Cognitive-Frailty Gait Biomechanics for Early Dementia Detection

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50+
SponsorUniversiti Sains Malaysia

About this trial

The purpose of this study is to better understand how physical characteristics, walking patterns, and a blood-based brain health marker differ between older adults with dementia and healthy older adults.

Dementia is often associated with changes in physical health and movement, but these changes are not fully understood. This study asks whether people with dementia show differences in body composition, walking ability, and levels of brain-derived neurotrophic factor (BDNF), a protein involved in brain function, compared with individuals without dementia.

To answer this question, participants will complete a single assessment session that includes basic physical measurements, an assessment of walking while moving at a comfortable pace, and a small blood sample collection. The information collected will be used to compare the two groups and explore possible relationships between physical function, walking patterns, and BDNF levels.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Older adults aged 50 years and above

Able to ambulate independently without the use of walking aids

Must be able to understand instructions, communicate effectively

Free from any acute or unstable medical conditions at the time of assessment.

Disqualifiers

Present with any diagnosed neurological disorder such as stroke or Parkinson's disease

History of psychiatric illness, including major depressive disorder.

Individuals with uncontrolled cardiovascular, metabolic, or endocrine conditions

Have significant visual, auditory, or musculoskeletal impairments that may influence gait performance

Trial population

USM memory clinic

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

60 Participants
are grouped into 2 trial groups
Group A: MCI group
Group B: Healthy control group

Trial outcomes

Primary outcomes

1

Gait speed during normal walking

Average gait speed measured during normal walking using motion capture analysis. Unit of Measure: Meters per second (m/s)

Time frame
At baseline (single assessment)
2

Stride length during normal walking

Mean stride length measured during normal walking using motion capture analysis. Unit of Measure: Meters (m)

Time frame
At baseline
3

Cadence during normal walking

Cadence measured during normal walking using motion capture analysis. Unit of Measure: Steps per minute (steps/min)

Time frame
At baseline (single assessment)
4

Cognitive function assessed by the Montreal Cognitive Assessment (MoCA)

Global cognitive function measured using the Montreal Cognitive Assessment (MoCA), a standardized cognitive screening tool assessing multiple cognitive domains. Unit of Measure: Score on a scale Scale Description: Montreal Cognitive Assessment (MoCA) total score ranges from 0 to 30, with higher scores indicating better cognitive function.

Time frame
At baseline (single assessment)

Secondary outcomes

1

Handgrip strength

Maximum handgrip strength measured using a handheld dynamometer. Unit of Measure: Kilograms (kg)

Time frame
At baseline
2

Serum brain-derived neurotrophic factor (BDNF) concentration

Serum brain-derived neurotrophic factor (BDNF) concentration measured from blood samples. Unit of Measure: ng/mL

Time frame
At baseline
3

Functional mobility assessed by the Timed Up and Go test

Functional mobility measured using the Timed Up and Go (TUG) test, which assesses the time required to stand up from a chair, walk 3 meters, turn, return, and sit down. Unit of Measure: Seconds (s) Directionality: Lower values indicate better functional mobility.

Time frame
At baseline (single assessment)

Other outcomes

Sponsors and contacts

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