Efficacy of Cognitive Stimulation Therapy Integrated With Stress Reduction Intervention for Adults With Mild Cognitive Impairment
1 other identifier
interventional
12
0 countries
N/A
Brief Summary
The aim of this study is to determine if integrating a culturally congruent indigenous stress reduction intervention into Cognitive Stimulation Therapy (CST) enhances cognitive outcomes in Pakistani adults with Mild Cognitive Impairment (MCI).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2026
CompletedFirst Submitted
Initial submission to the registry
March 4, 2026
CompletedFirst Posted
Study publicly available on registry
March 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2026
March 13, 2026
March 1, 2026
3 months
March 4, 2026
March 10, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Change in Montreal Cognitive Assessment (MoCA) total score from baseline to 7 weeks
The Montreal Cognitive Assessment (MoCA) will be used to assess overall cognitive functioning, including attention, memory, language, executive functions, and visuospatial abilities. The MoCA total score ranges from 0 to 30, with higher scores indicating better cognitive functioning. Assessments will be conducted at baseline and after completion of the 7-week intervention period.
7 weeks
Study Arms (3)
Cognitive Stimulation Therapy integrated with Stress Reduction Intervention
EXPERIMENTALParticipants receive Cognitive Stimulation Therapy integrated with Stress Reduction Intervention for 7 weeks.
Cognitive Stimulation Therapy (CST)
ACTIVE COMPARATORParticipants receive Cognitive Stimulation Therapy sessions for 7 weeks.
Control Group
NO INTERVENTIONParticipants will not receive any structured therapy during the 7 week study period.
Interventions
Participants in this Arm will receive Cognitive Stimulation Therapy integrated with Stress Reduction Intervention for 7 weeks, combining structured cognitive exercises targeting memory, attention, and problem-solving with guided stress reduction techniques.
Participants in this Arm will attend Cognitive Stimulation Therapy sessions only for 7 weeks, including structured cognitive exercises targeting memory, attention, and problem-solving in a group format.
Eligibility Criteria
You may qualify if:
- Adults aged 45 years and above
- Individuals with education up to Matric
- Individuals who obtain a score lower than 23 on Montreal Cognitive Assessment (MoCA) suggesting the presence of cognitive decline.
- Individuals who obtain a score of 14 or more on the Perceived Stress Scale suggesting increased levels of perceived stress (moderate and high)
- Individuals who obtain score ranged from 13 to 25 (Poor to Adequate) on Quality of Life in Alzheimer's Disease (Qol-AD)
You may not qualify if:
- Diagnosis of dementia or major neurocognitive disorder
- Presence of severe psychiatric illness (e.g., psychosis, major depressive episode)
- Significant hearing or visual impairments that interfere with participation
- Currently undergoing psychological or cognitive therapy
- Any neurological condition that may interfere with cognitive assessment (e.g., stroke, Parkinson's disease)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Student
Study Record Dates
First Submitted
March 4, 2026
First Posted
March 13, 2026
Study Start
March 1, 2026
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Last Updated
March 13, 2026
Record last verified: 2026-03