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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05543213
Other study ID # 26181
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date October 1, 2024

Study information

Verified date November 2023
Source Shiraz University of Medical Sciences
Contact Misagh Rahimi, B.Sc.in OT
Phone 9175574547
Email misaghrahimi1995@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Action observation therapy is a new method in rehabilitation that causes motor retraining by activating mirror neurons while watching the activity on the screen and then practicing them. We will use action observation therapy to improve balance and walking in MS patients.


Description:

Multiple sclerosis (MS) is an inflammatory disease of the brain and spinal cord caused by damage to myelin. While the underlying cause of this disease is unknown, a significant relationship has been reported between a series of (CNS) neurons of the central nervous system, immune factors, genetics, and viruses. The primary complaint of MS patients is movement problems, particularly walking disorders, which greatly affect their quality of life, and its improvement is one of the main goals of rehabilitation. Action observation therapy is a new approach. It is used to treat neurological disorders such as cerebral palsy, Parkinson's disease, strokes, and multiple sclerosis. In this method, a video of some purposeful movements and activities recorded by healthy people doing them is shown to the patient, then the person must try to imitate and perform those actions, which causes movement retraining and memory recall. Based on the studies conducted on the effectiveness of neurological treatment methods and proving the effectiveness of this method on other conditions, also considering the involvement of the nervous system in MS and the lack of related studies, we conducted this study with regard to To design a low cost, availability, and ease of use therapeutic method on balance and walking in patients with multiple sclerosis. This study will be conducted on two groups of MS patients. after passing 30 minutes of usual rehabilitation by the blind therapist. One group will watch videos related to action observation exercises and then practice, and for the second group, a video of natural scenery will be shown for the same length of time, then they will practice exercises similar to the first group.


Recruitment information / eligibility

Status Recruiting
Enrollment 28
Est. completion date October 1, 2024
Est. primary completion date July 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Diagnosis of spastic primary progressive, secondary progressive, relapsing-remitting MS - EDSS (Extensive Disability Status Scale) Score between 3 and 6 - MMSE (Mini-mental state examination) test score> 24 Exclusion Criteria: - Recurrence of MS during 3 months before intervention - Pregnancy and lactation - Having a psychiatric disorder or drug/alcohol abuse - Changes in the symptoms of MS during the study period - Inability to sit without torso support - Inability to stand for at least 10 seconds with support - Other neurological or orthopedic diseases of the lower extremities (musculoskeletal diseases, severe osteoarthritis, peripheral neuropathy, joint replacement) - Cardiovascular diseases (recent myocardial infarction, heart failure, uncontrolled hypertension, orthostatic hypotension) - participation in other clinical studies

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Action Observation Therapy
A video clip of a series of exercises is shown to the patients, then they practice them according to mirror neurons and observational learning.

Locations

Country Name City State
Iran, Islamic Republic of School of Rehabilitation Sciences Shiraz Fars

Sponsors (1)

Lead Sponsor Collaborator
Shiraz University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Berg Balance Scale The Berg Balance Scale (BBS) is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function and takes approximately 20 minutes to complete. It does not include the assessment of gait. 30 minutes
Primary Barthel Index The Barthel Scale/Index (BI) is an ordinal scale used to measure performance in activities of daily living (ADL). Ten variables describing ADL and mobility are scored, a higher number being a reflection of greater ability to function independently following hospital discharge.Time taken and physical assistance required to perform each item are used in determining the assigned value of each item. The Barthel Index measures the degree of assistance required by an individual on 10 items of mobility and self care ADL. 25 minutes
Primary Functional Independence Measure (FIM) The Functional Independence Measure (FIM) is an instrument that was developed as a measure of disability for a variety of populations and is not specific to any diagnosis. The FIM instrument
Includes measures of independence for self-care, including sphincter control, transfers, locomotion, communication, and social cognition.
Is an 18-item, seven-level, ordinal scale intended to be sensitive to changes over the course of a comprehensive inpatient medical rehabilitation program.
Uses the level of assistance an individual needs to grade functional status from total independence to total assistance).
The tool is used to assess a patient's level of disability as well as a change in patient status in response to rehabilitation or medical intervention.
20 minutes
Secondary Fatigue Assessment Scale (FAS) The Fatigue Assessment Scale (FAS) is a 10-item self-report scale evaluating symptoms of chronic fatigue. The FAS treats fatigue as a unidimensional construct and does not separate its measurement into different factors. However, in order to ensure that the scale evaluates all aspects of fatigue, it measures both physical and mental symptoms. 10 minutes
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