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Acute Effect of Locomotion Training with Visual and Auditory Stimuli on kinematic parameters and locomotion confidence in individuals after Stroke: a randomized clinical trial

Acute effect of biofeedback Gait Training on kinematic parameters and walking confidence in individuals after Stroke: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5qkchbv
Enrollment
Unknown
Registered
2026-01-19
Start date
2025-10-10
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Stroke

Interventions

Participants will be randomized into two groups, each containing 15 participants, totaling a sample of 30 participants. One experimental group will undergo treadmill gait training with visual and audi

Sponsors

Faculdade de Fisioterapia
Lead Sponsor
Universidade Federal de Juiz de Fora
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Both genders; who suffered a stroke less than 6 months ago (acute); who present residual motor impairments in at least one lower limb; aged 18 years or older; ambulate independently without the need for assistive devices; achieve the minimum score on the six-item cognitive impairment test (6CIT-P) for cognitive function assessment (which varies according to education level); muscle tone in the affected lower limb with a score between 1 and 1+ on the Ashworth scale

Exclusion criteria

Exclusion criteria: Patients who do not demonstrate safety to walk on the treadmill even after 3 familiarization sessions; those who experience adverse events during the intervention such as severe pain, falls, excessive fatigue, or any hemodynamic instability that contraindicates the continuation of the protocol; participants should not have bilateral motor impairment, nor an associated diagnosis of other neurological diseases (such as Parkinson's disease or multiple sclerosis), nor severe hearing or visual impairments that hinder the reception of biofeedback stimuli; those currently using botulinum toxin in the lower limbs or with decompensated cardiovascular disorders; during follow-up, participation will be considered irregular if the volunteer attends less than 70% of the sessions scheduled in the protocol. In this situation, the participant will be removed from the study, as low attendance could compromise both the effectiveness of the treatment and the reliability of the results

Design outcomes

Primary

MeasureTime frame
To analyze the acute effect of biofeedback gait training on gait speed, kinematic parameters, and gait confidence in individuals after stroke

Secondary

MeasureTime frame
To examine the effect of the proposed training on the range of hip and knee flexion and its relationship with the patient's confidence when walking

Countries

Brazil

Contacts

Public ContactKethane Lorrayne Silva

Faculdade de Fisioterapia

kethanesantos@gmail.com+55 (32) 999109474

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 7, 2026