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Clinical Trials/NCT05377476
NCT05377476CompletedNot Applicable

Investigation of the Effects of Motor Imagery and Action Observation in People With Multiple Sclerosis

Hacettepe University1 site in 1 country48 target enrollmentStarted: June 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
48
Locations
1
Primary Endpoint
6 Min Walking Test

Study Overview

Brief Summary

It was planned to examine the effects of motor imagery and action observation applied in addition to standard rehabilitation in people with multiple sclerosis on walking, fatigue, and trunk control.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Being between the ages of 18-65
  • A definitive diagnosis of MS by a neurologist according to the 2017 McDonald Criteria
  • Expanded Disability Status Scale (EDSS) score of 4.0 and below (it is determined routinely by the physician during the examination)
  • Not having an attack in the last 3 months
  • A minimum score of 4 in each motor imagery ability (internal visual imagery, external visual imagery, and kinesthetic imagery) on the Movement Imagery Questionnaire-3 (MIQ-3)

Exclusion Criteria

  • cognitive impairment, defined as a Mini-Mental State Examination (MMSE) score of less than 24
  • Having another musculoskeletal, cardiovascular, pulmonary, metabolic, or neurological disease severe enough to preclude participation in the study.
  • Having severe vision and hearing problems

Arms & Interventions

Motor Imagery Group

Experimental

Individuals included in this group will receive 20 minutes of motor imagery training in addition to 40 minutes of standard rehabilitation. Patients will be trained 3 days a week for 6 weeks.

Intervention: Motor Imagery training (Other)

Motor Imagery Group

Experimental

Individuals included in this group will receive 20 minutes of motor imagery training in addition to 40 minutes of standard rehabilitation. Patients will be trained 3 days a week for 6 weeks.

Intervention: standard rehabilitation (Other)

Action Observation Group

Experimental

Individuals included in this group will receive 20 minutes of action observation training in addition to 40 minutes of standard rehabilitation. Patients will be trained 3 days a week for 6 weeks.

Intervention: Action Observation training (Other)

Action Observation Group

Experimental

Individuals included in this group will receive 20 minutes of action observation training in addition to 40 minutes of standard rehabilitation. Patients will be trained 3 days a week for 6 weeks.

Intervention: standard rehabilitation (Other)

Control Group

Other

Individuals included in this group will receive only 40 minutes of standard rehabilitation. Patients will be trained 3 days a week for 6 weeks.

Intervention: standard rehabilitation (Other)

Outcomes

Primary Outcomes

6 Min Walking Test

Time Frame: 6 week

It will be used to measure walking distance. Before the test is administered, individuals will be given the necessary information and will be asked to walk as fast as possible on a 30-meter track for 6 minutes.

Secondary Outcomes

  • Fatigue Severity Scale(6 week)
  • Trunk Impairment Scale(6 week)
  • Timed Up and Go Test(6 week)
  • Multiple Sclerosis Walking Scale-12(6 week)
  • Timed Up and Go Test(6 week)
  • Multiple Sclerosis Walking Scale-12(6 week)
  • RehaGait® (Hasomed, Magdeburg, Germany) Gait Analysis(6 week)
  • Fatigue Severity Scale(6 week)
  • Trunk Impairment Scale(6 week)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Melike Sumeyye Ozen

Research Assistant

Bandırma Onyedi Eylül University

Study Sites (1)

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