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
53 participants
INTERVENTIONAL
2023-10-01
2024-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Intervention group
Four-week, at-home VR intervention with a recommended daily use of 10-30 minutes
VR (Reducept)
Reducept is a novel VR intervention that consists of a combination of pain neuroscience education (PNE) and pain management techniques. It includes different psychological therapy modalities (e.g. acceptance and commitment therapy (ACT), cognitive behavioral therapy (CBT) and hypnotherapy) into a single application.
Control group
No intervention, patient is a waiting-list control
No interventions assigned to this group
Interventions
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VR (Reducept)
Reducept is a novel VR intervention that consists of a combination of pain neuroscience education (PNE) and pain management techniques. It includes different psychological therapy modalities (e.g. acceptance and commitment therapy (ACT), cognitive behavioral therapy (CBT) and hypnotherapy) into a single application.
Eligibility Criteria
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Inclusion Criteria
* suffering from primary or secondary CMP
* finished with biomedical diagnostics and treatment
* open to biopsychosocial treatment
* willing and capable of complying with study procedures.
Exclusion Criteria
* unable to finish Dutch questionnaires.
18 Years
ALL
No
Sponsors
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University of Twente
OTHER
Responsible Party
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Monique Tabak
Professor
Locations
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Deventer Ziekenhuis
Deventer, Overijssel, Netherlands
Roessingh rehabilitation center
Enschede, Overijssel, Netherlands
Nocepta
Hengelo, Overijssel, Netherlands
Revalidatie Friesland
Emmeloord, Provincie Friesland, Netherlands
Countries
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Other Identifiers
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230405
Identifier Type: -
Identifier Source: org_study_id
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