RECRUITING

Error-enhanced Learning & Recovery in 2 & 3 Dimensions

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 study is being done to see how errors lead to improvement. Specifically, we are evaluating the errors stroke participants make during an upper extremity exercise program when reaching for a target using their affected arm. Once we understand the participant's reaching errors, we plan to create a customized reaching exercise according to the individual's specific error tendencies which will lead to better performance on movement ability after training.

Official Title

Error-enhanced Learning & Recovery in 2 & 3 Dimensions

Quick Facts

Study Start:2023-03-01
Study Completion:2025-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05180786

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 CriteriaExclusion Criteria
  1. 1. 18 years of age or older
  2. 2. Chronic stroke (8+ months post stroke event) with primary motor cortex involvement
  3. 3. Hemiparesis
  4. 4. Some degree of both shoulder and elbow movement capability
  1. 1. Bilateral paresis
  2. 2. Severe tactile deficits using the Two-Point Discrimination Test (participant must detect\<11mm)
  3. 3. Severe proprioceptive deficits
  4. 4. Severe spasticity (Modified Ashworth \>3) preventing movement
  5. 5. Aphasia, cognitive impairment, or affective dysfunction that would influence the ability to perform the experiment
  6. 6. Visual deficits, and hemispatial neglect that would prevent the subjects from seeing the targets.
  7. 7. Inability to provide an informed consent
  8. 8. severe current medical problems
  9. 9. diffuse/multiple lesion sites or multiple stroke events
  10. 10. Inability to attain and maintain testing positions
  11. 11. Botox injection to the affected upper extremity within the previous 4 months
  12. 12. Concurrent participation in upper extremity rehabilitation either as part of a research intervention protocol or a prescribed therapy
  13. 13. Participation in previous, similar robotics intervention study
  14. 14. Other neurological issues
  15. * Adults unable to consent
  16. * Individuals who are not yet adults (infants, children, teenagers)
  17. * Pregnant women
  18. * Prisoners
  19. * Vulnerable Populations

Contacts and Locations

Study Contact

Courtney Celian
CONTACT
3122381560
ccelian@sralab.org
Naveed Aghamohammadi
CONTACT
7654215544
nagham2@uic.edu

Principal Investigator

James Patton, PhD
PRINCIPAL_INVESTIGATOR
Shirley Ryan AbilityLab

Study Locations (Sites)

Shirley Ryan AbilityLab (Healthy Participants)
Chicago, Illinois, 60611
United States
Shirley Ryan AbilityLab
Chicago, Illinois, 60611
United States
Shirley Ryan AbilityLab
Chicago, Illinois, 60611
United States

Collaborators and Investigators

Sponsor: Shirley Ryan AbilityLab

  • James Patton, 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 Date2023-03-01
Study Completion Date2025-12-30

Study Record Updates

Study Start Date2023-03-01
Study Completion Date2025-12-30

Terms related to this study

Keywords Provided by Researchers

  • Upper Extremity
  • Rehabilitation
  • Arm
  • Robotics
  • Stroke

Additional Relevant MeSH Terms

  • Stroke
  • Cerebral Vascular Accident (CVA)/Stroke