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StrokeNCT06748378

Gait Parameters After Using the Tilt-table Exercise and Motor Imagery.

A study testing Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait. and Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters. in people with Stroke and Visualization, run by Anna Olczak at 1 site in Poland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Sixty-six stroke patients were randomly assigned to three groups (conventional, with the addition of the Erigo®Pro table, and enriched with motor imagery). The Trunk Stability Test, walking speed, step symmetry, and lower limb load symmetry on the Riablo device, as well as the superficial tension of the transverse… Read more about this study

Who is it for?
Ages 30 to 85 years
Conditions the study is for
Stroke, Visualization, Gait Analysis
What is being tested?
Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait. and Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters.
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
66 participants
Where
1 sitePoland
Study dates
1 Dec 2024to 15 Aug 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 30 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 1) patients 6-8 weeks post-stroke,
  • 2) aged 38-85 years, mean,
  • 3) males and females,
  • 4) walking with or without assistance (modified Rankin scale = 3),
  • 5) with slight neurological deficits (NIHSS ≤7).

Who cannot join

  • 1) stroke up to six weeks after the episode,
  • 2) epilepsy,
  • 3) no possibility to sit and stand,
  • 4) persistent deficit of speech and cognitive functions, lack of attention,
  • 5) visual disturbances,
  • 6) depression,
  • 7) high or very low blood pressure, dizziness, malaise.

Trial locations and contacts

1 site in 1 country.

Poland1 site
  • Military Institute of Medicine National Research Institute

    Warsaw, Masovian District, 04-141

Other trials in Poland

About this study

Official title: Analysis of Gait Parameters After Therapy Using the Tilt-table Exercise and Motor Imagery - a Randomized Observational Study on Stroke Patients.

Sixty-six stroke patients were randomly assigned to three groups (conventional, with the addition of the Erigo®Pro table, and enriched with motor imagery). The Trunk Stability Test, walking speed, step symmetry, and lower limb load symmetry on the Riablo device, as well as the superficial tension of the transverse abdominis and multifidus muscles, were assessed before and after completing therapy.

Read the detailed description

Sixty-six stroke patients were randomly assigned to three groups (conventional, with the addition of the Erigo®Pro table, and enriched with motor imagery). The Trunk Stability Test, walking speed, step symmetry, and lower limb load symmetry on the Riablo device, as well as the superficial tension of the transverse abdominis and multifidus muscles, were assessed before and after completing therapy.

Results: In each of the groups studied, the therapies used significantly improved the functional assessment of trunk stability (Trunk Control Test <0.001)). Additionally, after the intervention, the Erigo group showed a greater gait speed (p=0.003), while the Visualization group exhibited a higher level of tension in the multifidus (p=0.011) and transverse abdominal muscles (p=0.002).

Being tested
Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait., Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters.
Keywords
gait analysis, Erigo Pro, motor imagery, stroke
Medical subject headings
Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait.Procedure or surgery

    66 stroke patients were randomly assigned to three groups (22 people each) with different therapies (conventional, with the addition of Erigo®Pro and enriched with motor imagery). The therapy duration was two weeks. Patients underwent assessment before and after completion of therapy. The study used the Trunk Stability Test, and the Riablo device to measure gate parameters. Additionally, an evaluation of the superficial tension of the transverse abdominis and multifidus muscles was conducted.

  • Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters.Procedure or surgery

    66 stroke patients were randomly assigned to three groups (22 people each) with different therapies (conventional, with the addition of Erigo®Pro and enriched with motor imagery). The therapy duration was two weeks. Patients underwent assessment before and after completion of therapy. The study used the Trunk Stability Test, and the Riablo device to measure the gate parameters. Additionally, an evaluation of the superficial tension of the transverse abdominis and multifidus muscles was conducted.

Study groups in NCT06748378
Study groupRoleWhat they receive
Conventional rehabilitationExperimentalIn conventional rehabilitation, patients performed daily physiotherapy, which included intensive preparatory training for standing and sitting positions, strengthening exercises, weight-bearing exercises, and balance and coordination exercises (from 40 to 60 minutes of therapy). Interventions: Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery
Receives: Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait.; Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters.
Erigo®ProExperimentalInterventions: Effective therapy included 1 session on a tilting table at an angle of 42° for 20 minutes, 5 times a week (Monday to Friday) at a speed of 32 steps per minute, followed by a physiotherapy session for two weeks. Interventions: Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery
Receives: Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait.; Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters.
motor imagery (MI)Experimentalin addition to conventional physiotherapy, activity imagery during passive walking on the Erigo®Pro table was introduced. During the exercises on the table, the patients wore headphones that blocked out any external sounds, closed their eyes and their task was to imagine the sensation of their body moving (first-person imagination), differentiating the idea of walking in various real environments (park, forest, beach, snow, streets). in the city, walking at different speeds, going up and down stairs, running, etc.). Interventions: Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery
Receives: Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait.; Procedure: Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Trunk Control Test

    Assessment of trunk stability before and after therapy

    Measured: two weeks

Secondary outcomes (2)
  1. RiabloTM device

    Assessment of gate parameters before and after therapy

    Measured: two weeks

  2. Luna EMG

    Assessment of the surface tension of the transverse abdominis muscle and the tension of the multifidus muscle

    Measured: two weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Dec 2024
  2. Study start1 Dec 2024
  3. Primary completion15 Jul 2025
  4. Study completion15 Aug 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Allocation Randomized Interventional Model Parallel Assignment Masking Double (Participant Outcomes Assessor) Primary Purpose Treatment
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
66 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06748378
Sponsor's protocol ID
11/KRN/2020
Status last verified
Dec 2024
First submitted
16 Dec 2024
Last updated
5 Feb 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait. and Conventional rehabilitation, the Erigo®Pro table, motor imagery on gait parameters. in people with Stroke and Visualization, run by Anna Olczak at 1 site in Poland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Trunk Control Test (time frame: two weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Feb 2026.

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