- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07562919
Comparison of Physical Performance, Balance, and Functional Mobility Parameters According to Walking Speed in Geriatric Individuals
April 25, 2026 updated by: Gulfidan Tokgoz, Istanbul University - Cerrahpasa
Comparison of Physical Performance, Balance, and Functional Mobility Parameters According to Walking Speed Threshold Values in Geriatric Individuals
The aim of this study is to examine the determining role of walking speed on physical performance parameters in individuals aged 65 and over.
The study aims to compare flexibility, lower extremity muscle strength (5-count sit-stand test), static balance (single-leg balance), upper extremity muscle strength (hand grip), dynamic balance (FUT), functional mobility (TUG), and stair climbing/climbing skills in individuals with walking speeds of 0.4-0.8
m/s (limited community mobility) and above 0.8 m/s (independent community mobility).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Although the relationships between walking speed and individual physical parameters have been studied in the geriatric literature, comprehensive analyses comparing multidimensional parameters such as flexibility, static-dynamic balance, hand grip strength, and stair activity performance in groups separated according to walking speed threshold values (0.4-0.8 m/s and >0.8 m/s) are needed.
This study aims to identify which physical components show the most significant deficits when walking speed decreases, thereby providing a scientific basis for clinical assessment processes and personalized preventive rehabilitation programs.
Study Type
Observational
Enrollment (Estimated)
76
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: GULFİDAN TOKGÖZ, Lecturer, PhD (c)
- Phone Number: 0552 022 76 32
- Email: gulfidan.tokgoz@gmail.com
Study Locations
-
-
-
Balıkesir, Turkey (Türkiye)
- Balıkesir University
-
Contact:
- GULFİDAN TOKGÖZ, Lecturer, PhD (c)
- Phone Number: 0552 022 76 32
- Email: gulfidan.tokgoz@gmail.com
-
Sub-Investigator:
- Bilal Katipoğlu, Assoc. Prof. Dr.
-
Contact:
- Nilay ARMAN, Assoc. Prof. Dr.
- Phone Number: +905534558707
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Sub-Investigator:
- Saime Nilay Arman, Assoc. Prof. Dr.
-
-
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
Geriatric individuals aged 65 and over who meet the inclusion criteria for the study.
Description
Inclusion Criteria:
- Being 65 years of age or older
- Being able to perform walking functions
- Having sufficient mobility to perform the physical performance tests included in the research, such as 5 sit-stand tests, TUG (Trip and Go) tests, and stair climbing/descending tests. • Having a walking speed of at least 0.4 m/s or more as a result of the 4 Meter Walking Test (having limited or independent mobility within the community).
- Voluntarily agreeing to participate in the study and providing informed consent.
Exclusion Criteria:
- Having a history of advanced cognitive impairment or diagnosed dementia that would impair the ability to understand and follow test instructions.
- Those diagnosed with moderate or severe cognitive impairment (MMSE < 24 and/or MoCA < 21)
- Having a walking speed below 0.4 m/s on the 4-Meter Walk Test (individuals who are wheelchair-bound or bedridden).
- Advanced Parkinson's disease, active stroke sequelae, lower extremity fracture within the last 6 months, or a history of acute orthopedic surgery that primarily affects motor performance and balance.
- Those with severe hearing or vision loss
- Individuals experiencing significant difficulty communicating
- Participants who did not sign the voluntary consent form
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 |
|---|---|
|
Geriartric Indivıduals
Geriatric individuals aged 65 and over who meet the inclusion criteria for the study.
|
Assessments will be conducted after obtaining voluntary consent from the participants.
The physical performance tests to be applied within the scope of the research will be carried out by the research team within the framework of internationally accepted standard protocols whose validity and reliability have been proven in the geriatric population.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
4-Meter Walk Test (Walking Speed Measurement)
Time Frame: 1 week
|
Walking speed will be assessed using the 4-Meter Walk Test, a key indicator of functional mobility in geriatric individuals.
