Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
23 participants
INTERVENTIONAL
2022-11-25
2024-03-05
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Digital symptom mapping and biofeedback treatment
Digital symptom mapping and biofeedback treatment
Digital symptom mapping and biofeedback treatment
Interventions
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Digital symptom mapping and biofeedback treatment
Digital symptom mapping and biofeedback treatment
Eligibility Criteria
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Inclusion Criteria
* Mild TBI as defined by having sustained a head injury with observed or self-reported alteration of consciousness, amnesia, or other relevant acute symptoms.
* PPCS according to the ICD-10 research criteria and PTH according to International Classification of Headache Disorders 3rd edition (ICHD-3). Operationalized as reporting 3 or more symptoms (including headache) on a moderate or greater intensity level on the RPSQ.
* Proficient in Norwegian language (oral and written)
* Signed informed consent
Exclusion Criteria
* Less than three months of experience with smartphones
* Not having access to an iOS or Android smartphone
18 Years
ALL
No
Sponsors
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St. Olavs Hospital
OTHER
Responsible Party
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Locations
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St. Olavs Hospital
Trondheim, , Norway
Countries
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Other Identifiers
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422538
Identifier Type: -
Identifier Source: org_study_id
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