CClinicalTrials.gg
WithdrawnNCT01236664Updated Oct 12, 2011

An Evaluation of the Memory at Work Program

An interventional study of Memory training and Control Workshop in Cognition - Other and Ageing, sponsored by Baycrest. Withdrawn at 1 site in Canada. Open to participants aged 30 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-10-12.

Sponsored by Baycrest · Not applicable, Interventional, and Treatment

Why this study was withdrawn
The sponsor is no longer developing this program and therefore has withdrawn the funding.
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
30 Years to 65 Years
Sex
All
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Study summary

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.

Read the 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.

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Conditions studied

  • Cognition - Other
  • Ageing

Keywords

  • memory training
  • mnemonics
  • cognition
  • work
03

In context

Lead sponsor

Baycrest is the lead sponsor of 33 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Currently employed
  • Between ages 30-65
  • Fluent in English language

Exclusion criteria

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Memory Training

    Behavioral: Memory training

  • Active comparator
    Control workshop

    Behavioral: Control Workshop

Interventions

  • BehavioralMemory 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.

    Also known as: Memory at Work Program

  • BehavioralControl 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.

06

What researchers measure

Primary outcomes

  1. Memory related knowledge and behaviour

    Time frame: 6 weeks

Secondary outcomes

  1. Improved workplace productivity

    Time frame: 6 weeks

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Study locations

1 site
  • Baycrest
    Toronto, Ontario M6A 2E1, Canada
08

References and documents

Publications

  • 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. PubMed 17943615 ↗
  • 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. PubMed 16497956 ↗
  • 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. PubMed 11773220 ↗
  • 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.
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01236664
Lead sponsor
Baycrest
Collaborators
Cogniciti Inc.
First posted
Nov 9, 2010
Start date
Jan 2012
Primary completion
Jan 2013 (estimated)
Completion
Jan 2013 (estimated)
Last update
Oct 12, 2011

Study contacts

Angela K. Troyer, PhD
principal investigator · Baycrest
Kelly J Murphy, PhD
principal investigator · Baycrest

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Oct 2011. You cannot join it, but the record below documents what was studied.

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