Actively Recruiting
Symptom Exacerbation Following Mental Imagery in Patients With Persistent Post-Concussive Symptoms
Led by Reuth Rehabilitation Hospital · Updated on 2026-04-14
60
Participants Needed
1
Research Sites
68 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Background: Mild Traumatic Brain Injury (mTBI) often results in persistent emotional, cognitive, and somatic symptoms-such as headaches and dizziness. These symptoms impose a significant burden, yet their underlying mechanisms remain unclear. Predictive processing theories suggest that persistent symptoms may result from learned perceptual errors, particularly in individuals with high negative affectivity. This framework may help explain ongoing persistent post-concussive symptoms (PPCS) in the absence of identifiable pathology, which have been linked to various psychological factors. Mental imagery (MI) is thought to engage similar predictive processes. There is evidence that MI of symptom-triggering movements may exacerbate symptoms in individuals with chronic somatic conditions. However, this phenomenon has not been studied in PPCS patients. Investigating symptom provocation through MI may yield novel insights into the neuropsychological mechanisms sustaining PPCS and potentially contribute to the development of therapeutic tools for this population. Objectives: 1. Documenting the exacerbation of headache and dizziness following provocative mental imagery (imagery of movements or scenarios that elicit these symptoms in real life) in patients with PPCS. 2. Comparing changes in headache and dizziness after provocative MI versus neutral MI (imagery of movements or scenarios that do not elicit these symptoms in real life). 3. Comparing patients who experience symptom exacerbation following mental imagery to those who do not. 4. Describing associations between symptom exacerbation and negative affectivity, anxiety, depression, catastrophizing, and lower daily functioning. Methods: A cross-sectional study will be conducted on adult patients experiencing PPCS following mTBI. Participants will be recruited through convenience sampling from a computerized hospital database of Reuth Rehabilitation Hospital, based on inclusion and exclusion criteria. After signing an informed consent form, participants will be invited to attend 2 to 3 sessions, each lasting 1 to 2 hours. During these sessions, a licensed physiotherapist will conduct a comprehensive clinical assessment, including: Completion of self-report questionnaires; A vestibular examination; Anamnestic interview and clinical assessment of individual movement- and scenario-related triggers for dizziness and headaches; Symptom provocation testing using mental imagery of the identified triggers.
CONDITIONS
Official Title
Symptom Exacerbation Following Mental Imagery in Patients With Persistent Post-Concussive Symptoms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Current patients of Reut Rehabilitation Hospital or individuals discharged within the past 12 months
- Diagnosis of mild traumatic brain injury, concussion, blast injury, or cervical whiplash injury
- More than 3 months have passed since the injury event
- Presence of headaches and/or dizziness that started after the injury and persist continuously or intermittently
- Other causes of headaches like fractures, chronic inflammation, increased intracranial pressure, or meningeal injury have been ruled out
- Headache intensity of at least 3 out of 10 on the Visual Analog Scale (VAS)
You will not qualify if you...
- Cognitive impairment preventing informed consent (Mini-Mental State Examination or Montreal Cognitive Assessment score below 20)
- Diagnosed central neurological diseases such as multiple sclerosis, Parkinson's disease, stroke, or brain tumor
- Presence of known pyramidal or extrapyramidal neurological signs
- Significant language difficulties that affect communication
- Psychiatric disorders that significantly impair communication
- Use of vestibular-suppressant medication without willingness or ability to stop it 24 hours before testing
- Oculomotor dysfunction affecting multiple eye movement functions
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Reuth Rehabilitation Hospital
Tel Aviv, Israel
Actively Recruiting
Research Team
Y
Yotam Yanai, BPT
CONTACT
G
Gali Pinsky, BPT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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