terms

Movement Disorders
Parkinson Disease