- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04877600
Dual Task Performance in Community Dwelling Older Adults
May 4, 2021 updated by: AYŞE ÜNAL, Pamukkale University
The Relationship Between Cognitive and Motor Functions, and Dual Task Performance in Community Dwelling Older Adults: Gender Differences
Dual task performances may be impaired with the impairment in motor performance and cognitive functions due to aging.
The aim of the present study is to investigate the gender differences in dual task performance.
A total of 82 community dwelling older adults (41 males and 41 females) aged between 65 and 75 years were included in the study.
Motor performance was evaluated with sit-to-stand test, the timed up and go test, 10 m walking test and cognitive functions were evaluated with Montreal Cognitive Assessment Test.
Dual task performances were evaluated as motor-motor and cognitive-motor performance.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
82
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Denizli, Turkey
- Pamukkale University
-
-
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 to 75 years (OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Dual task performances may be impaired with the impairment in motor performance and cognitive functions due to aging.
Because of this, we aimed to investigate the gender differences in dual task performance.
Description
Inclusion Criteria:
- The individuals aged between 65 and 75 years, who agreed for participation, who received 8 or higher points from Hodkinson Mental test, who had no neurologic/orthopedic problems that could affect balance and walking, or communication problem were included in the study.
Exclusion Criteria:
- The individuals who were using 3 or more medications that could affect motor and cognitive functions, and the ones who could not complete the tests were excluded.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
gender difference
dual task performance
|
dual task performance measurement
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dual Task Performance
Time Frame: 5 minutes
|
Assessment of Dual Task Performance
|
5 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Montreal Cognitive Assessment Scale
Time Frame: 5 minutes
|
Assessment of Cognitive Functions
|
5 minutes
|
Timed Up and Go
Time Frame: 5 minutes
|
Assessment of Physical Performance
|
5 minutes
|
30 Seconds Sit-to-Stand Test
Time Frame: 5 minutes
|
Assessment of Physical Performance
|
5 minutes
|
10 Meter Walking Test
Time Frame: 5 minutes
|
Assessment of Physical Performance
|
5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (ACTUAL)
December 1, 2020
Primary Completion (ACTUAL)
March 1, 2021
Study Completion (ACTUAL)
April 1, 2021
Study Registration Dates
First Submitted
May 4, 2021
First Submitted That Met QC Criteria
May 4, 2021
First Posted (ACTUAL)
May 7, 2021
Study Record Updates
Last Update Posted (ACTUAL)
May 7, 2021
Last Update Submitted That Met QC Criteria
May 4, 2021
Last Verified
May 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 60116787-020/77265
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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