Cognitive Screening and Cognitive Training in Seniors
|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.|
|ClinicalTrials.gov Identifier: NCT02588209|
Recruitment Status : Completed
First Posted : October 27, 2015
Last Update Posted : December 7, 2017
|Condition or disease||Intervention/treatment||Phase|
|Mild Cognitive Impairment||Behavioral: Strategic Memory Advanced Reasoning Training Behavioral: Brain Health Workshop||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||71 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Cognitive Screening and Cognitive Training in Seniors|
|Study Start Date :||January 2012|
|Actual Primary Completion Date :||June 2015|
|Actual Study Completion Date :||December 2017|
Experimental: SMART Training
This group will receive the Strategic Memory Advanced Reasoning Training (SMART) program, twice a week for four weeks.
Behavioral: Strategic Memory Advanced Reasoning Training
SMART teaches strategies to improve the ability to process information.
Other Name: SMART
Active Comparator: Health
This group will receive the Brain Health Workshop educational program, twice a week for four weeks.
Behavioral: Brain Health Workshop
Brain Health Workshop provides information about brain health in a seminar format. Topics include: sleep, nutrition, and exercise.
- Improvement in memory or thinking after brain training [ Time Frame: beginning (0 weeks) to end (4 weeks) ]To examine short-term effects of treatment on cognition using neuropsychological measures
- Measures changes in brain wave activity [ Time Frame: beginning (0 weeks) and end (4 weeks) ]Electrophysiological responses will be recorded using event related potential to monitor responses to yes/no stimuli.
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): NCT02588209
|United States, Texas|
|UTD Center for BrainHealth|
|Dallas, Texas, United States, 75235|
|Principal Investigator:||Sandra Chapman, PhD||Center for Brain Health, University of Texas at Dallas|