RECRUITING

Analysis of Human Movement With Assistive Devices

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 research is to evaluate how people move about in different settings with different assistive devices or components, and to understand how people interact with different assistive technologies. Individuals that have limb weakness, limb paralysis, limb loss, and movement disorders are often provided assistive devices such as prostheses and orthoses to assist with mobility or use assistive technologies for purposes such as to regain muscle strength or retrain movements. It is important to understand the impact of these different assistive technologies on human movement for technology improvement and in preparation for commercialization. Because this research focuses on evaluating how different people move about in different settings with different assistive devices/components, there are different activities that may take place. These activities have been classified as (1) Movement Analysis in the Laboratory, (2) Movement Analysis Outside the Laboratory, (3) Usability Testing, and (4) Focus Groups. Each participant may or may not complete the same activities as the other participants. Each participant may or may not complete all of the activities. Participants may complete the activities more than once.

Official Title

Analysis of Human Movement With Assistive Devices

Quick Facts

Study Start:2022-11-28
Study Completion:2024-11-28
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05729061

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 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Adam Arabian, PhD
CONTACT
425-771-0797
arabian@orthocareinnovations.com

Principal Investigator

Adam Arabian, PhD
PRINCIPAL_INVESTIGATOR
Orthocare Innovations, LLC

Study Locations (Sites)

Orthocare Innovations, LLC
Edmonds, Washington, 98020
United States

Collaborators and Investigators

Sponsor: Orthocare Innovations, LLC

  • Adam Arabian, PhD, PRINCIPAL_INVESTIGATOR, Orthocare Innovations, 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 Date2022-11-28
Study Completion Date2024-11-28

Study Record Updates

Study Start Date2022-11-28
Study Completion Date2024-11-28

Terms related to this study

Additional Relevant MeSH Terms

  • Limb Loss
  • Limb Weakness
  • Limb Paralysis
  • Movement Disorders