- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05938153
Evaluation of Metabolic Syndrome, Frailty, Locomotive Syndrome, Balance and Physical Fitness in Elderly Individuals
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Kırıkkale
-
Kırıkkale, Kırıkkale, Turkey (Türkiye), 71450
- Kırıkkale University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals aged 65 and over,
- Volunteering to participate in the research
- No cooperation and communication problems
Exclusion Criteria:
- Individuals with neurological and orthopedic problems
- Uncontrolled hypertension
- Those with cardiac disorders
- Those with cooperation and communication problems
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
geriatrics individuals
|
Geriatric Locomotive Function Scale: This scale consists of a questionnaire of 25 items that can be easily understood by the elderly and each item is graded between 0 and 4 points. The total score is the result of the sum of all items ranging from 0 to 100; the higher the score, the higher the physical impairment of the elderly, with a score of 16 being the cut-off point for locomotive syndrome. The GLFS-25 includes 4 questions about pain, 16 questions about activities of daily living, 3 questions about social performance and 2 questions about mental health status to assess geriatric individuals. Turkish validity and reliability of the questionnaire was conducted by Sadikoglu. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Geriatric Locomotive Function Scale:
Time Frame: 10 minute
|
This scale consists of a questionnaire of 25 items that can be easily understood by the elderly and each item is graded between 0 and 4 points.
The total score is the result of the sum of all items ranging from 0 to 100; the higher the score, the higher the physical impairment of the elderly, with a score of 16 being the cut-off point for locomotive syndrome.
The GLFS-25 includes 4 questions about pain, 16 questions about activities of daily living, 3 questions about social performance and 2 questions about mental health status to assess geriatric individuals.
Turkish validity and reliability of the questionnaire was conducted by Sadikoglu.
|
10 minute
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Chair sit-lie test
Time Frame: 5 minute
|
The patient is asked to sit and stand as quickly as possible in a chair with a seat height of 43.2 cm and a supported back.
The patient sits on the chair.He crosses his hands on his chest. 2 attempts are made before the test.
A stopwatch is kept for 30 seconds and the number of sit-ups is noted.
Less than 10 sit-ups in 30 seconds indicates lower extremity muscle weakness
|
5 minute
|
|
Two-minute step test
Time Frame: 2 minute
|
It is applied to evaluate aerobic endurance.
In order to perform the test correctly, the distance at which the participant will lift the knee is determined as the midpoint between the knee joint and the crista iliaca and marked on the wall.
For a better understanding of the test is demonstrated practically.
The participant is asked to start with the right foot and rhythmically raise their feet to the marked height for 2 minutes.
The number of standardized right steps repeated for two minutes is recorded as a score.
|
2 minute
|
|
Weight lifting test
Time Frame: 2 minute
|
It is applied to evaluate upper extremity muscle strength.
Participant's feet is asked to sit towards the side of the chair while on the floor.
The participant is asked to bend and extend their arms by lifting the dumbbell with the given instruction.
As weight dumbbells of 3.63 kg for men (8-lb) and 2.27 kg for women (5-lb) are used.
For a better understanding of the test, it was demonstrated and practiced.
In the test, the maximum possible number of repetitions performed with the dominant arm for 30 s is considered as the score.
|
2 minute
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Gurbuz02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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