- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07507383
Dynamic Auditory Cueing for Spatial Neglect in Stroke (DAC-SN)
April 1, 2026 updated by: Elif Ezgi Kurtul, MD, Gazi University
The Effect of Dynamic Auditory Cueing on Spatial Neglect in Patients With Stroke: A Randomized Controlled Trial
Spatial neglect is a common condition after stroke and can make it difficult for people to pay attention to one side of space.
This problem can negatively affect daily activities and functional independence.
This study aims to evaluate whether dynamic auditory cueing for spatial neglect (DAC-SN) can improve spatial neglect in people with stroke.
Participants are randomly assigned to one of two groups.
One group receives conventional rehabilitation, while the other group receives conventional rehabilitation combined with dynamic auditory cueing.
Dynamic auditory cueing uses moving sounds to guide attention toward the affected side.
The intervention is applied for about ten minutes per day, five days a week, for four weeks.
Spatial neglect and functional outcomes are assessed using standardized clinical tests and scales at baseline and at predefined time points during and after the intervention.
The results of this study may provide evidence for the use of auditory-based approaches in the rehabilitation of spatial neglect after stroke.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Detailed Description
Spatial neglect is a common and disabling condition following stroke, characterized by reduced awareness of stimuli on one side of space.
It is associated with impaired functional recovery and decreased independence in daily activities.
Despite conventional rehabilitation approaches, spatial neglect may persist and continues to be a significant challenge in stroke rehabilitation.
Dynamic auditory cueing for spatial neglect (DAC-SN) has been proposed as a method to facilitate attentional orientation by providing external sensory input directed toward the affected side.
This approach may enhance spatial exploration and support recovery by promoting engagement with the neglected hemispace.
The aim of this randomized controlled trial is to investigate the effect of dynamic auditory cueing in patients with stroke and spatial neglect.
Participants are randomly assigned to receive either conventional rehabilitation alone or conventional rehabilitation combined with dynamic auditory cueing.
The intervention is delivered in addition to standard rehabilitation in structured sessions over a four-week period.
The control group receives conventional rehabilitation according to standard clinical practice.
Spatial neglect severity and functional outcomes are assessed using standardized clinical measures at baseline and at predefined time points during and after the intervention period.
The findings of this study are expected to provide evidence on the potential role of auditory-based interventions as an adjunct to conventional rehabilitation in improving spatial neglect and functional outcomes in patients with stroke.
Study Type
Interventional
Enrollment (Actual)
18
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ankara
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Ankara, Ankara, Turkey (Türkiye), 06560
- Gazi University Faculty of Medicine, Department of Physical Medicine and Rehabilitation
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Adults aged 18 years or older
- Subacute or chronic stroke
- Clinical diagnosis of left-sided spatial neglect confirmed by standardized tests (e.g., Line Bisection Test (LBT), Star Cancellation Test (SCT))
- Normal or corrected visual acuity
- Absence of auditory extinction
- Ability to understand and comply with study procedures
- Provision of written informed consent
Exclusion Criteria:
- Hearing impairment (Hearing Handicap Inventory score ≥26)
- Presence of hemianopia
- Impaired visual acuity due to ocular pathology (e.g., cataract, glaucoma)
- History of neurological disease (e.g., dementia, Parkinson's disease)
- Structural brain lesions unrelated to stroke
- Inability to participate in rehabilitation sessions or assessments
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Dynamic Auditory Cueing Group
Participants in this group receive dynamic auditory cueing for spatial neglect (DAC-SN) in addition to their standard conventional rehabilitation program.
The intervention involves exposure to moving environmental sounds (such as animal or transportation noises) designed to redirect attention toward the neglected hemispace.
The intervention is administered for 10 minutes per day, 5 days per week, over a total period of 4 weeks.
|
The intervention consists of structured 10-minute sessions using digitized environmental sounds (e.g., animal sounds, moving vehicles, or sirens) as auditory cues.
Dynamic auditory cueing for spatial neglect (DAC-SN) is applied using sounds presented with a dynamic spatial movement pattern across the horizontal plane.
The auditory stimulus is designed to move from the intact hemispace toward the neglected hemispace or to follow a continuous scanning trajectory to guide attention toward the affected side.
Stimuli are delivered through a stereo headset to ensure clear perception of directional movement.
The intervention is administered in standardized sessions over a four-week period (5 sessions per week).
This approach aims to promote active spatial attention and scanning behavior and differs from conventional static auditory stimulation.
Participants receive standard stroke rehabilitation, including physical and occupational therapy focused on motor function, mobility, and activities of daily living.
This group follows the same rehabilitation schedule as the experimental group but does not receive dynamic auditory cueing for spatial neglect (DAC-SN).
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Active Comparator: Conventional Rehabilitation Group
Participants in this group receive only the standard conventional rehabilitation program provided by the clinic.
This group does not receive dynamic auditory cueing for spatial neglect (DAC-SN).
