NCT01113944

Brief Summary

We are testing whether various cognitive training procedures can enhance cognition and brain function

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
75

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2010

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2010

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

April 28, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

April 30, 2010

Completed
4.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2014

Completed
Last Updated

November 26, 2014

Status Verified

November 1, 2014

Enrollment Period

4.6 years

First QC Date

April 28, 2010

Last Update Submit

November 25, 2014

Conditions

Outcome Measures

Primary Outcomes (1)

  • MRI

    Functional and structural MR images will be acquired

    2 hours Pre and Post intervention

Study Arms (2)

Program 1

ACTIVE COMPARATOR

Program 1

Behavioral: Program 1

Program 2

ACTIVE COMPARATOR

Program 2

Behavioral: Program 2

Interventions

Program 1BEHAVIORAL
Program 1
Program 2BEHAVIORAL
Program 2

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • Neurological conditions
  • pregnancy
  • metalic implants

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Massachusettts General Hospital

Boston, Massachusetts, 02129, United States

Location

Study Officials

  • Sara Lazar, PhD

    MGH

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Research Scientist

Study Record Dates

First Submitted

April 28, 2010

First Posted

April 30, 2010

Study Start

April 1, 2010

Primary Completion

November 1, 2014

Study Completion

November 1, 2014

Last Updated

November 26, 2014

Record last verified: 2014-11

Locations