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THE EFFECT OF COGNITIVE STIMULATION PROGRAM ON COGNITION AND QUALITY OF LIFE IN THAI OLDER ADULTS WITH MILD COGNITIVE IMPAIRMENT

THE EFFECT OF COGNITIVE STIMULATION PROGRAM ON COGNITION AND QUALITY OF LIFE IN THAI OLDER ADULTS WITH MILD COGNITIVE IMPAIRMENT

Status
Unknown
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240713002
Enrollment
62
Registered
2024-07-13
Start date
2024-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Mild Cognitive Impairment Older Adults Mild Cognitive Impairment Cognitive Stimulation Program Cognition Quality of Life

Interventions

Cognitive Stimulation Program 8 weeks, once a week for 60 minutes ,waiting list control group and treatment as usual
Experimental Other,No Intervention No treatment
Cognitive Stimulation Program ,Control group

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Mild cognitive impairment as assessed by the Montreal Cognitive Assessment (MoCA) Thai version, with a cut-off score between 18 and 25. 2. Absence of depression as assessed by the Thai Geriatric Depression Scale: TGDS-15, with a cut-off score of less than 6. 3. Proficiency in reading and writing Thai without hindrance to research participation. 4. No physical conditions that would impede participation in the research. 5. No participation in cognitive stimulation programs in the past 6 months, or participation in such programs for no more than one continuous week, such as brain training groups or elderly clubs. 6. Willingness to cooperate in the research with a participation rate exceeding 80%. 7. Capability to provide informed consent independently.

Exclusion criteria

Exclusion criteria: Presence of physical or psychiatric conditions that impede participation in the research.

Design outcomes

Primary

MeasureTime frame
Cognition Pre-test at week 0 (during 1 week before intervention), Post-test at week 8 (during 1 week after intervention) Neuropsychological test

Secondary

MeasureTime frame
Quality of life Pre-test at week 0 (during 1 week before intervention), Post-test at week 8 (during 1 week after intervention) The Quality of Life-Alzheimer's Disease (QOL-AD)

Countries

Thailand

Contacts

Public ContactPhenphichcha Chuchuen

Chulalongkorn University

phenphichcha.psyche@gmail.com0613654955

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026