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A Comparison of the Effectiveness of Two Types of Memory Training Programs in People With a Diagnosis of Mental Illness.

A Comparison of the Effectiveness of Two Types of Cognitive Training Interventions Administered to Individuals With a Diagnosis of a Mental Health Condition.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01708200
Enrollment
76
Registered
2012-10-16
Start date
2012-10-31
Completion date
2015-10-31
Last updated
2012-10-16

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

Conditions

Memory Impairment

Keywords

Memory, Intervention, Computerized, Psychoeducational, Mental Illness

Brief summary

This study will compare the effectiveness of a psychoeducational memory program versus a computerized memory program in individuals with mental illness. Although improvements are expected with both form of interventions, we do not know which will provide maximal benefit in this population.

Detailed description

The aim of the current study is to compare two memory strategies, a top-down (i.e., educational and interventional)protocol vs. a bottom-up (computerized)protocol, in a population of individuals diagnosed with mental illness. Performance on ecologically validated memory tasks will be measured before and after each intervention protocol. Improvements are expected following each protocol. However, there is no evidence available to support added benefits from one protocol over another. As such, the current study will endeavour to contrast the two intervention types (top-down vs. bottom-up) to determine which, if any, provides maximal benefit.

Interventions

A comparison of two type of memory intervention protocols; a psychoeducational/intervention protocol versus a computerized memory protocol in a population of individuals with mental illness.

Sponsors

St. Joseph's Healthcare Hamilton
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Memory impairment equivalent to 1.5 std. dev. below average for age * Speak and read English fluently

Exclusion criteria

* Older than 65 years of age * Significant visual impairment (e.g., cataracts, macular degeneration) * Motor impairment (e.g., hemiplegia on dominant side) * Diagnosis of Dementia * Alcohol and/or substance abuse (in past 3 months)

Design outcomes

Primary

MeasureTime frameDescription
Declarative Memory Measure - Hopkins Verbal Learning TestParticipants will be asked to complete this measure prior to the start of the intervention and again at the completion of the intervention (i.e., interval of 5 weeks between pre and post measurements).Individuals participating in either protocol (i.e., top-down or bottom-up) will complete the memory measure before the commencement of the treatment and again at the end of treatment.

Secondary

MeasureTime frame
Mood Measure - Depression Anxiety Stress Scale (Lovibond & Lovibond, 1993)Participants will be asked to complete this measure prior to the start of the intervention and again at the completion of the intervention (i.e., interval of 5 weeks between pre and post measurements).

Other

MeasureTime frame
Functional - Multifactorial Metamemory Questionnaire (Troyer & Rich, 2011)Participants will be asked to complete this measure prior to the start of the intervention and again at the completion of the intervention (i.e., interval of 5 weeks between pre and post measurements).

Countries

Canada

Contacts

Primary ContactBruno J Losier, Ph.D.
losierb@stjoes.ca(905) 522-1155
Backup ContactMichele Bridge
(905) 522-1155

Outcome results

None listed

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