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Effects of Wearable Sensor-based Interactive Cognitive-motor Training in Older Adults.

Not Applicable
Completed
Conditions
Subjective Memory Decline
Cognition Disorders in Old Age
Cognitive Decline, Mild
Interventions
Behavioral: cognitive-motor training
Behavioral: cognition training
Registration Number
NCT05983913
Lead Sponsor
Sahmyook University
Brief Summary

* Based on research showing that cognitive-motor training programs help improve cognition in older adults with mild cognitive impairment, this program uses an interactive system to combine cognitive training with exercise.

* The interactive system consists of wearable sensors and has the advantage of cognitive training without space constraints, and the cognitive training program consists of a total of five developed cognitive training games.

* The program is expected to improve the cognitive abilities of the elderly and improve their physical abilities.

Detailed Description

The proposed study will conduct a randomized controlled trial to compare the effects of a cognitive-motor training program using a wearable sensor-based interactive system on the cognitive and physical abilities of older adults in the community. Study participants will be randomly assigned to receive one of two interventions: (a) motor-cognitive training (b) cognitive training. All interventions will last 50 minutes and will be delivered twice a week for 6 weeks. To determine the effectiveness of the interventions, the primary outcome will assess PFC activity and cognition, and the secondary outcome will assess aerobic capacity, balance, upper extremity muscle strength, lower extremity muscle strength, and instrumental activities of daily living tasks. All assessments will be administered one week before and one week after the intervention.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Community-dwelling seniors age 65 and older
  • MMSE-K 18 or less
Exclusion Criteria
  • People of Hospitalized or institutionalized
  • People diagnosed with Alzheimer's disease
  • People diagnosed with vascular dementia
  • People with musculoskeletal conditions that make physical activity difficult
  • People with dizziness that makes physical activity difficult
  • People with a wound or bleeding in the head

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
cognitive-motor training groupcognitive-motor trainingParticipants will receive 50 minutes of cognitive-motor training twice per week for 6 weeks. The cognitive-motor training program uses a wearable sensor-based interactive system to perform cognitive tasks in a large space without the constraints of physical movement. Participants wear a wearable sensor-based device on their dominant arm or leg and use an interactive system to perform cognitive-motor tasks.
cognition training groupcognition trainingParticipants will receive 50 minutes of cognitive training twice a week for 6 weeks. The cognitive training program will be delivered in booklet form, and participants will perform the cognitive tasks of the cognitive-motor training in a seated position with no physical movement.
Primary Outcome Measures
NameTimeMethod
Change in prefrontal cortex activationchange from baseline to 6 week post intervention

Activation of the prefrontal cortex will be assessed by changes in HbO, and differences in PFC activity will be identified during cognitive tasks (memory, attention, and visuospatial cognition) before and after the assessment.

Change in cognitionchange from baseline to 6 week post intervention

For cognitive assessment, we will use the Montreal Cognitive Assessment (MoCA). The MoCA is a cognitive assessment tool used to identify MCI that assesses multiple cognitive domains, including memory, attention, language, visuospatial skills, executive function, and orientation to time and place.

Secondary Outcome Measures
NameTimeMethod
Change in upper extremity strengthenchange from baseline to 6 week post intervention

Upper extremity strength is assessed with the arm curl test. On women perform a biceps curl with a 2.3 kg dumbbell and men with a 3.6 kg dumbbell. They are seated in a chair with no armrests or backrest. Scoring is based on the number of repetitions performed in 30 seconds.

Change in grip strengthenchange from baseline to 6 week post intervention

Grip strength is measured using a dynamometer and the subject is seated in a chair with arms extended, natural rotation, elbow flexed 90 degrees, forearm at natural angle and wrist in dorsiflexion between 0 and 30 degrees. The subject is then asked to grip the dynamometer for 3 seconds and the average value (kg) over 3 trials is recorded.

Change in dynamic balance function 2change from baseline to 6 week post intervention

Dynamic balance is assessed using the Functional Reach Test (FRT). The FRT measures the distance (in centimeters) that the head of the third metacarpal of the hand moves by extending the arm forward without moving the foot from a standing position.

Change in Aerobic capacitychange from baseline to 6 week post intervention

Aerobic capacity is measured using the 6-minute walk test (6MWT). The 6MWT measures the distance a subject can walk in six minutes. You can take as many breaks as you like and the examiner can provide a chair. The examiner records the distance you walk in six minutes, the number of breaks you take, and the duration of the breaks.

Change in static balance functionchange from baseline to 6 week post intervention

To assess static balance, using the Single Leg Stance Test (SLS). The SLS measures the number of seconds standing on one leg with hands on hips and eyes open.

Change in dynamic balance function 1change from baseline to 6 week post intervention

The Four Square Step Test (FSST) is used to assess dynamic balance ability. The FSST consists of stepping safely and as quickly as possible, without touching the sticks, over four sticks placed in a criss-cross configuration on the floor, and is scored by recording the time in seconds.

Change in lower extremity strengthenchange from baseline to 6 week post intervention

Lower extremity strength is assessed using the 5 sit to stand test (5xSST). The 5xSST measures the number of seconds a subject can go from sitting to standing and back to sitting five times, with the shorter the time, the better the strength.

Change in Instrumental Activity of Daily Living(IADLs)change from baseline to 6 week post intervention

IADLs require higher cognitive skills than basic activities of daily living, and IADLs can detect functional changes in the early stages of dementia. Instrumental IADLs are assessed using the Functional Activities Questionnaire (FAQ). The FAQ can differentiate between Mild cognitive impairment(MCI) and mild Alzheimer's disease(AD).

Trial Locations

Locations (1)

Mapo senior welfare center

🇰🇷

Seoul, Korea, Republic of

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