Skip to content

Effects of Cognitive Intervention for Older Adults With Memory Decline: A Pilot Study

Effects of Cognitive Intervention for Older Adults With Memory Decline: A Pilot Study

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00609427
Enrollment
30
Registered
2008-02-07
Start date
2008-05-31
Completion date
2010-05-31
Last updated
2010-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Impairment

Keywords

cognitive training, cognitive rehabilitation

Brief summary

The purpose of this study is to evaluate the effects of training in memory skills vs. use of external memory aids on everyday memory functioning in older people with mild cognitive impairment.

Detailed description

Some older people experience memory loss that is worse than other people of their age, although they are not demented. This condition is known as mild cognitive impairment (MCI). Healthy older people can learn mnemonic strategies to improve their memory abilities. Can cognitive rehabilitation help people with MCI do better on mental tasks or maintain better functioning in everyday life? This study will evaluate the effects of two different rehabilitation programmes. Patients in the memory training group will learn mental strategies aimed at improving memory. Patients in the memory compensation group will learn to use external memory aids.

Interventions

BEHAVIORALMEMO programme (Inst Universitaire de Geriatrie, Montreal)

8 weekly group training sessions in mnemonic strategies, administered by clinical psychologist.

BEHAVIORALExternal memory aids training

8 weekly group sessions of training in the use of external memory aids, administered by clinical psychologist

Sponsors

McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of mild cognitive impairment

Exclusion criteria

* Unable to speak and understand English * Unable to comply with treatment program due to significant comorbid illness; OR * Anticipated inability to attend all study sessions

Design outcomes

Primary

MeasureTime frame
Rey Auditory Verbal Learning Test19-20 weeks
Wechsler Memory Scale - Logical Memory19-20 weeks
Face-name associations test19-20 weeks
Multifactorial Memory Questionnaire - Ability subscale19-20 weeks

Secondary

MeasureTime frame
Digit Span (non-memory test)19-20 weeks
Rivermead Behavioural Memory Test19-20 weeks
Multifactorial Memory Questionnaire - Strategies and Contentment subscales19-20 weeks
FAS test (non-memory)19-20 weeks
Category fluency (non-memory test)19-20 weeks
Victoria Stroop Test (non-memory test)19-20 weeks

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026