- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05472727
Comparison of Physical Fitness, Walking Speed, Reaction Time In Older Adults With and Without Mild Cognitive Impairment
July 22, 2022 updated by: Zeynep SAG, Dokuz Eylul University
The aim of the study is to compare physical fitness, walking speed and hand reaction time measurements in older adults with different cognition levels according to the Montreal Cognitive Assessment Scale (MOCA).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Zeynep sağ, PT
- Phone Number: +905347480112
- Email: fzt.zeynep.sag@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years and older (Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
elderly people who are healthy or with mild cognitive impairment
Description
Inclusion Criteria:
- Being 65 years or older
- Volunteering to participate in the study
- 10 meters independent walking
- Being diagnosed with mild cognitive dysfunction
- Not being diagnosed with cognitive dysfunction
- Having received five years of basic education
Exclusion Criteria:
- Having had an upper or lower extremity surgery in the last 6 months
- Having a health problem that prevents completing the tests in the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Case group (mild cognitive impairment)
geriatric population with mild cognitive impairment
|
Reaction time tests consist of 3 sub-parameters as simple reaction time, selective reaction time and distinctive reaction time.
Participants will do these tests on the computer.
The physical fitness test will be evaluated with the senior fitness test used for geriatrics and the 8 meter walking speed test.
|
|
Control Group (healthy elderly)
healthy older adults without cognitive impairment
|
Reaction time tests consist of 3 sub-parameters as simple reaction time, selective reaction time and distinctive reaction time.
Participants will do these tests on the computer.
The physical fitness test will be evaluated with the senior fitness test used for geriatrics and the 8 meter walking speed test.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
reaction time
Time Frame: Participants are expected to complete the 3 sub-parameters of reaction time measurements in an average of 20 minutes, including rest periods
|
reaction time
|
Participants are expected to complete the 3 sub-parameters of reaction time measurements in an average of 20 minutes, including rest periods
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
physical fitness
Time Frame: Physical fitness tests are expected to take an average of 20 minutes.
|
physical capacity of the person
|
Physical fitness tests are expected to take an average of 20 minutes.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ibrahim Engin Simsek, professor, iengin.simsek@gmail.com
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
August 1, 2022
Primary Completion (Anticipated)
January 1, 2023
Study Completion (Anticipated)
May 1, 2023
Study Registration Dates
First Submitted
July 22, 2022
First Submitted That Met QC Criteria
July 22, 2022
First Posted (Actual)
July 25, 2022
Study Record Updates
Last Update Posted (Actual)
July 25, 2022
Last Update Submitted That Met QC Criteria
July 22, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 6987-GOA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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