NCT01708200

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
76

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2012

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2012

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

October 10, 2012

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 16, 2012

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2015

Completed
Last Updated

October 16, 2012

Status Verified

October 1, 2012

Enrollment Period

3 years

First QC Date

October 10, 2012

Last Update Submit

October 15, 2012

Conditions

Keywords

MemoryInterventionComputerizedPsychoeducationalMental Illness

Outcome Measures

Primary Outcomes (1)

  • Declarative Memory Measure - Hopkins Verbal Learning Test

    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.

    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).

Secondary Outcomes (1)

  • 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 Outcomes (1)

  • 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).

Study Arms (1)

Memory Intervention

EXPERIMENTAL

Two types of memory protocols (psychoeducational vs computerized) will be compared in a population of individuals with mental illness.

Other: Memory Intervention

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.

Memory Intervention

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

St. Joseph's Healthcare Hamilton

Hamilton, Ontario, L8N 3K7, Canada

Location

MeSH Terms

Conditions

Memory DisordersMental Disorders

Condition Hierarchy (Ancestors)

Neurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Bruno J Losier, Ph.D.

    St. Joseph's Healthcare Hamilton

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Bruno J Losier, Ph.D.

CONTACT

Michele Bridge

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Neuropsychologist

Study Record Dates

First Submitted

October 10, 2012

First Posted

October 16, 2012

Study Start

October 1, 2012

Primary Completion

October 1, 2015

Study Completion

October 1, 2015

Last Updated

October 16, 2012

Record last verified: 2012-10

Locations