Effects of Neuropilates on Rehabilitation Programs for Chronic Stroke

NCT06127485 | Unknown

• 1 other identifier: 3006202326123
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

Introduction: Cerebrovascular damage (stroke) can generate motor or cognitive sequelae, making rehabilitation (such as the Pilates method) necessary to improve autonomy and quality of life. However, there are no studies on the efficacy of the method in the recovery of the upper limb and the improvement of autonomy after stroke. Methods: Randomized double-blind clinical trial with patients with stroke in semi-acute period, randomized into experimental group (EG) (conventional rehabilitation and Pilates) or control group (CG) (conventional rehabilitation). After randomization and initial evaluation, the intervention will begin (2 sessions per week, 3 months). After completion, there will be post-intervention assessment, and another one at 1 month. Intervention: The CG will receive 30 minutes of physical therapy and 30 minutes of occupational therapy. The SG will receive 20 minutes of physiotherapy, 20 minutes of occupational therapy and 20 minutes of Pilates. Assessment instruments: Mean Functional Independence; Functional Range Test; Timed 'Up and Go'; Nine Hole Peg Test; Box and Block Test; Arm, Shoulder and Hand Disabilities Questionnaire; Client Satisfaction Questionnaire.

Conditions

Stroke; Occupational Therapy; Physiotherapy

Outcome Measures

Primary Outcomes (6)

• Functional Independance Measure (FIM)

  an instrument that measures the level of functional independence in activities of daily living. It provides information mainly on motor and cognitive performance by means of 18 items. items. The score ranges from 1 to 7, with a higher score corresponding to a higher level of functional independence. Administration was carried out by means of task observation and interview.

  pre-intervention (baseline); post-intervention (immediately after the intervention) and follow up (one month after the intervention)

• Functional Reach Test

  A test that measures the maximum distance an individual can move their center of gravity to the limits of their base of support. In a relaxed standing position, with feet at hip level, the person is instructed to make a shoulder flexion to 90 degrees and keep the hand extended. The person has to go forward as far as he/she can. The examiner records the final measurement that they manage to shift their center of gravity. Two practice trials and three recorded trials are completed, and the average is the overall mean score. This test is recorded in centimeters.

  pre-intervention (baseline); post-intervention (immediately after the intervention) and follow up (one month after the intervention)

• Timed 'Up and Go' (TUG)

  A test that measures the time it takes a person to get up from a chair, walk a distance of 3 meters, turn, return to the chair and sit down. This test is responsible for exploring balance and walking speed. This test is recorded in seconds

  pre-intervention (baseline); post-intervention (immediately after the intervention) and follow up (one month after the intervention)

• Nine Hole Peg Test

  This test measures fine manual dexterity. This is considered a "gold standard" to evaluate fine manual dexterity. It consists of placing a number of pins on a board with 9 holes and removing them as quickly as possible. This test records the time that the person uses with each upper limb.

  pre-intervention (baseline); post-intervention (immediately after the intervention) and follow up (one month after the intervention)

• Box and Block Test

  Test that measures the gross motor skills of the upper limbs. It consists of a wooden box that is divided into two halves by an axis, and consists of passing from one half to the other as many wooden blocks as possible with each upper limb, for 1 minute. In this test, the number of blocks that the person is able to pass in one minute with each upper limb is recorded.

  pre-intervention (baseline); post-intervention (immediately after the intervention) and follow up (one month after the intervention)

• Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH)

  This test measures symptoms and some aspects of activity and participation according to the 9 domains described in the International Classification of Functioning, Disability and Health in the upper extremity. It is an easy and quick test to administer

  pre-intervention (baseline); post-intervention (immediately after the intervention) and follow up (one month after the intervention)

Secondary Outcomes (1)

• Client Satisfaction Questionnaire (CSQ-8)

  post-intervention (immediately after the intervention)

Study Arms (2)

Control group

ACTIVE COMPARATOR

The treatment received is a combination of physiotherapy and conventional occupational therapy sessions two days a week, with a duration of 60 minutes divided into 30 minutes of physiotherapy and 30 minutes of occupational therapy.

Procedure: Occupational Therapy and Physiotherapy conventional

Experimental Group

EXPERIMENTAL

The experimental group received 60 minutes of conventional rehabilitation combined with the Pilates Method, divided into 20 minutes of physiotherapy, 20 minutes of occupational therapy and 20 minutes of Pilates Method.

Procedure: Neuropilates+occupational therapy and physiotherapy conventional

Interventions

Neuropilates+occupational therapy and physiotherapy conventional PROCEDURE

Participants assigned to the experimental group received 60 minutes of conventional rehabilitation combined with the Pilates Method, divided into 20 minutes of physical therapy, 20 minutes of occupational therapy and 20 minutes of Pilates Method. Pilates routines will be performed on a mat through the practice of Pilates activation exercises. Each participant will be given the necessary adaptations of each exercise according to their difficulties/disabilities.

Experimental Group

Occupational Therapy and Physiotherapy conventional PROCEDURE

Conventional physical therapy in both groups will include stretching techniques and muscle activation of the lower limb and gait reeducation. Conventional occupational therapy will include stretching techniques and muscle activation in the upper limb as well as training in activities of daily living and functional activities of the upper limb.

Control group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• present a diagnosis of ischemic or hemorrhagic stroke with a minimum evolution of 3 months;
• be over 18 years of age;
• regularly attend rehabilitation treatment at the Physiocare Madrid center;
• present moderate functional problems (score greater than 65 on the Barthel Index);
• not present moderate cognitive impairment (Mini Mental State Examination less than 18 points);
• not present nasogastric tubes;
• accept to participate voluntarily in the study and sign the informed consent form;
• be able to participate in the study and sign the informed consent form.

You may not qualify if:

• time of evolution of less than 3 months;
• other conditions of the central nervous system (tumors, anoxia, cranioencephalic trauma, etc.);
• cardiorespiratory or neurodegenerative disorders, severe brain damage or a score of 6 or higher on the Reisberg Deterioration Scale (GDS);
• a severely impaired level of consciousness or a score of 8 or lower on the Glasgow Coma Scale (GCS);
• receiving other complementary rehabilitative therapy;
• a severe deterioration in the level of consciousness or a score of 8 or lower on the Glasgow Coma Scale (GCS);
• a severe deterioration in the level of consciousness or a score of 8 or lower on the Glasgow Coma Scale (GCS);
• a severe deterioration in the level of consciousness or a score of 8 or lower on the Glasgow Coma Scale (GCS).

Sponsors & Collaborators

• Universidad Rey Juan Carlos: lead

Study Sites (1)

Physiocare Madrid

Madrid, 28047, Spain

Location

MeSH Terms

Conditions

Stroke

Interventions

Occupational Therapy

Condition Hierarchy (Ancestors)

Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases

Intervention Hierarchy (Ancestors)

Rehabilitation; Aftercare; Continuity of Patient Care; Patient Care; Therapeutics

Study Officials

• Sara García-Bravo

  Universidad Rey Juan Carlos

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: PhD Physiotherapist

Study Record Dates

• First Submitted: October 28, 2023
• First Posted: November 13, 2023
• Study Start: July 1, 2023
• Primary Completion: July 24, 2023
• Study Completion: November 15, 2023
• Last Updated: November 13, 2023

Record last verified: 2023-11

Data Sharing

• IPD Sharing: Will not share

Locations

ES (1)