The Effects of Action Observation Therapy (AOT) on Balance and Gait in Patients With Multiple Sclerosis.

Sponsor
Shiraz University of Medical Sciences (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05543213
Collaborator
(none)
28
1
2
5.9
4.7

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Action Observation Therapy
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
28 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effects of Action Observation Therapy (AOT) on Balance and Gait in Patients With Multiple Sclerosis.
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Apr 1, 2023
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group

Videos of nature will be shown to them, and exercises similar to those in the intervention group will be practiced with them.

Active Comparator: Action Observation group

In the intervention group, the same exercises related to balance and walking are practiced after watching videos of the exercises

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.

Outcome Measures

Primary Outcome Measures

  1. Berg Balance Scale [30 min]

    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.

  2. Barthel Index [25 min]

    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.

  3. Functional Independence Measure (FIM) [20 min]

    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.

Secondary Outcome Measures

  1. Fatigue Assessment Scale (FAS) [10 min]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 School of Rehabilitation Sciences Shiraz Fars Iran, Islamic Republic of 7194733669

Sponsors and Collaborators

  • Shiraz University of Medical Sciences

Investigators

  • Study Chair: Mohammad Taghi Karimi, PhD in OP, Full professor of orthotics and prosthetics

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Misagh Rahimi, Occupational Therapy expert, Shiraz University of Medical Sciences
ClinicalTrials.gov Identifier:
NCT05543213
Other Study ID Numbers:
  • 26181
First Posted:
Sep 16, 2022
Last Update Posted:
Sep 16, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Misagh Rahimi, Occupational Therapy expert, Shiraz University of Medical Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2022