- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06288789
Turkish Validity and Reliability of the Social Frailty Index
April 24, 2024 updated by: Elif Gur Kabul, Pamukkale University
Turkish Validity and Reliability of the Social Frailty Index in the Older Adults
The aim was to examine the validity and reliability of the Social Frailty Index in Turkish among older adults.
65 years and above older adults will be included included in the study.
Older adults who agree to participate in the study will first be administered the Hodkinson Mental Test.
Those who score 6 points and above will be included in the study.
To evaluate the validity of the "Social Frailty Index", Social Inclusion Scale, Older people's quality of life-brief (OPQOL-brief) and Lubben Social Network Scale will be applied to the participants.
To determine the reliability of the "Social Frailty Index", older adults who do not receive any treatment will be tested and re-tested at one-week intervals.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
186
Phase
- Not Applicable
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
-
-
Merkez
-
Usak, Merkez, Turkey, 64200
- Elif Gur Kabul
-
-
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
Description
Inclusion Criteria:
- Getting a score of 6 or above on the Hodkinson Mental Test
Exclusion Criteria:
- -Having another chronic disease that can cause pain
- Having a neurological disease
- Being blind
- Having an orthopedic, neurological or mental disability
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
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
65 years and above older adults
|
Social Frailty Index will be applied twice, one week apart.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Frailty Index
Time Frame: 10 minutes
|
Social Frailty Index included age, gender and eight social predictors
|
10 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Socıal Inclusıon Scale
Time Frame: 10 minutes
|
It consists of 22 items
|
10 minutes
|
|
Older people's quality of life-brief (OPQOL-brief)
Time Frame: 8 minutes
|
It consists of 13 items
|
8 minutes
|
|
Lubben Social Network Scale
Time Frame: 5 minutes
|
It consists of 6 items
|
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)
February 25, 2024
Primary Completion (Actual)
March 20, 2024
Study Completion (Actual)
March 30, 2024
Study Registration Dates
First Submitted
February 24, 2024
First Submitted That Met QC Criteria
February 24, 2024
First Posted (Actual)
March 1, 2024
Study Record Updates
Last Update Posted (Actual)
April 25, 2024
Last Update Submitted That Met QC Criteria
April 24, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SFI-TR
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
product manufactured in and exported from the U.S.
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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