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Efficacy Study of Cognitive Intervention in Amnestic Mild Cognitive Impairment

NCT01358955 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 293

Last updated 2013-08-28

No results posted yet for this study

Summary

* There will be a significant difference in cognitive function between cognitive intervention group (group therapy) and a wait list control group.
* There will be a significant difference in cognitive function between a home-based cognitive intervention group and a wait list control group.

Conditions

Interventions

OTHER

group cognitive intervention

The cognitive training will be administered twice a week for 12 weeks, located in hospital-based outpatient memory clinics. Each session will last approximately 90 minutes. The cognitive training programs will be offered in group sessions consisted of 5 participants.

OTHER

Home-based cognitive intervention

The participants will do their paper and pencil homework for 30 minutes every business days for 12 weeks.

Sponsors & Collaborators

  • Eisai Inc.

    collaborator INDUSTRY

  • Inha University Hospital

    lead OTHER

Principal Investigators

  • Seong H Choi, MD, PhD · Inha University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01358955 on ClinicalTrials.gov