Virtual Reality for Neglect Diagnostics

NCT ID: NCT01399073

Last Updated: 2018-11-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

27 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-05-31

Study Completion Date

2012-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Compared to the classical "paper and pencil"-tests, testing patients in our virtual reality setup might have a higher sensitivity and specificity.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Spatial Neglect Stroke

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Patients with Neglect

virtual reality setup

Intervention Type BEHAVIORAL

testing for neglect in a virtual reality setup

paper and pencil tests

Intervention Type BEHAVIORAL

testing for neglect with the classical paper-and-pencil tests

c-mri

Intervention Type OTHER

structural and functional (resting state) imaging

Patients with Hemianopsia

virtual reality setup

Intervention Type BEHAVIORAL

testing for neglect in a virtual reality setup

paper and pencil tests

Intervention Type BEHAVIORAL

testing for neglect with the classical paper-and-pencil tests

c-mri

Intervention Type OTHER

structural and functional (resting state) imaging

Healthy age-matched controls

virtual reality setup

Intervention Type BEHAVIORAL

testing for neglect in a virtual reality setup

paper and pencil tests

Intervention Type BEHAVIORAL

testing for neglect with the classical paper-and-pencil tests

c-mri

Intervention Type OTHER

structural and functional (resting state) imaging

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

virtual reality setup

testing for neglect in a virtual reality setup

Intervention Type BEHAVIORAL

paper and pencil tests

testing for neglect with the classical paper-and-pencil tests

Intervention Type BEHAVIORAL

c-mri

structural and functional (resting state) imaging

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* age ≥18 and \<80 years
* first stroke
* neglect symptoms
* no hemianopsia symptoms
* consent given by the patient


* age ≥18 and \<80 years
* first stroke
* no neglect symptoms
* hemianopsia symptoms
* consent given by the patient


* age ≥18 and \<80 years
* no neurological deficits
* informed consent

Exclusion Criteria

* language comprehension deficits
* motor deficits of the upper extremities
* cognitive impairments (MMSE \<20 or SKT \>15 or DEMTEC \>12)
* depression
* seizure disorders
* claustrophobia
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Median Klinik Kladow

UNKNOWN

Sponsor Role collaborator

Freie Universität Berlin

OTHER

Sponsor Role collaborator

Berlin Center for Advanced Neuroimaging

UNKNOWN

Sponsor Role collaborator

Humboldt-Universität zu Berlin

OTHER

Sponsor Role collaborator

NeuroCure Clinical Research Center, Charite, Berlin

OTHER

Sponsor Role collaborator

Charite University, Berlin, Germany

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Andreas Meisel

Prof. Dr. Andreas Meisel

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Andreas Meisel, MD

Role: PRINCIPAL_INVESTIGATOR

Charite University (Center for Stroke Research Berlin CSB & NeuroCure Clinical Research Center NCRC)

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Charité University Medicine

Berlin, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

References

Explore related publications, articles, or registry entries linked to this study.

Ulm L, Wohlrapp D, Meinzer M, Steinicke R, Schatz A, Denzler P, Klehmet J, Dohle C, Niedeggen M, Meisel A, Winter Y. A circle-monitor for computerised assessment of visual neglect in peripersonal space. PLoS One. 2013 Dec 12;8(12):e82892. doi: 10.1371/journal.pone.0082892. eCollection 2013.

Reference Type RESULT
PMID: 24349387 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

KMS-Neglect

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Prospective Memory Imaging
NCT01638884 UNKNOWN NA
AI-powered Portable MRI Abnormality Detection
NCT06803420 NOT_YET_RECRUITING NA
Sport-Related Concussion Recovery in Athletes
NCT06852300 ENROLLING_BY_INVITATION