MedPath

Visual Arts Interventions With Older Adults

Not Applicable
Not yet recruiting
Conditions
Feasibility Study
Registration Number
NCT06645652
Lead Sponsor
Northeastern University
Brief Summary

The present study investigates the feasibility, acceptability, and preliminary effects of a novel visual arts-based intervention in an older adult population. In a randomized controlled design, two arts-based interventions will be evaluated with a group of 50 participants.

Detailed Description

A two-arm randomized controlled study will be conducted to obtain within-group ratings of feasibility and acceptability, as well as between-group differences in drawing skills after training. In the drawing intervention, participants will learn and train drawing skills through exercises that target attention, perception, and visuospatial reasoning. In the active control condition, participants will navigate virtual art galleries. Both interventions will be completed remotely and at home. Participants will complete in-lab assessment sessions before and after the training.

Each intervention consists of 6 weeks of training for up to 2 hours a week, including up to 1 hour of a self-guided lesson and prompted daily drawing practice adding up to 1 hour in the drawing intervention and 2 1-hour sessions of virtual gallery exploring per week in the arts appreciation intervention. The pre-test is administered within one week of the start of training and the post-test is administered within one week of training completion.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • 55-85 years of age
  • Able to understand and speak English and follow study procedures
  • Does not have a psychological or neurological condition that would prevent from being able to give consent to participate
  • Less than 2 years of formal visual arts training
Exclusion Criteria
  • Formal diagnosis of dementia or other neurological disease, including Mild Cognitive Impairment
  • A final score below 17 on the Montreal Cognitive Assessment - Blind (phone) version
  • Abnormal visual acuity prohibitive of tablet-based training
  • Physical handicap (motor or perceptual) that would impede training procedures
  • Medical illness requiring treatment and/or significant absences during the study timeline

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Feasibility - completion rateThroughout training and post-test 6-8 weeks later

% of participants who completed both testing sessions

Feasibility - adherenceThroughout training and post-test 6-8 weeks later

% of lessons that participants completed, from 0-6

Feasibility - frequencyThroughout training and post-test 6-8 weeks later

Frequency: times a week that participants completed training, 0-7 for days practiced each week

Feasibility - attritionThroughout training and post-test 6-8 weeks later

Attrition reason: participants withdrawing will select from one of 5 options or 'other' to record the reason for withdrawing

Acceptability - valueThroughout training and post-test 6-8 weeks later

Perceived value of the course content, likert scale 1-5

Acceptability - clarityThroughout training and post-test 6-8 weeks later

Perceived clarity on the course content, likert scale 1-5

Acceptability - engagementThroughout training and post-test 6-8 weeks later

Level of engagement with the course materials, likert scale 1-5

Change in Drawing skillsPre-test (baseline) and post-test 6-8 weeks later

Participants will have 5 minutes to draw a photograph. Accuracy is scored using two methods: angle error at defined points of intersection and a rubric assessing accuracy on global and local features. Both ratings are averaged into a composite z-score, as well as looked at separately.

Secondary Outcome Measures
NameTimeMethod
Change in Perception - contour integrationPre-test (baseline) and post-test 6-8 weeks later

Participants tap on circles of aligned Gabors embedded in a scene of randomly oriented Gabors. A circle will be present for 3 seconds and switch to the next trial if it is not seen. Number of circles spotted, reaction times on spotted circle, and lowest level of alignment will be recorded. Z-scores will be calculated.

Change in Perception - visual disembeddingPre-test (baseline) and post-test 6-8 weeks later

Participants search for a target shape in 3 complex gestalts of overlapping shapes. Participants select the complex shape containing the target. Response times and accuracy are measured. Z-scores will be calculated.

Change in Visuospatial Reasoning - construction and memoryPre-test (baseline) and post-test 6-8 weeks later

Complex Figures Copy and Recall will assess visuospatial construction and memory (10 min). Participants will complete three sets of drawing complex shapes from observation and memory after a block of word learning. Accuracy will be scored using a validated rubric.

Change in Visuospatial Reasoning - mental transformationPre-test (baseline) and post-test 6-8 weeks later

3D Mental Rotation (3 min) will test mental transformation. Participants will be briefly shown two figures and asked to determine whether the figures are the same or mirror reversed. Mean and SD reaction time per angular disparity and errors per angular disparity will be extracted.

Change in AttentionPre-test (baseline) and post-test 6-8 weeks later

A Rule switch task will measure set shifting. Participants will sort shapes by color or shape. Performance will be calculated as the response times on accurate switch trials.

Change in MindfulnessPre-test (baseline) and post-test 6-8 weeks later

Participants complete a version Solloway Mindfulness Survey adapted to drawing. The questionnaire includes 30 questions on a 7-point scale on the degree to which engaging in drawing is related to different aspects of mindful attention.

Change in Mental WellbeingPre-test (baseline) and post-test 6-8 weeks later

Mental Wellbeing is assessed by the WEMWBS, which includes 14 questions on a 5 point scale about positive mental wellbeing.

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