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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
39 participants
INTERVENTIONAL
2014-03-31
2015-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Intellectual Enrichment to Build Cognitive Reserve in MS
NCT01978574
Treating New Learning and Memory Deficits in Progressive Multiple Sclerosis (MS)
NCT02301247
Testing the Efficacy of Self-Generation Treatment Protocol
NCT02032589
Cortical Inhibition in Patients With Multiple Sclerosis
NCT07128160
Improving New Learning and Memory in Multiple Sclerosis
NCT00166283
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Unfilled interference
Interference onset: delayed test at 540000 ms
Interference onset
Temporal duration of interference onset.
Early interference
Interference onset: delayed test at 0 ms
Interference onset
Temporal duration of interference onset.
Mid interference
Interference onset: delayed test at 360000 ms
Interference onset
Temporal duration of interference onset.
Late interference
Interference onset: delayed test at 180000 ms
Interference onset
Temporal duration of interference onset.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Interference onset
Temporal duration of interference onset.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* If you have a diagnosis of Multiple Sclerosis (MS) or are medically healthy.
* If you have MS, you have not had a flare up of MS symptoms in the past month.
* You do not have other neurological issues such as, Epilepsy or Stroke.
* You do not have a significant history of psychiatric problems or a current diagnosis of Major Depressive Disorder, Schizophrenia, Bipolar Disorder .
* You do not have a significant history of drug or alcohol abuse.
* You can read and speak English fluently.
* You are not currently taking steroids.
Exclusion Criteria
* You are older than 65 years old.
* You have had a prior stroke or neurological disease other than MS.
* You have a history of significant psychiatric illness (for example, bipolar disorder, schizophrenia, or psychosis) or a current diagnosis of Major Depressive Disorder, Bipolar Disorder.
* You have a significant alcohol or drug abuse history.
* You are currently taking steroids.
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kessler Foundation
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Joshua Sandry
Visiting Scientist Neuropsychology & Neuroscience Research
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kessler Foundation
West Orange, New Jersey, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
R-800-13
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.