Participants will be asked to walk a 4-meter test area in the center at their "natural and comfortable walking speed," using 1-meter "acceleration" zones at the beginning and 1-meter "deceleration" zones at the end of a 6-meter flat course.
The measurement will be recorded with a stopwatch the moment the participant's foot crosses the 4-meter marked area, and the result will be calculated in m/s (Studenski et al., 2011).
|
1 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time Sit-Stand Test (5STS):
Time Frame: 1 week
|
To assess lower extremity muscle strength and balance, participants will be asked to stand up and sit down as quickly as possible, five times consecutively, from a standard chair 43-45 cm high, with their arms crossed over their chest.
The timer will start with the "start" command and end when the fifth sitting is completed (Bohannon, 2006).
|
1 week
|
|
Timed Up and Go (TUG):
Time Frame: 1 week
|
To measure functional mobility, the participant will get up from the chair, walk a distance of 3 meters, return, and sit back down in the chair.
This time will be recorded in seconds using a stopwatch (Podsiadlo & Richardson, 1991).
|
1 week
|
|
Functional Reach Test (FUT/FRT)
Time Frame: 1 week
|
To measure static balance and stability limits, the maximum distance the participant can reach without losing balance and without taking a step, while standing next to a wall with the shoulder flexed at 90 degrees, will be measured (Duncan et al., 1990).
|
1 week
|
|
Single Leg Balance Test (Right and Left):
Time Frame: 1 week
|
Participants' static balance will be determined by recording the "time they can stand on one leg" (maximum 60 seconds) with their eyes open and hands on their hips, on both their dominant and non-dominant legs (Springer et al., 2007).
|
1 week
|
|
Flexibility (Sit-and-Reach Test):
Time Frame: 1 week
|
To measure hamstring and lower back flexibility, the participant will sit in a long, straight position, reaching forward without bending their knees.
The distance reached by their fingertips will be recorded on a "sit-and-reach bench" (Wells & Dillon, 1952).
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1 week
|
|
Stair Climbing Test
Time Frame: 1 week
|
To assess high-level mobility, participants will be recorded in seconds for safely and as quickly as possible ascending and descending a staircase of standard step height [a specified number of steps, e.g., 10 steps] (Nightingale et al., 2003).
|
1 week
|
|
Strength Measurement (Hand Grip Strength):
Time Frame: 1 week
|
Upper extremity muscle strength will be measured using a digital hand dynamometer according to the ASHT (American Society of Hand Therapists) protocol.
Participants will be asked to grip with maximum force while sitting upright, with shoulder adduction and elbow 90 degrees flexed.
Three repetitions will be performed for each hand, and the average of these measurements in kilograms (kg) will be included in the analysis (Roberts et al., 2011; Cruz-Jentoft et al., 2019).
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Abellan van Kan G, Rolland Y, Andrieu S, Bauer J, Beauchet O, Bonnefoy M, Cesari M, Donini LM, Gillette Guyonnet S, Inzitari M, Nourhashemi F, Onder G, Ritz P, Salva A, Visser M, Vellas B. Gait speed at usual pace as a predictor of adverse outcomes in community-dwelling older people an International Academy on Nutrition and Aging (IANA) Task Force. J Nutr Health Aging. 2009 Dec;13(10):881-9. doi: 10.1007/s12603-009-0246-z.
- Middleton A, Fritz SL, Lusardi M. Walking speed: the functional vital sign. J Aging Phys Act. 2015 Apr;23(2):314-22. doi: 10.1123/japa.2013-0236. Epub 2014 May 2.
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 (Estimated)
May 1, 2026
Primary Completion (Estimated)
May 15, 2026
Study Completion (Estimated)
August 30, 2026
Study Registration Dates
First Submitted
April 25, 2026
First Submitted That Met QC Criteria
April 25, 2026
First Posted (Actual)
May 1, 2026
Study Record Updates
Last Update Posted (Actual)
May 1, 2026
Last Update Submitted That Met QC Criteria
April 25, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2026/46
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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