Motor Imagery in Post-Stroke Dysphagia
MI-PSD
The Effect of Motor Imagery on Swallowing Functions in Patients With Post-Stroke Dysphagia: A Single-Blind Randomized Controlled Study
1 other identifier
interventional
43
1 country
1
Brief Summary
This study evaluated the effects of motor imagery added to conventional swallowing rehabilitation in patients with dysphagia after stroke. Dysphagia, or swallowing difficulty, is a common problem after stroke and may increase the risk of aspiration, pneumonia, malnutrition, dehydration, and reduced quality of life. Participants with post-stroke dysphagia were randomly assigned to one of three groups: video-assisted motor imagery, motor imagery alone, or control. All participants received conventional swallowing rehabilitation. In addition, the video-assisted motor imagery group watched videos showing swallowing-related actions and then mentally imagined the observed movement. The motor imagery alone group performed mental imagery of swallowing without visual stimulation. The control group received only conventional swallowing rehabilitation. The intervention period lasted 4 weeks, with sessions performed twice weekly. Swallowing function was assessed before and after treatment using the Gugging Swallowing Screen, the Penetration-Aspiration Scale based on videofluoroscopic swallowing study, and the Stroke Impact Scale. The aim of the study was to determine whether motor imagery, especially when supported by video observation, provides additional benefit for swallowing recovery in patients with post-stroke dysphagia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 31, 2026
CompletedFirst Submitted
Initial submission to the registry
June 14, 2026
CompletedFirst Posted
Study publicly available on registry
June 18, 2026
CompletedJune 24, 2026
June 1, 2026
11 months
June 14, 2026
June 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Penetration-Aspiration Scale Score
Change in swallowing safety was assessed using the Penetration-Aspiration Scale based on videofluoroscopic swallowing study. The scale evaluates airway invasion during swallowing. Scores range from 1 to 8, with higher scores indicating greater penetration or aspiration severity. A decrease in score indicates improvement.
Baseline and Week 4 (end of intervention)
Secondary Outcomes (2)
Change in Gugging Swallowing Screen Score
Baseline and Week 4 (end of intervention)
Change in Stroke Impact Scale Score
Baseline and Week 4 (end of intervention)
Study Arms (3)
Video-Assisted Motor Imagery Group
EXPERIMENTALParticipants in this group received conventional dysphagia rehabilitation plus video-assisted motor imagery. They watched videos depicting swallowing-related actions and then mentally simulated the observed swallowing movement. The intervention was administered twice weekly for 4 weeks.
Motor Imagery Alone Group
EXPERIMENTALParticipants in this group received conventional dysphagia rehabilitation plus motor imagery training without visual stimulation. They were instructed to mentally imagine the swallowing movement. The intervention was administered twice weekly for 4 weeks.
Control Group
ACTIVE COMPARATORParticipants in this group received conventional dysphagia rehabilitation alone. The rehabilitation program was administered twice weekly for 4 weeks.
Interventions
Participants watched videos showing swallowing-related actions and then performed motor imagery by mentally simulating the observed swallowing movement. This intervention was added to conventional dysphagia rehabilitation.
Participants performed mental imagery of swallowing without visual stimulation. This intervention was added to conventional dysphagia rehabilitation.
Conventional dysphagia rehabilitation included standard swallowing therapy approaches used in clinical practice, such as swallowing exercises, compensatory strategies, postural adjustments, and diet or consistency modifications when appropriate.
Eligibility Criteria
You may qualify if:
- Age 18 years or older
- Diagnosis of stroke by a neurologist based on medical history, physical examination, and brain computed tomography and/or magnetic resonance imaging findings
- No progressive or non-progressive neurological disease other than stroke
- No known psychiatric disease
- No sensory dysfunction
- No communication problem
- Mini-Mental State Examination score of 24 or higher and ability to follow commands at a level sufficient to comply with motor imagery practice
- Ability to maintain sitting balance and remain in a sitting position for 30 minutes
- Presence of dysphagia symptoms or need for further evaluation based on dysphagia screening tests, with referral for videofluoroscopic swallowing study
- No serious acute medical condition such as hemodynamic instability during testing
You may not qualify if:
- Refusal to participate in the study or withdrawal from the study during the study period
- Inadequate performance of videofluoroscopic swallowing evaluation due to technical, clinical, or patient compliance-related reasons
- Presence of sensory-motor aphasia
- Presence of visual or hearing impairment
- Presence of severe neglect
- Evidence of esophageal dysphagia on videofluoroscopy and/or clinical symptoms
- History of surgery, cancer, or radiotherapy in the head and neck region that may affect swallowing
- Presence of vertebral problems that may restrict cervical movement, such as advanced cervical discopathy, prominent osteophyte formation, or cervical deformity
- Presence of neurological diseases other than stroke that may cause dysphagia, such as dementia, Parkinson disease, multiple sclerosis, or neuromuscular disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara Etlik City Hospital, Physical Medicine and Rehabilitation Clinic
Ankara, Ankara, 06170, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gizem Karcı Aktekin, MD
Ankara Etlik City Hospital, Physical Medicine and Rehabilitation Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The study was designed as a single-blind trial. Outcome assessments were performed by an assessor who was blinded to group allocation.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Investigator / Principal Investigator
Study Record Dates
First Submitted
June 14, 2026
First Posted
June 18, 2026
Study Start
July 1, 2025
Primary Completion
May 31, 2026
Study Completion
May 31, 2026
Last Updated
June 24, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared.