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Repetitive Action Simulation Circuit Training to Reduce Arm Weakness After a Stroke

NCT07772284 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2026-08-19

No results posted yet for this study

Summary

This study aims to examine the effect of an action simulation circuit training for individuals who have experienced upper extremity weakness following a stroke. The study will also examine the feasibility of the intervention as an occupational therapy rehabilitation approach.

Participants will:

* Engage in four workstations within the circuit training format: mental practice, action observation, virtual reality, and repetitive task-specific practice.
* Participate in training 2x/week for 6 weeks (12 sessions).

Conditions

  • Stroke
  • Hemiparesis of the Upper Limb Following Stroke

Interventions

OTHER

Upper Extremity Action Simulation Circuit Training

Participants rotate between four workstations: 1. Mental Practice: participants listen to an audio-guided recording that promotes the cognitive rehearsal of performing a task with their affected upper extremity. 2. Virtual Reality: participants perform virtual reality activities or games involving the use of their upper extremities. 3. Action Observation: participants watch video clips of individuals performing upper extremity tasks. 4. Repetitive-Task Specific Practice: participants physically rehearse various upper extremity tasks with the assistance of an occupational therapist.

Sponsors & Collaborators

  • Towson University

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-17
Primary Completion
2024-12-20
Completion
2024-12-20

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07772284 on ClinicalTrials.gov