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NCT06656754 · ClinicalTrials.gov registry record · Early Phase 1

R01.Aim 2.Study 1: IsoReach

A Early Phase 1 study of Stroke, sponsored by Shirley Ryan AbilityLab.

Recruiting
Registry status
Early Phase 1
Development phase
56
Enrollment target
1
Study location

NCT06656754: Recruiting Early Phase 1 study of Stroke, sponsored by Shirley Ryan AbilityLab.

NCT06656754 is a Early Phase 1 study of Stroke that is actively recruiting participants, run by Shirley Ryan AbilityLab. The registered enrollment target is 56 participants, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06656754, a Early Phase 1 study of Stroke, is actively recruiting participants, sponsored by Shirley Ryan AbilityLab.

RECRUITING
Registry status
Early Phase 1
Development phase
56 participants
Enrollment target
1
Study location

Study Summary

To determine the effects of 3D isometric movement training in healthy participants and impaired participants due to a stroke.

Primary Outcome

Maximum distance between the ideal reaching trajectory and the actual trajectory made in unconstrained and constrained movement conditions

Conditions Studied

Interventions

  • OTHER Isometric Reaching

Study Locations (1)

Illinois

  • Shirley Ryan AbilityLab - Chicago

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2024-11-17
Est. Completion 2029-05-01
Phase Early Phase 1
Shirley Ryan AbilityLab

138 total trials

What NCT06656754 shows while recruiting

NCT06656754 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower).

The record links to 1 condition, with Stroke appearing as the primary indexed condition, and to 1 intervention - of which Isometric Reaching is the first listed.

NCT06656754 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT06656754 about?

NCT06656754 is a clinical study titled "R01.Aim 2.Study 1: IsoReach". To determine the effects of 3D isometric movement training in healthy participants and impaired participants due to a stroke.

What is the current status of trial NCT06656754?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 56 participants. The study started on 2024-11-17. Estimated completion is 2029-05-01.

What conditions does trial NCT06656754 study?

This clinical trial studies the following conditions: Stroke.

What interventions are being tested in trial NCT06656754?

The interventions under investigation include: Isometric Reaching (OTHER).

Who is sponsoring clinical trial NCT06656754?

This trial is sponsored by Shirley Ryan AbilityLab, which has 138 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06656754 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Stroke

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06656754's enrollment target sits among peer trials

56 220th of 454 higher than 231 of 454 other Stroke trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Stroke trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06656754, the US trial registry maintained by the National Library of Medicine. NCT06656754 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.