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Characterization of Headache and Dizziness Exacerbation Following Mental Imagery in Patients With Persistent Post-Concussive Symptoms

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Current patients of Reut Rehabilitation Hospital or individuals who were discharged from the hospital within the past 12 months.

• Diagnosis of mild Traumatic Brain Injury, concussion, blast injury, or cervical whiplash injury.

• More than 3 months since the event.

• Presence of headaches and/or dizziness that began after the injury and have persisted continuously or intermittently.

• Exclusion of other potential causes of headaches, such as non-healed fractures, chronic inflammation/infection, increased intracranial pressure, or meningeal injury.

• Headache intensity of at least 3/10 on the VAS scale.

Locations
Other Locations
Israel
Reuth Rehabilitation Hospital
RECRUITING
Tel Aviv
Contact Information
Primary
Yotam Yanai, BPT
yanayot@gmail.com
972523993918
Backup
Gali Pinsky, BPT
galipinsky95@gmail.com
972546326566
Time Frame
Start Date: 2025-09-07
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 60
Treatments
Experimental: Mental Imagery Provocation Testing
Provocation Test for Symptoms Using Mental Imagery:~1. Baseline symptom intensity (dizziness/headache) will be measured using the VAS scale.~2. Instruction to perform the movement that is hypothesized to provoke the symptom in reality for approximately 10-20 seconds~3. Measurement of symptom intensity using the VAS scale following the provoked movement.~4. Rest period of several minutes.~5. Measurement of symptom intensity following rest using the VAS scale.~6. Instruction to mentally imagine the movement or scenario hypothesized to provoke the symptom in reality for approximately 10-20 seconds~7. Measurement of symptom intensity using the VAS scale following mental imagery.~8. Measurement of imagery vividness using the VAS-V scale.
Related Therapeutic Areas
Sponsors
Leads: Reuth Rehabilitation Hospital

This content was sourced from clinicaltrials.gov