We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Training in the Workplace

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01113944
First Posted: April 30, 2010
Last Update Posted: November 26, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Sara W Lazar, Massachusetts General Hospital
  Purpose
We are testing whether various cognitive training procedures can enhance cognition and brain function

Condition Intervention
Healthy Individuals Behavioral: Program 1 Behavioral: Program 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Outcomes Assessor)
Primary Purpose: Basic Science
Official Title: Training in the Workplace

Further study details as provided by Sara W Lazar, Massachusetts General Hospital:

Primary Outcome Measures:
  • MRI [ Time Frame: 2 hours Pre and Post intervention ]
    Functional and structural MR images will be acquired


Enrollment: 75
Study Start Date: April 2010
Study Completion Date: November 2014
Primary Completion Date: November 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Program 1
Program 1
Behavioral: Program 1
Active Comparator: Program 2
Program 2
Behavioral: Program 2

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy individuals aged 18-50 years old
  • Right handed
  • Must have reliable internet access from a desktop computer with webcam
  • English speaking

Exclusion Criteria:

  • Neurological conditions
  • pregnancy
  • metalic implants
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01113944


Locations
United States, Massachusetts
Massachusettts General Hospital
Boston, Massachusetts, United States, 02129
Sponsors and Collaborators
Massachusetts General Hospital
Investigators
Principal Investigator: Sara Lazar, PhD MGH
  More Information

Responsible Party: Sara W Lazar, Associate Research Scientist, Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT01113944     History of Changes
Other Study ID Numbers: YEL1
First Submitted: April 28, 2010
First Posted: April 30, 2010
Last Update Posted: November 26, 2014
Last Verified: November 2014