RECRUITING

Community Testing of Wearable Assistance

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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

This feasibility study looks to evaluate ankle exoskeleton assistance in community settings for individuals with cerebral palsy.

Official Title

Community Testing of Wearable Assistance

Quick Facts

Study Start:2023-10-25

Study Completion:2025-09-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06244901

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:12 Years to 45 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD, ADULT

Inclusion Criteria	Exclusion Criteria
* Diagnosis of cerebral palsy * Gross Motor Function Classification Level I, II, or III * Able to walk for at least 20 minutes with or without a walking aid * Able to safely fit into a device configuration and tolerate assistance without knee hyperextension while walking * Able to provide verbal assent, if appropriate. If the participant is non-verbal, parental interpretation of gesticulation for assent will be used.	* Any neurological, musculoskeletal or cardiorespiratory injury, health condition ( including pregnancy), or diagnosis other than cerebral palsy that would affect the ability to walk as directed for short periods of time. * Participant or parent report that the perspective participant's physician has recommended that they not engage in moderate intensity walking exercise.

Inclusion Criteria

Exclusion Criteria

* Diagnosis of cerebral palsy
* Gross Motor Function Classification Level I, II, or III
* Able to walk for at least 20 minutes with or without a walking aid
* Able to safely fit into a device configuration and tolerate assistance without knee hyperextension while walking
* Able to provide verbal assent, if appropriate. If the participant is non-verbal, parental interpretation of gesticulation for assent will be used.

* Any neurological, musculoskeletal or cardiorespiratory injury, health condition ( including pregnancy), or diagnosis other than cerebral palsy that would affect the ability to walk as directed for short periods of time.
* Participant or parent report that the perspective participant's physician has recommended that they not engage in moderate intensity walking exercise.

Contacts and Locations

Study Contact

Zach Lerner, PhD

CONTACT

928-523-1787

Zachary.Lerner@nau.edu

Study Locations (Sites)

Northern Arizona University

Flagstaff, Arizona, 86011

United States

Collaborators and Investigators

Sponsor: Northern Arizona University

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 Date2023-10-25

Study Completion Date2025-09-01

Study Record Updates

Study Start Date2023-10-25

Study Completion Date2025-09-01

Terms related to this study

Additional Relevant MeSH Terms

Cerebral Palsy