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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05532371
Other study ID # Gazi University
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 30, 2019
Est. completion date February 1, 2020

Study information

Verified date September 2022
Source Mugla Sitki Koçman University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to demonstrate the effectiveness of the different combinations of exercises on the cognitive status of older adults with cognitive decline.


Description:

This study is planned to examine the effects of combined exercise on cognitive status, lower extremity muscle strength, mobility, physical performance, mood and quality of life in older adults with Mild Cognitive Impairment. Aerobic exercise training and lower limb (extremity) strengthening exercises were applied to the first group, dual-task training and lower limb strengthening exercises were applied to the second group, and aerobic exercise training, dual-task training and lower limb strengthening exercises were applied to the third group.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date February 1, 2020
Est. primary completion date December 1, 2019
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Not had a fall in the last six months. - Older adults with an mini mental state examination score between18-23. - Age = 65years. Exclusion Criteria: - having central nervous system pathology that will affect balance - diagnosed with vestibular pathology, - having deformities in the waist, hip, and knee joints, - having lower extremity amputation, - with lower extremity operation history, - malignancy affecting the lower extremity, - having moderate and severe congenital heart disease, coronary heart disease and cerebrovascular disease, - participants who cannot cooperate, - participants who use an assistive walking device, - participants having vision problems.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Aerobic exercise training combined with lower limb strengthening
The participants performed aerobic exercise training and lower limb strengthening during this intervention.
Dual-task training combined with lower limb strengthening group (DG)
The participants performed dual-task training combined with lower limb strengthening during this intervention.
Aerobic exercise training combined with dual-task training and lower limb strengthening
The participants performed aerobic exercise training combined with dual-task training and lower limb strengthening during this intervention.
Only lower limb strengthening group (CG)
The participants performed only lower limb strengthening group during this intervention.

Locations

Country Name City State
Turkey Gazi University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation Ankara

Sponsors (1)

Lead Sponsor Collaborator
Mugla Sitki Koçman University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mini-Mental State Examination Cognitive status examination is applied with a simple test called "Mini-Mental State Examination". 12 weeks
Primary Commander Power Track 2 Manual Tester Muscle strength strength is carried out with "Commander Power Track 2 Manual Tester". 12 weeks
Primary Timed Up and Go Test Functional mobility is evaluated by Timed Up and Go Test. 12 weeks
Primary Single Leg Stance Test Static balance is evaluated by Single Leg Stance Test 12 weeks
Primary Activities-specific Balance Confidence Scale Balance Confidence is evaluated by Activities-specific Balance Confidence Scale. 12 weeks
Primary Six-Minute Walk Test Exercise capacity is evaluated by Six-Minute Walk Test. 12 weeks
Primary Short Physical Performance Battery Physical performance is evaluated by Short Physical Performance Battery. 12 weeks
Primary Hamilton Depression Rating Scale Emotional status is evaluated by Hamilton Depression Rating Scale 12 weeks
Primary World Health Organization Quality of Life-Old module Quality of life is evaluated by World Health Organization Quality of Life-Old module 12 weeks
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