- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07331896
Strategy Training for Optimizing Attention for Individuals With Spatial Neglect (SOAR)
May 8, 2026 updated by: Emily Grattan, University of Pittsburgh
Examining Strategy Training for Optimizing Attention in Rehabilitation for Community-Dwelling Individuals With Spatial Neglect
It is common for individuals after stroke to have a cognitive perceptual impairment called unilateral spatial neglect (neglect).
Individuals with neglect have difficulty paying attention to one side of their body or one side of the environment and therefore experience difficulty performing daily activities.
There are a lack of effective treatments for neglect and new interventions are needed to help reduce disability for these individuals.
Metacognitive strategy training (strategy training) is an intervention that has the potential to reduce neglect-related disability and improve individuals' attention and awareness of their neglect.
This study seeks to examine the effects of strategy training on neglect, self-awareness, and disability, specifically for individuals who are living in the community after their stroke.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Unilateral spatial neglect (neglect) post stroke is characterized by a lack of attention to one side of the body or one side of the environment.
Individuals with neglect experience significant disability and are often unaware of their neglect symptoms which can make it even more difficult to treat.
There are a lack of effective treatments for neglect and new interventions are needed to help reduce disability for these individuals.
Metacognitive strategy training (strategy training) is an intervention that has the potential to reduce neglect-related disability and improve individuals' attention and awareness of their neglect.
Strategy training teaches individuals to develop personalized goals, self-assess their performance of daily activities, and develop and evaluate strategies designed to overcome barriers and improve their performance of daily activities.
While strategy training shows promise for individuals with neglect, no studies have tailored the intervention for this group of individuals or examined the effects of strategy training for individuals with neglect specifically with individuals living in the community.
This study examines whether strategy training facilitates reductions in neglect and disability and improves self-awareness.
Study Type
Interventional
Enrollment (Estimated)
45
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 Contact
- Name: Emily Grattan, PhD, OTRlL
- Phone Number: 412-648-0619
- Email: esg39@pitt.edu
Study Locations
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15260
- Recruiting
- University of Pittsburgh
-
-
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:
- had a stroke
- presence of neglect as determined by score of <18 or 2 or more collisions on the Virtual Reality Lateralized Attention Test (VRLAT); score below established cutoff for neglect on one of the six subtests of the Behavioral Inattention Test (BIT); OR reported signs/symptoms of neglect
- ≥18 years old
- lives within 30 miles of the University of Pittsburgh in a community dwelling.
Exclusion Criteria:
- Boston Diagnostic Aphasia Examination (BDAE) Severity Scale score of 0
- dementia per medical record
- active major depressive disorder per medical record
- not willing to be videotaped
- subject is currently receiving rehabilitation therapy as part of their usual care
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: Strategy Training
The strategy training intervention teaches individuals to develop personalized goals, self-assess their performance of daily activities, and develop and evaluate strategies designed to overcome barriers and improve their performance of daily activities.
Participants use a workbook to support their application of the strategy training.
|
This intervention will use an adapted form of strategy training for people with neglect.
|
|
Active Comparator: Attention Control
The attention control intervention controls for the non-specific effects of strategy training.
The study team will administer the standardized and dose-matched protocol, using scripted open-ended questions to facilitate participants' reflections on their rehabilitation activities and experiences.
Participants complete a daily journal, merely reviewing their rehabilitation activities.
|
This intervention will use a reflective listening protocol.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in attention/neglect
Time Frame: Baseline to Post-intervention (up to 60 days)
|
Change in attention/neglect measured with the Catherine Bergego Scale.
Total scores on the Catherine Bergego Scale therapist-rated assessment range from 0-30 (higher=greater neglect).
The a priori criterion for change was a medium effect size of change (Cohen's d≥0.5)
|
Baseline to Post-intervention (up to 60 days)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Client Satisfaction with Strategy Training
Time Frame: Post-intervention (up to 60 days)
|
Client satisfaction is measured using the Client Satisfaction Questionnaire-8.