The frequency and duration of the standard therapy are matched to those of the experimental group to ensure a fair comparison of the additional effects of auditory cueing.
|
Participants receive standard stroke rehabilitation, including physical and occupational therapy focused on motor function, mobility, and activities of daily living.
This group follows the same rehabilitation schedule as the experimental group but does not receive dynamic auditory cueing for spatial neglect (DAC-SN).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Line Bisection Test (LBT) deviation score
Time Frame: Baseline, after 1 session, after 10 sessions, and after 20 sessions (end of treatment)
|
The Line Bisection Test (LBT) is used to assess spatial bias by measuring deviation from the true midpoint of horizontal lines.
Deviation toward the right side indicates more severe left-sided spatial neglect.
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Baseline, after 1 session, after 10 sessions, and after 20 sessions (end of treatment)
|
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Catherine Bergego Scale (CBS) score
Time Frame: Baseline and after 20 sessions (end of treatment)
|
The Catherine Bergego Scale (CBS) is used to assess the impact of spatial neglect on daily activities.
Higher scores indicate greater severity of neglect in functional tasks.
|
Baseline and after 20 sessions (end of treatment)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Star Cancellation Test (SCT) score
Time Frame: Baseline, after 1 session, after 10 sessions, and after 20 sessions (end of treatment)
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The Star Cancellation Test (SCT) is used to assess spatial neglect by measuring the number and spatial distribution of correctly identified targets.
Omission of targets on the left side indicates more severe left-sided spatial neglect.
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Baseline, after 1 session, after 10 sessions, and after 20 sessions (end of treatment)
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Line Cancellation Test (LCT) score
Time Frame: Baseline, after 1 session, after 10 sessions, and after 20 sessions (end of treatment)
|
The Line Cancellation Test (LCT) evaluates spatial neglect by assessing the ability to detect and cancel target lines.
Omission of lines on the left side indicates more severe left-sided spatial neglect.
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Baseline, after 1 session, after 10 sessions, and after 20 sessions (end of treatment)
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Functional Independence Measure (FIM) score
Time Frame: Baseline and after 20 sessions
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The Functional Independence Measure (FIM) assesses functional independence in activities of daily living.
Higher scores indicate greater functional independence.
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Baseline and after 20 sessions
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Center of Cancellation (CoC) value
Time Frame: Baseline, after 1 session, after 10 sessions, and after 20 sessions
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The Center of Cancellation (CoC) quantifies spatial bias based on cancellation task performance.
Higher absolute values indicate more severe spatial neglect.
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Baseline, after 1 session, after 10 sessions, and after 20 sessions
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gulcin Kaymak Karatas, MD, Gazi University Faculty of Medicine, Department of Physical Medicine and Rehabilitation
- Study Director: Elif E Kurtul, MD, Gazi University Faculty of Medicine, Department of Physical Medicine and Rehabilitation
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Van Vleet TM, DeGutis JM. Cross-training in hemispatial neglect: auditory sustained attention training ameliorates visual attention deficits. Cortex. 2013 Mar;49(3):679-90. doi: 10.1016/j.cortex.2012.03.020. Epub 2012 Apr 9.
- Kaufmann BC, Cazzoli D, Bartolomeo P, Frey J, Pflugshaupt T, Knobel SEJ, Nef T, Muri RM, Nyffeler T. Auditory spatial cueing reduces neglect after right-hemispheric stroke: A proof of concept study. Cortex. 2022 Mar;148:152-167. doi: 10.1016/j.cortex.2021.12.009. Epub 2022 Jan 19.
- Golay L, Hauert CA, Greber C, Schnider A, Ptak R. Dynamic modulation of visual detection by auditory cues in spatial neglect. Neuropsychologia. 2005;43(9):1258-65. doi: 10.1016/j.neuropsychologia.2004.12.006. Epub 2005 Feb 5.
- Barrett AM, Burkholder S. Monocular patching in subjects with right-hemisphere stroke affects perceptual-attentional bias. J Rehabil Res Dev. 2006 May-Jun;43(3):337-46. doi: 10.1682/jrrd.2005.01.0015.
- Long J, Zhang Y, Liu X, Gao Q, Pan M. Music-based interventions for unilateral spatial neglect: A systematic review. Neuropsychol Rehabil. 2023 Oct;33(9):1462-1487. doi: 10.1080/09602011.2022.2111314. Epub 2022 Aug 18.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 21, 2024
Primary Completion (Estimated)
April 10, 2026
Study Completion (Estimated)
April 10, 2026
Study Registration Dates
First Submitted
March 27, 2026
First Submitted That Met QC Criteria
March 27, 2026
First Posted (Actual)
April 2, 2026
Study Record Updates
Last Update Posted (Actual)
April 7, 2026
Last Update Submitted That Met QC Criteria
April 1, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GAZI-DAC-2026-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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