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Feasibility Study of Deep Brain Recordings for Learning and Memory

A Feasibility Study of Deep Brain Recordings for Learning and Memory

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02417727
Enrollment
0
Registered
2015-04-16
Start date
2015-03-23
Completion date
2018-06-30
Last updated
2019-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Movement Disorders

Keywords

MEMORY TESTING, Biomarkers, Learning

Brief summary

Background: \- Some people with movement disorders are in another NIH protocol. They will have electrodes placed in deep brain areas. They may do tasks before, during, and after surgery. Researchers want to learn more about how brain cells and networks work while people learn and remember. They want to use the data from the other NIH study to do this. Objective: \- To share data from before and during deep brain stimulation surgery. The data will be used in a study of how the brain learns and remembers. Eligibility: \- People at least 18 years old who are in protocol 11-N-0211 and have certain movement disorders. Design: * As part of protocol 11-N-0211, data on participants brainwave activity is collected. In this protocol, they will have that data stored and shared. * Researchers will access imaging data from deep brain stimulation surgery. * Researchers will access other medical records.

Detailed description

OBJECTIVES: The purpose of this protocol is to share neural data collected before and during deep brain stimulation surgery with the University of Pennsylvania to identify biomarkers of successful learning and memory. STUDY POPULATION: Up to twenty (20) adult subjects who are participating in NIH protocol 11-N-0211 Deep Brain Stimulation Surgery for Movement Disorders who provide written informed consent for sharing and the additional use of their data. STUDY DESIGN: This protocol only involves providing consent to share learning and memory data collected under Protocol 11-N-0211. There are no separate or additional participant procedures involved in this protocol.

Interventions

None listed

Sponsors

National Institute of Neurological Disorders and Stroke (NINDS)
Lead SponsorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* INCLUSION CRITERIA: Adults at least age 18 Currently enrolled in 11-N-0211

Exclusion criteria

Unable to provide own informed consent

Design outcomes

Primary

MeasureTime frame
Permission to share data from partiicpation on NIH protocol #11-N-0211ongoing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026