Completed

NCT Number: NCT06840366

Motor Rehabilitation and Physical, Mental and Cognitive Health in Patients With Stroke

This study analyzes the effectiveness of a motor rehabilitation program in the functional recovery of stroke patients and its impact physiotherapy, occupational therapy, and neuropsychology are used to measure improvements in balance, mobility, independence in daily activities, and cognitive functions. The intervention involves the use of the Lokomat, a technologically advanced robot-assisted gait training device. Patients are supported in a harness on a treadmill while the robotic system guides their legs through a natural gait cycle. The results will help clarify the relationship between motor recovery and overall well-being, providing evidence to optimize therapeutic strategies for stroke patients.

Completed

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Key information

Conditions

ACV

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Agustín Aibar Almazán

Jaén, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Confirmed diagnosis of ischemic or hemorrhagic stroke.
Age equal to or greater than 18 years.
Patients in the subacute or chronic phase of stroke (≥ 3 months since the event).
Ability to participate in a motor rehabilitation program.
Absence of advanced neurodegenerative diseases that may interfere with the evaluation of results.
Ability to understand and follow basic instructions of the rehabilitation program.
Informed consent signed by the patient or his/her legal representative.

Exclusion criteria

People under 60 years of age.
Presence of serious comorbidities that prevent physical activity or rehabilitation (e.g. severe heart failure, advanced chronic obstructive pulmonary disease).
Patients with severe cognitive impairments that make it difficult to follow the program (e.g. advanced dementia).
Use of drugs that significantly affect motor and cognitive function, interfering with the evaluation of rehabilitation.
Presence of active infections or unstable medical conditions requiring hospitalization.
History of another neurological disorder that may affect functional recovery (e.g. Parkinson's disease, multiple sclerosis).
Participation in another rehabilitation program at the same time, which may interfere with the results of the study.

Treatment and study plan

Lokomat intervention

Other

The intervention will consist of an 8-week motor rehabilitation program, with 3 weekly sessions of 60 minutes each. In the first weeks, joint mobilization and postural control in a sitting position will be worked on, followed by muscle strengthening and balance re-education in a standing position. Subsequently, coordination exercises and assisted walking on different surfaces will be incorporated. In the final phase, independent walking and the integration of functional movements in daily life activities will be encouraged. The program will be adapted to the individual needs of each patient to optimize recovery and improve quality of life.

Primary outcomes

Balance

Time frame: Up to twelve weeks

The Berg Scale is a widely used tool for assessing static and dynamic balance in adults with neuromotor impairments. It consists of 14 items that assess various functional tasks, such as standing, transferring, trunk rotation, and turning gait. Each item is scored on an ordinal scale from 0 to 4, with 0 indicating the lowest functional capacity and 4 indicating independent and safe performance of the task, with a maximum total score of 56 points. Scores below 45 are associated with an increased risk of falls. This scale has demonstrated high interobserver reliability (ICC > 0.95) and concurrent validity in stroke patients.
Postural Control

Time frame: Up to twelve weeks

The Postural Assessment Scale for Stroke Patients (PASS) is specifically designed to assess postural control in stroke patients, both in the acute and chronic phases. It includes 12 items that assess postural maintenance and changes in different positions (recumbent, sitting, and standing). Each item is scored from 0 to 3, with a maximum total score of 36 points. The PASS is particularly sensitive for detecting small functional changes during the early stages of post-stroke recovery and has demonstrated good discriminative and predictive validity for the evolution of postural control and gait. Its use is recom-mended for monitoring clinical progress in the rehabilitation setting.
Functional Independence

Time frame: Up to twelve weeks

The Barthel Index is a commonly used instrument for measuring functional inde-pendence in basic activities of daily living (BADL). It assesses a patient's ability to perform 10 activities, including feeding, dressing, toileting, mobility, and climbing and descending stairs, among others. Scoring varies by task, with a maximum of 100 points awarded, with higher scores indicating greater autonomy. The BI is sensitive to clinical changes after rehabilitation interventions and has high reliability (α > 0.90). It is widely used in clinical research with neurological populations, including post-stroke patients.

Sponsors and collaborators

Lead sponsor

University of Jaén

Other

Registry information

Official study title

Effectiveness of a Motor Rehabilitation Program and Its Impact on Functional Recovery, Mental and Cognitive Health in Patients With Stroke

Important dates

Study start: 2025
Primary completion: 2025
Study completion: 2025
First posted: Feb 21, 2025
Registry last updated: Aug 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.