MedPath

Effects of Visual Art Training on Dementia

Not Applicable
Completed
Conditions
Dementia
Interventions
Behavioral: Visual Arts Training
Registration Number
NCT03175822
Lead Sponsor
York University
Brief Summary

The purpose of the proposed study is to better understand what benefits visual art has on reducing problematic symptoms in dementia patients, including those with Alzheimer's disease.

Detailed Description

Participants:

Participants will be residents, attendees and/or members of assisted living locations and/or dementia (or related) day programs. There will be two groups: an art training group and a waitlist control group.

Data Analysis:

1. For primary measures, t-tests on pre-post difference scores comparing art training and waitlist groups.

2. For possible confounding effects, tests for confounds related to background factors (socioeconomic status, education level, gender, activity participation).

Procedure:

A randomized controlled trial design will be utilized to assess two groups of dementia patients: an art training experimental group and a structured usual-activity waitlist control group. The experimental group will participate in a visual art training program and the waitlist control group will participate in their usual structured group activities. The waitlist control group will receive the art training program once post-testing is complete. Before, during, and/or after the art programs and/or control activities, participants will be observed and complete assessments.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
83
Inclusion Criteria
  • Dementia
Exclusion Criteria
  • Inability to participate in the art training program due to physical or cognitive limitations

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Visual Arts TrainingVisual Arts TrainingVisual Arts Training
Primary Outcome Measures
NameTimeMethod
Change in cognitionbaseline up to three weeks prior, and final assessment one to two weeks post-intervention

Montreal Cognitive Assessment (MoCA; Nasreddine, 2005)

Change in visual working memorybaseline up to three weeks prior, and final assessment one to two weeks post-intervention

Body Part Pointing Test (Stopford et al., 2010)

Change in auditory working memorybaseline up to three weeks prior, and final assessment one to two weeks post-intervention

Digit Span (Weschler, 2008)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Alzheimer's Society of York Region

🇨🇦

Aurora, Ontario, Canada

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