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Effect of Art Therapy on Cognitive and Hand Functions of Alzheimer's Patients

NCT07163377 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-09
Last updated
2025-09-09

Condition(s) studied

Alzheimer Disease

Investigational drug(s) / intervention(s)

Experimental Group

Experimental Group: Participants in the intervention group will undergo art therapy sessions

Study summary

This randomized controlled trial aims to investigate the effects of art therapy on cognitive functions and hand functions in individuals with Alzheimer's disease. Alzheimer's disease is a progressive neurodegenerative disorder characterized by decline in memory, executive functions, and daily living activities. In addition, fine motor skills and hand-eye coordination are significantly impaired, limiting independence in daily tasks.

Art therapy is a non-pharmacological, low-cost, and feasible intervention that involves creative activities such as mandala painting, collage, clay modeling, and drawing. It has been shown to support cognitive performance, emotional well-being, and motor coordination by stimulating neuroplasticity. However, evidence focusing specifically on its impact on hand function in Alzheimer's patients remains limited.

In this study, 50 participants aged 60 years and older with mild to moderate Alzheimer's disease will be randomly assigned to an intervention group or a control group. The intervention group will attend art therapy sessions twice a week for 8 weeks (60 minutes per session), while the control group will receive no intervention. Cognitive functions will be assessed using the Mini-Mental State Examination (MMSE), and hand functions will be evaluated with the Nine Hole Peg Test (NHPT) and surface electromyography (sEMG) of forearm muscles.

The results of this study are expected to provide valuable evidence on the role of art therapy in supporting both cognitive and motor rehabilitation in Alzheimer's disease, potentially contributing to improved daily living independence and quality of life.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Being 60 years of age or older * Having a diagnosis of mild or moderate Alzheimer's disease * Possessing the physical and cognitive capacity to participate in art therapy interventions * Providing informed consent Exclusion Criteria: * Being in the severe stage of Alzheimer's disease * Having a history of severe psychiatric disorders such as schizophrenia or major depression * Having a physical disability that prevents the use of the upper extremities * Being unable to participate in the intervention due to visual or hearing impairments

Primary outcome measure(s)

  • Mini-Mental State Examination — From enrollment to the end of treatment at 8 weeks
    The Mini-Mental State Examination (MMSE) is a standardized test developed to assess the overall level of cognitive functioning in individuals. It is brief and easy to administer. The test consists of 11 items covering various cognitive domains, including orientation to time and place, short-term memory, attention and calculation, recall, language skills, and visuospatial abilities. The total score is 30; lower scores indicate cognitive impairment. In general, scores of 24 or below suggest the need for clinical attention regarding cognitive dysfunction.
  • Surface Electromyography (sEMG) — From enrollment to the end of treatment at 8 weeks
    The Mini-Mental State Examination (MMSE) is a brief, standardized instrument designed to evaluate global cognitive functioning in individuals. It can be administered in a short period of time and assesses 11 domains, including orientation to time and place, short-term memory, attention and calculation, recall, language abilities, and visuospatial skills. The maximum score is 30, with lower scores reflecting greater levels of cognitive impairment. A threshold score of 24 or below is generally considered indicative of clinically significant cognitive dysfunction warranting further evaluation.

Trial sites (1)

FacilityCityRegionStatus
Fenerbahçe Üniversitesi Ataşehir Istanbul
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07163377 on ClinicalTrials.gov ↗ ← All trials in Turkey