NCT07656844

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
43

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2025

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2026

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

June 14, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 18, 2026

Completed
Last Updated

June 24, 2026

Status Verified

June 1, 2026

Enrollment Period

11 months

First QC Date

June 14, 2026

Last Update Submit

June 20, 2026

Conditions

Keywords

StrokeDysphagiaPost-stroke dysphagiaOropharyngeal dysphagiaMotor imageryAction observationSwallowing rehabilitationVideofluoroscopic swallowing studyPenetration-Aspiration ScaleGugging Swallowing Screen

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

EXPERIMENTAL

Participants 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.

Behavioral: Video-Assisted Motor ImageryBehavioral: Conventional Dysphagia Rehabilitation

Motor Imagery Alone Group

EXPERIMENTAL

Participants 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.

Behavioral: Motor Imagery TrainingBehavioral: Conventional Dysphagia Rehabilitation

Control Group

ACTIVE COMPARATOR

Participants in this group received conventional dysphagia rehabilitation alone. The rehabilitation program was administered twice weekly for 4 weeks.

Behavioral: Conventional Dysphagia Rehabilitation

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.

Video-Assisted Motor Imagery Group

Participants performed mental imagery of swallowing without visual stimulation. This intervention was added to conventional dysphagia rehabilitation.

Motor Imagery Alone Group

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.

Control GroupMotor Imagery Alone GroupVideo-Assisted Motor Imagery Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

Location

MeSH Terms

Conditions

Deglutition DisordersStroke

Condition Hierarchy (Ancestors)

Esophageal DiseasesGastrointestinal DiseasesDigestive System DiseasesPharyngeal DiseasesOtorhinolaryngologic DiseasesCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Gizem Karcı Aktekin, MD

    Ankara Etlik City Hospital, Physical Medicine and Rehabilitation Clinic

    PRINCIPAL INVESTIGATOR

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
Model Details: Participants were randomly assigned to one of three parallel groups: video-assisted motor imagery plus conventional dysphagia rehabilitation, motor imagery alone plus conventional dysphagia rehabilitation, or conventional dysphagia rehabilitation alone.
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.

Locations