The a priori criterion for satisfaction was: ≥90% of participants report mean satisfaction score ≥3 on the Client Satisfaction Questionnaire-8 items.
Item scores on the Client Satisfaction Questionnaire-8 range from 0-4.
Higher scores on the Client Satisfaction Questionnaire-8=greater satisfaction.
|
Post-intervention (up to 60 days)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Emily Grattan, PhD, OTR/L, University of Pittsburgh
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)
April 6, 2026
Primary Completion (Estimated)
January 1, 2029
Study Completion (Estimated)
January 1, 2029
Study Registration Dates
First Submitted
December 26, 2025
First Submitted That Met QC Criteria
December 26, 2025
First Posted (Actual)
January 12, 2026
Study Record Updates
Last Update Posted (Actual)
May 12, 2026
Last Update Submitted That Met QC Criteria
May 8, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY25090119
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
At present, there is no plan to share data.
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.
Clinical Trials on Stroke
-
National Assembly ClinicBayero University Kano, NigeriaRecruitingStroke | Stroke Hemorrhagic | Stroke Ischemic | Hemiparesis After StrokeNigeria
-
University of PittsburghRecruitingHemorrhagic Stroke | Embolic Stroke of Undetermined Source | Ischemic Stroke, Cryptogenic | Recurrent Ischemic Stroke | Ischemic Stroke, EmbolicUnited States
-
Mahidol UniversityNot yet recruitingIschemic Stroke | Hemorrhagic Stroke | Subacute Stroke | Chronic Stroke SurvivorsThailand
-
Mahidol UniversityRecruitingIschemic Stroke | Hemorrhagic Stroke | Subacute Stroke | Chronic Stroke PatientThailand
-
University Hospital, GhentRecruitingStroke | Stroke, Ischemic | Stroke, Acute | Stroke Sequelae | Stroke HemorrhagicBelgium
-
Moleac Pte Ltd.Not yet recruitingStroke | Stroke, Ischemic | Stroke Sequelae | Stroke, Cardiovascular | Strokes Thrombotic | Stroke, Embolic | Stroke, Cryptogenic
-
Fondazione Don Carlo Gnocchi OnlusScuola Superiore Sant'Anna di Pisa; Fondazione Policlinico Universitario Campus...Not yet recruitingStroke | Stroke Hemorrhagic | Upper Limb Rehabilitation | Stroke IschemicItaly
-
Samsung Medical CenterCompletedChronic Stroke | Subacute Stroke | ExoskeletonSouth Korea
-
University of Illinois at ChicagoRecruitingStroke, Ischemic | Stroke Hemorrhagic | Stroke, CerebrovascularUnited States
-
IRCCS San Camillo, Venezia, ItalyRecruitingStroke | Stroke, Ischemic | Stroke Sequelae | Stroke HemorrhagicItaly
Clinical Trials on Strategy Training
-
Ibn Haldun UniversityCompletedAnxiety | Depressive Symptoms | Anxiety Disorders and Symptoms | Emotional Dysregulation | SadnessTurkey (Türkiye)
-
MGH Institute of Health ProfessionsLSVT GlobalCompleted
-
University of PittsburghEunice Kennedy Shriver National Institute of Child Health and Human Development...Terminated
-
University of PittsburghCompletedStroke | Adherence, Patient | Strategy TrainingUnited States
-
University of HaifaNot yet recruiting
-
Taipei Medical UniversityActive, not recruitingStroke | Cognitive ImpairmentTaiwan
-
Taipei Medical UniversityActive, not recruitingStroke | Cognitive Impairment | Acquired Brain InjuryTaiwan
-
Centre Hospitalier Universitaire de Saint EtienneRecruitingAcute Coronary SyndromeFrance
-
Rutgers, The State University of New JerseyNational Institute on Aging (NIA)RecruitingAlzheimer's Disease (AD) | Healthy AgingUnited States
-
Taipei Medical UniversityRecruiting