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Developing a Drawing Therapy Intervention for Negative Emotions in Older Adults with Mild Cognitive Impairment Based on the PERMA Framework

Developing a Drawing Therapy Intervention for Negative Emotions in Older Adults with Mild Cognitive Impairment Based on the PERMA Framework

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125351
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Mild cognitive impairment

Interventions

Control group:Usual care
Test team:Painting therapy

Sponsors

Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=60 years; 2.Meeting the diagnostic criteria of the MCI International Working Group: (1) No pathological dementia but abnormal cognitive function; (2) Patients report or caregivers indicate cognitive impairment (this study used the MoCA Beijing version, with the optimal diagnostic cutoff scores being illiteracy 14 points across 14 items defined as ADL impairment; a total score >6 points on the BADL scale defined as BADL impairment; and a total score >8 points on the IADL scale defined as IADL impairment); 3. Hamilton Depression Rating Scale score >=7 and Hamilton Anxiety Rating Scale score >=7; 4. Voluntary participation by the individual or their caregiver with signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with severe somatic diseases, such as advanced cancer, acute phase of heart failure, or dialysis-stage renal failure, or psychiatric disorders, such as major depressive episode or acute phase of schizophrenia; or those with severe impairments in hand function, vision, or hearing that hinder participation; 2. Patients expected to leave the institution within the next 6 months or those in the terminal stage of life.

Design outcomes

Primary

MeasureTime frame
Cognitive function;Depression level;Anxiety level;

Secondary

MeasureTime frame
Activity of daily living;

Countries

China

Contacts

Public ContactChen Yanhua

Affiliated Hospital of Southwest Medical University

chen_yanhua25@163.com+86 189 8276 5016

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026