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Completed

NCT Number: NCT02081508

Consolidation & Interference in Multiple Sclerosis

The purpose of this research study is to investigate whether minimizing interference improves memory in multiple sclerosis.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kessler Foundation

West Orange, New Jersey, 07052, United States

About this study

The ability to form new long-lasting memories is important for successful independent living and a high quality of life. Roughly half of the individuals diagnosed with Multiple Sclerosis (MS) have difficulty remembering new information and this is likely associated with poor acquisition of new information. There are only a limited number of studies that have investigated memory consolidation in MS. The current study will investigate the role of interference during the consolidation time period of memory formation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • If you are between the ages of 18-65.
  • 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 younger than 18 years old.
  • 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.

Treatment and study plan

Interference onset

Behavioral

Temporal duration of interference onset.

Primary outcomes

  1. Recall Proportion

    Time frame: 2 hours

Sponsors and collaborators

Lead sponsor

Kessler Foundation

Other

Registry information

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Mar 7, 2014
Registry last updated
Aug 1, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.