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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05652140
Other study ID # PACNL_APOE_PROSPECTIVE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2018
Est. completion date May 1, 2021

Study information

Verified date February 2023
Source National Taiwan Normal University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The current research project aims to investigate the interaction of cardiorespiratory fitness (CRF) and the ApoE genotype with neurocognitive functions.


Description:

The current research project aims to investigate the interaction of cardiorespiratory fitness (CRF) and the ApoE genotype with neurocognitive functions. The three main purposes of the current research project seek to achieve: 1. An exploration of the associations of, as well as the interactions between, CRF assessed at the Baseline Stage, and the ApoE genotype, along with cognitive functions in cognitively healthy late-middle-aged older adults. 2. The employing of an event-related potential (ERP) to investigate the associations between the baseline CRF, the ApoE genotype, and cognitive functions in cognitively healthy late-middle-aged older adults, as well as the potential underlying neuroelectrical mechanisms. 3. An investigation of the interactions between the changes of CRFs assessed at the Baseline and the Follow-Up Stages and the ApoE genotype in relation to neurocognitive function, as well as the underlying neuroelectrical mechanisms, in cognitively healthy late-middle-aged older adults.


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date May 1, 2021
Est. primary completion date April 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria: - right handed - no history of cardiorespiratory disease - normal or corrected-to-normal vision based on the 20/20 standard - no risk of performing physical activities, as measured by the Physical Activity Readiness Questionnaire Exclusion Criteria: - the scores of Mini-Mental Status Examination (MMSE) < 25 and cognitively intact upon study entry - history of psychiatric or neurological diseases - color-blindness

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Data collections
Data collections of cognitive function, neuroelectrical activities, ApoE genotype, and physical fitness.

Locations

Country Name City State
Taiwan Department of Physical Education and Sport Sciences, National Taiwan Normal University Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan Normal University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in inhibitory performance: Stroop task Inhibitory performance was assessed using the computerized Stroop task at the baseline and at the follow-up assessments. Changes in inhibitory performance from Baseline to the Follow-Up Stages were assessed. 30 minutes each at the Baseline and the Follow-Up Stages.
Primary Changes in higher order executive performance: Tower of London Test Higher order executive performance was assessed using the Tower of London Test at the baseline and at the follow-up assessments. Changes in higher order executive performance from Baseline to the Follow-Up Stages were assessed. 25 minutes each at the Baseline and the Follow-Up Stages.
Primary Changes in neuroelectrical activities The neuroelectrical activities during the Stroop task were recorded and analyzed using the Neuroscan system. Changes in the neuroelectrical activities from Baseline to the Follow-Up Stages were assessed. 30 minutes each at the Baseline and the Follow-Up Stages.
Secondary ApoE genotype Based on the genetic biomarkers (rs429358 and rs7412), participants' ApoE genotype was determined. 5 minutes at the Baseline Stage.
Secondary Physical fitness measurements: Changes in aerobic fitness Participants' aerobic fitness was estimated using the submaximal cycle ergometer test at the baseline and at the follow-up assessments. Changes in aerobic fitness from Baseline to the Follow-Up Stages were assessed. 20 minutes each at the Baseline and the Follow-Up Stages.
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