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Post-stroke Gait Rehabilitation Using the SHAJA-R Exoskeleton

NCT07035730 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2025-08-19

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the safety, reliability, and short-term effectiveness of SHAJA-based training in improving walking velocity and endurance in post-stroke patients.

The main questions it aims to answer are:

* Does the SHAJA-based training improve walking velocity and endurance in post-stroke patients compared to conventional gait training?
* Is the SHAJA exoskeleton safe and reliable?

Researchers will compare the SHAJA-based training to a conventional gait training to see if the former works to improve walking ability.

Participants will:

* Perform six SHAJA-assisted gait training sessions or six conventional gait training sessions
* Perform five assessment sessions

Conditions

Interventions

DEVICE

Unilateral hip exoskeleton

Unilateral hip exoskeleton assisted gait training. Gait training will consist of overground walking with the exoskeleton SHAJA for 30-40 minutes.

BEHAVIORAL

Conventional gait training

Conventional gait training will consist of overground walking without the exoskeleton SHAJA for 30-40 minutes.

Sponsors & Collaborators

  • Scuola Superiore Sant'Anna di Pisa

    collaborator OTHER

  • Centro Riabilitativo Villa Beretta

    collaborator UNKNOWN

  • Azienda Ospedaliero, Universitaria Pisana

    collaborator OTHER

  • Carmelo Chisari

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-07
Primary Completion
2026-12-31
Completion
2026-12-31

Countries

  • Italy

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 NCT07035730 on ClinicalTrials.gov