RECRUITING

Intuitive Control of a Hybrid Prosthetic Leg During Ambulation

Conditions

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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 objective of this research is to determine the clinical benefits of an innovative and lightweight powered leg controlled using our intent recognition framework in laboratory and community environments.

Official Title

Intuitive Control of a Hybrid Prosthetic Leg During Ambulation

Quick Facts

Study Start:2018-12-01

Study Completion:2025-06-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT04038151

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 95 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* A unilateral or bilateral lower limb amputation * K2/K3/K4 ambulator with a prosthesis * English speaking	* Significant new injury that would prevent use of a prosthesis: The ability to consistently wear a prosthesis and perform activities of daily living and specific performance tasks is necessary to evaluate the relative benefits of the interventions. * Cognitive impairment sufficient to adversely affect understanding of or compliance with study requirements, ability to communicate experiences, or ability to give informed consent: The ability to understand and comply with requirements of the study is essential in order for the study to generate useable, reliable data. The ability to obtain relevant user feedback through questionnaires and informal discussion adds significant value to this study. * Significant other comorbidity: Any other medical issues or injuries that would preclude completion of the study, use of the prostheses, or that would otherwise prevent acquisition of useable data by researchers.

Inclusion Criteria

Exclusion Criteria

* A unilateral or bilateral lower limb amputation
* K2/K3/K4 ambulator with a prosthesis
* English speaking

* Significant new injury that would prevent use of a prosthesis: The ability to consistently wear a prosthesis and perform activities of daily living and specific performance tasks is necessary to evaluate the relative benefits of the interventions.
* Cognitive impairment sufficient to adversely affect understanding of or compliance with study requirements, ability to communicate experiences, or ability to give informed consent: The ability to understand and comply with requirements of the study is essential in order for the study to generate useable, reliable data. The ability to obtain relevant user feedback through questionnaires and informal discussion adds significant value to this study.
* Significant other comorbidity: Any other medical issues or injuries that would preclude completion of the study, use of the prostheses, or that would otherwise prevent acquisition of useable data by researchers.

Contacts and Locations

Study Contact

Suzanne Finucane

CONTACT

312-238-0937

sfinucane@sralab.org

Principal Investigator

Levi Hargrove, PhD

PRINCIPAL_INVESTIGATOR

Shirley Ryan AbilityLab

Study Locations (Sites)

Shirley Ryan AbilityLab

Chicago, Illinois, 60611

United States

Collaborators and Investigators

Sponsor: Shirley Ryan AbilityLab

Levi Hargrove, PhD, PRINCIPAL_INVESTIGATOR, Shirley Ryan AbilityLab

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 Date2018-12-01

Study Completion Date2025-06-30

Study Record Updates

Study Start Date2018-12-01

Study Completion Date2025-06-30

Terms related to this study

Keywords Provided by Researchers

Transfemoral Amputation

Additional Relevant MeSH Terms

Amputation