NCT07698522

Brief Summary

The goal of this study is to determine the effects of lab and home-based technology guidance during movement training post-stroke. The study will compare movement training informed by lab-based technology to training delivered with technology at home. The main questions it aims to answer are:

  • How well do lab and home-based technologies help individuals post-stroke improve their movement patterns?
  • Is there a difference in improvement between the in-lab and at-home training groups?
  • Which technologies lead to the most improvement?

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P50-P75 for not_applicable stroke

Timeline
89mo left

Started Jul 2026

Longer than P75 for not_applicable stroke

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress1%
Jul 2026Dec 2033

Study Start

First participant enrolled

July 1, 2026

Completed
5 days until next milestone

First Submitted

Initial submission to the registry

July 6, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 13, 2026

Completed
7.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2033

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2033

Last Updated

July 20, 2026

Status Verified

July 1, 2026

Enrollment Period

7.4 years

First QC Date

July 6, 2026

Last Update Submit

July 17, 2026

Conditions

Stroke

Keywords

movement trainingrehabilitationoccupational therapy

Outcome Measures

Primary Outcomes (1)

  • Kinematic movement quality score

    A score based on subject kinematics during a daily task (like reaching), comparing the subject's reaching kinematics to normative kinematics.

    From enrollment to the end of treatment at 3 weeks.

Secondary Outcomes (1)

  • FMA-UE Score

    From enrollment to the end of treatment at 3 weeks.

Study Arms (2)

At-Home Training

EXPERIMENTAL

Participants will train at-home.

Other: Home-based movement guidance

In-Lab Training

EXPERIMENTAL

Participants will train in the lab.

Other: Lab-based movement guidance

Interventions

Lab-based movement guidanceOTHER

Participants will receive computer-generated guidance on how to perform different activities of daily living efficiently. The guidance will be delivered using lab-based sensing and feedback technology.

In-Lab Training
Home-based movement guidanceOTHER

Participants will receive computer-generated guidance on how to perform different activities of daily living efficiently. This guidance will be delivered using home-based technologies, such as a computer or tablet.

At-Home Training

Eligibility Criteria

Age30 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age between 30-85 years.
  • Diagnosis of stroke.
  • Stroke onset of at least six months prior to the time of participation.
  • Fugl Meyer Upper Extremity between 30-50 (mild-moderate)
  • Cognitive skills to consent and actively participate, as indicated by scores of ≥ 24 on the Mini- Mental Status Examination
  • Able to visit lab up to 5x per week for 3 weeks

You may not qualify if:

  • Presence of severe aphasia preventing the ability to follow 1-step directions at least 80% of the time.
  • Excessive spasticity of the wrist, elbow, and shoulder, defined as a Modified Ashworth Score \>2.
  • Diagnosis of neurological disorders other than stroke.
  • Orthopedic/musculoskeletal conditions (e.g., severe arthritis) affecting the upper extremity.
  • Currently or planning to become pregnant.
  • Participation in concurrent occupational therapy.
  • Unilateral neglect, defined as failure of the Line Bisection Task
  • Upper extremity pain \>= 7/10 on Numeric Rating Scale

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kennecott Mechanical Engineering Building

Salt Lake City, Utah, 84112, United States

RECRUITING

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Scott Uhlrich, PhD

    University of Utah

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Samantha McNeill

CONTACT

(385) 215-9146‬samantha.mcneill@utah.edu

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 6, 2026

First Posted

July 13, 2026

Study Start

July 1, 2026

Primary Completion (Estimated)

December 1, 2033

Study Completion (Estimated)

December 1, 2033

Last Updated

July 20, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will share

We will share participant demographics and outcomes data. We will also share kinematics data. These data will be shared on SimTK.org.

Shared Documents
ANALYTIC CODE
Time Frame
Code and data will be shared upon publication.
Access Criteria
Code and data will be shared publicly on SimTK.org.

Locations

US(1)