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Clinical Trials/NCT05983913
NCT05983913
Completed
Not Applicable

Effects of Cognitive-motor Training Using a Wearable Sensor-based Interactive System on Cognitive and Motor Performance in Older Adults.

Sahmyook University1 site in 1 country40 target enrollmentAugust 26, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cognitive Decline, Mild
Sponsor
Sahmyook University
Enrollment
40
Locations
1
Primary Endpoint
Change in prefrontal cortex activation
Status
Completed
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 26, 2023
End Date
October 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jihye Jung

Physical Therapist

Sahmyook University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change in prefrontal cortex activation

Time Frame: change 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 cognition

Time Frame: change 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 Outcomes

  • Change in upper extremity strengthen(change from baseline to 6 week post intervention)
  • Change in grip strengthen(change from baseline to 6 week post intervention)
  • Change in dynamic balance function 2(change from baseline to 6 week post intervention)
  • Change in Aerobic capacity(change from baseline to 6 week post intervention)
  • Change in static balance function(change from baseline to 6 week post intervention)
  • Change in dynamic balance function 1(change from baseline to 6 week post intervention)
  • Change in lower extremity strengthen(change from baseline to 6 week post intervention)
  • Change in Instrumental Activity of Daily Living(IADLs)(change from baseline to 6 week post intervention)

Study Sites (1)

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