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Integrated Cueing for Stroke Recovery (EOIC Trial)

N/A
Waitlist Available
Led By Eric G Johnson, DSc
Research Sponsored by Loma Linda University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Must be able to stand without an assistive device or ankle foot orthosis
Chronic Right CVA with left hemiplegia > 6 Months
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and immediately after the intervention
Awards & highlights

EOIC Trial Summary

This trial will test whether physical therapists using an integrated verbal and manual facilitation approach can improve movement quality in persons recovering from stroke.

Who is the study for?
This trial is for chronic stroke survivors who've had a right CVA resulting in left hemiplegia for over 6 months. Participants must be able to stand without help or devices and follow verbal commands but can't have other conditions affecting their ability to perform sit-to-stand movements safely.Check my eligibility
What is being tested?
The study tests the immediate and lasting effects of an integrated cueing method by physical therapists, combining verbal and manual cues, on movement quality during sit-to-stand exercises in individuals with hemiplegia from a stroke.See study design
What are the potential side effects?
Since this trial involves physical therapy techniques rather than medications, typical drug side effects are not expected. However, participants may experience fatigue or muscle soreness due to the physical nature of the interventions.

EOIC Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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You can stand without needing help from a device or special brace for your ankle or foot.
Select...
You have had a stroke on the right side of your brain that has caused paralysis on the left side of your body for more than 6 months.
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You can walk with minimal assistance, such as someone watching over you.

EOIC Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and immediately after the intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline and immediately after the intervention for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Midline Orientation via Symmetry Ratio
Midline Orientation via Trunk Lateral Lean angle
Muscle Activation
+1 more

EOIC Trial Design

2Treatment groups
Experimental Treatment
Group I: Verbal Cueing GroupExperimental Treatment1 Intervention
A series of 40 training repetitions of sit to stand using the Verbal Cueing intervention
Group II: Integrated Manual and Verbal Cueing GroupExperimental Treatment1 Intervention
A series of 40 training repetitions of sit to stand using the Integrated/Manual Cueing intervention.

Find a Location

Who is running the clinical trial?

Loma Linda UniversityLead Sponsor
306 Previous Clinical Trials
260,967 Total Patients Enrolled
Eric G Johnson, DScPrincipal InvestigatorLoma Linda University
1 Previous Clinical Trials
50 Total Patients Enrolled

Media Library

Integrated Cueing Protocol Clinical Trial Eligibility Overview. Trial Name: NCT04498429 — N/A
Hemiplegia/Hemiparesis Research Study Groups: Integrated Manual and Verbal Cueing Group, Verbal Cueing Group
Hemiplegia/Hemiparesis Clinical Trial 2023: Integrated Cueing Protocol Highlights & Side Effects. Trial Name: NCT04498429 — N/A
Integrated Cueing Protocol 2023 Treatment Timeline for Medical Study. Trial Name: NCT04498429 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~5 spots leftby Apr 2025