- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01236664
An Evaluation of the Memory at Work Program
October 11, 2011 updated by: Baycrest
With the aging of the Canadian population, older workers are accounting for more and more of the working-age population.
Despite recent interest in cognitive training, there are currently no validated programs that specifically target individuals in the work force.
The investigators will conduct a small-scale randomized controlled trial to test the effectiveness of the previously developed Memory at Work program.
The investigators will recruit 60 individuals and randomly assign them to the active intervention or a control intervention.
The investigators will examine outcomes related to knowledge, behavioral change, self-efficacy, objective memory, and workplace productivity.
The investigators expect larger improvements on these measures in the active relative to the control group.
Study Overview
Status
Withdrawn
Conditions
Intervention / Treatment
Detailed Description
This is a pre-test/post-test randomized controlled trial.
Participants who meet eligibility criteria will undergo baseline testing that involves completing questionnaires and objective cognitive tests.
Participants will then be randomly assigned (by coin toss) to the intervention or control group.
After participating in their respective workshops, both groups will undergo immediate post-testing and 1-month follow-up post testing.
After the final assessment, the control group will be given the opportunity to participate in the intervention workshop.
No further testing of this group will occur, as there will no longer be a comparable control group.
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M6A 2E1
- Baycrest
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
30 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Currently employed
- Between ages 30-65
- Fluent in English language
Exclusion Criteria:
- A severe head injury, epilepsy or other neurological disorder
- Currently unemployed
- Evidence of significant psychiatric disorder/use of psychotropic medications
- Evidence of substance abuse
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Memory Training
|
The Memory at Work program is a 4-hour classroom-based workshop that is led by a professional trainer.
The format of the program is experiential, with a heavy focus on discussion, self-discovery, and hands-on use of trained skills.
Specific memory compensation techniques are trained.
Training consists of an explanation of each technique (i.e., how and when to use it, the science behind the technique) and ample opportunities for hands-on use of the strategies.
Other Names:
|
Active Comparator: Control workshop
|
The control workshop consists of a 4-hour program that will train techniques for successfully completing Sudoku, word, and logic puzzles.
Like the experimental intervention, the control workshop will be engaging and challenging, and will involve a combination of individual and group activities.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Memory related knowledge and behaviour
Time Frame: 6 weeks
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Improved workplace productivity
Time Frame: 6 weeks
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Angela K. Troyer, PhD, Baycrest
- Principal Investigator: Kelly J Murphy, PhD, Baycrest
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Troyer AK, Rich JB. Psychometric properties of a new metamemory questionnaire for older adults. J Gerontol B Psychol Sci Soc Sci. 2002 Jan;57(1):P19-27. doi: 10.1093/geronb/57.1.p19.
- Troyer AK, Murphy KJ, Anderson ND, Moscovitch M, Craik FI. Changing everyday memory behaviour in amnestic mild cognitive impairment: a randomised controlled trial. Neuropsychol Rehabil. 2008 Jan;18(1):65-88. doi: 10.1080/09602010701409684.
- Troyer AK, Hafliger A, Cadieux MJ, Craik FI. Name and face learning in older adults: effects of level of processing, self-generation, and intention to learn. J Gerontol B Psychol Sci Soc Sci. 2006 Mar;61(2):P67-74. doi: 10.1093/geronb/61.2.p67.
- Troyer AK. Improving memory knowledge, satisfaction, and functioning via an education and intervention program for older adults. Aging, Neuropsychology, and Cognition 8, 256-268, 2001.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2012
Primary Completion (Anticipated)
January 1, 2013
Study Completion (Anticipated)
January 1, 2013
Study Registration Dates
First Submitted
November 8, 2010
First Submitted That Met QC Criteria
November 8, 2010
First Posted (Estimate)
November 9, 2010
Study Record Updates
Last Update Posted (Estimate)
October 12, 2011
Last Update Submitted That Met QC Criteria
October 11, 2011
Last Verified
October 1, 2011
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- REB1043
- HTX 10-43 (Other Grant/Funding Number: HTX)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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