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

H

Hacettepe University

Status

Completed

Conditions

Multiple Sclerosis

Treatments

Other: Action Observation training
Other: Motor Imagery training
Other: standard rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

It was planned to examine the effects of motor imagery and action observation applied in addition to standard rehabilitation in individuals with Multiple Sclerosis on walking, fatigue, and muscle oxygenation.

Enrollment

48 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

48 participants in 3 patient groups

Motor Imagery Group
Experimental group
Description:
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.
Treatment:
Other: standard rehabilitation
Other: Motor Imagery training
Action Observation Group
Experimental group
Description:
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.
Treatment:
Other: standard rehabilitation
Other: Action Observation training
Control Group
Other group
Description:
Individuals included in this group will receive only 40 minutes of standard rehabilitation. Patients will be trained 3 days a week for 6 weeks.
Treatment:
Other: standard rehabilitation

Trial contacts and locations

1

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Central trial contact

Melike Sumeyye Ozen, M.Sc.

Data sourced from clinicaltrials.gov

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