- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07415382
Frailty, Dual-Task Performance, and Activities of Daily Living in Older Adults
February 12, 2026 updated by: Hasan Gerçek, KTO Karatay University
The Relationship Between Frailty, Dual-Task Performance, and Activities of Daily Living in Older Adults
This study aims to examine the relationship between dual task performance, frailty level, and activities of daily living in older adults.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
200
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: Hasan Gerçek, P
- Phone Number: +905426488455
- Email: hasangercek42@gmail.com
Study Locations
-
-
Karatay
-
Konya, Karatay, Turkey (Türkiye), 42020
- Recruiting
- KTO Karatay University
-
Contact:
- Hasan Gerçek, PhD
- Phone Number: 05426488455
- Email: hasangercek42@gmail.com
-
Sub-Investigator:
- Gulfidan BASER, PhD
-
-
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
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Older Adults
Description
Inclusion Criteria:
- Be 65 years of age or older,
- Be literate
- Have a Mini Mental State Examination (MMSE) score of 24 or higher (cognitively sound)
- Be able to walk at least 10 meters without the use of assistive devices,
- Not have advanced sensory loss that impairs vision or hearing.
Exclusion Criteria:
- Having a severe neurological (Parkinson's, stroke, etc.) or orthopedic disorder,
- Having a psychiatric diagnosis that prevents communication.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Frailty
Time Frame: Baseline
|
Edmonton Frailty Scale: The scale was developed to measure frailty in older adults and is suitable for routine use by healthcare professionals without specialized training in geriatrics or gerontology.
The scale assesses a total of 17 points under 11 headings, including cognitive status, general health, dependency, social support, medication use, nutrition, mood, continence, and functional performance.
Fragility increases as the score rises
|
Baseline
|
|
Daily Living Activities
Time Frame: Baseline
|
The Katz Activities of Daily Living Index is the best known measure in clinical practice and the most widely used measure in clinical research.
This scale, which will be used to assess participants' level of independence in basic ADLs, includes 6 basic activities: bathing, dressing, toileting, transfers, continence, and eating.
Each activity is rated as independent (1 point) or dependent (0 points).
The total score ranges from 0 to 6. Higher scores mean greater independence.
|
Baseline
|
|
Dual Task Performance (Motor-Cognitive)
Time Frame: Baseline
|
Motor-Cognitive performance will be assessed using the Timed Up and Go test and motor-motor performance by carrying a tray with water-filled cups while walking.
|
Baseline
|
|
Dual Task Performance (Motor-Motor)
Time Frame: Baseline
|
Motor-motor performance by carrying a tray with water-filled cups while walking.
|
Baseline
|
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)
February 7, 2026
Primary Completion (Estimated)
June 13, 2026
Study Completion (Estimated)
June 30, 2026
Study Registration Dates
First Submitted
February 7, 2026
First Submitted That Met QC Criteria
February 12, 2026
First Posted (Actual)
February 17, 2026
Study Record Updates
Last Update Posted (Actual)
February 17, 2026
Last Update Submitted That Met QC Criteria
February 12, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- KaratayUH16
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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