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Arch Support Effects on Balance and Gait in Older Adults With Mild Cognitive Impairment

N

National Taipei University of Nursing and Health Sciences

Status

Enrolling

Conditions

Mild Cognitive Impairment

Treatments

Device: arch support insoles (FootDisc)

Study type

Interventional

Funder types

Other

Identifiers

NCT05470062
CTH-110-2-5-018

Details and patient eligibility

About

This study aims to explore the effects of arch support insoles on balance and gait performance in older adults with mild cognitive impairment (MCI). We will recruit 40 female older adults with MCI. A randomized crossover trial will be used to determine the immediate effect of arch support insoles. All participants received one assessment session wearing and one session not wearing insole in a random order within 1-day. Then participants will be randomly allocated to experimental group (arch support insoles, n=20) or control group (no insoles, n=20) for at least 4-h every day for 1-month. Our primary outcomes include static standing balance, timed-up-and-go test, 10-m obstacle crossing, functional reach test, Short Physical Performance Battery (SPPB), and gait assessment during single- and dual-task walking for 20 m at self-selected comfortable pace while performing serial subtractions (cognitive interference) or carrying a tray (motor interference). Assessments will be conducted at baseline and after 2-wk and 4-wk of insole wear. Statistical analyses will be performed using SPSS 21.0 software. Two-way mixed ANOVA will be used to determine the immediate and short- and long-term effect of arch support insoles. The results of the current study are expected to provide evidences in supporting the use of arch support insoles for improving gait performance and postural stability for older adults with MCI which will contribute to balance and gait training as well as fall prevention.

Enrollment

40 estimated patients

Sex

Female

Ages

65 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • (1) female aged 65 years and over; (2) able to walk more than 20 m without walking aids; (3) had a Montreal Cognitive Assessment (MoCA) score lower than 26 ; (4) had self-reported memory complaints; and (5) had the ability to perform ADLs.

Exclusion criteria

  • (1) dementia; (2) a history of malignant tumors ; (3) the presence of an unstable neurological or orthopedic disease, or visual problems interfering with participation in the study; and (4) an education level less than 6 years (elementary school).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

experimental group
Experimental group
Description:
wear the insoles for at least 4-h every day for 1-month
Treatment:
Device: arch support insoles (FootDisc)
control group
No Intervention group
Description:
not wear insoles for at least 4-h every day for 1-month

Trial contacts and locations

1

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Central trial contact

Chen-Yi Song

Data sourced from clinicaltrials.gov

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