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Efficacy of Ubiquitous SR-based Memory Advancement and Rehabilitation Training (U-SMART)

NCT01688128 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2016-04-20

No results posted yet for this study

Summary

The purpose of this study is to examine the efficacy of the Ubiquitous Spaced Retrieval-based Memory Advancement and Rehabilitation Training (U-SMART) in the elderly individuals with mild cognitive impairment (MCI) by an open-label, controlled, crossover Trial.

Conditions

Interventions

DEVICE

Phase I U-SMART (4 wks)

Intervention\_Control Group, 4-weeks U-SMART(2 session/week); Control\_Intervention Group, no intervention

OTHER

Washout (2 wks)

2-weeks wash out period in both arms

DEVICE

Phase II U-SMART (4 wks)

Intervention\_Control Group, no intervention; Control\_Intervention Group, 4-weeks U-SMART(2 session/week, Crossover design)

Sponsors & Collaborators

  • KT Corporation

    collaborator INDUSTRY

  • Seoul National University Bundang Hospital

    lead OTHER

Principal Investigators

  • Ki Woong Kim, M.D., Ph.D. · Seoul National University Bundang Hospital, Seong-nam, Korea

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
55 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2015-12-31
Completion
2015-12-31

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 NCT01688128 on ClinicalTrials.gov