- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06561113
The Effect of Turkish Coffee on Postural Control and Hand-eye Coordination in Young Adults
August 23, 2024 updated by: Deniz Tuncer, Bezmialem Vakif University
Does a Cup of Turkish Coffee Affect Postural Control and Hand-eye Coordination in Young Adults? A Quasi-experimental Study
Although the effects of different doses of caffeine on balance have been evaluated in various studies, the effects of low doses of caffeine ingested with Turkish coffee on postural control and hand-eye coordination remain unclear.
In this study, it will be investigated the acute effects of 60 mg caffeine intake via Turkish coffee on postural control and hand-eye coordination.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This study is designed as a one-group pretest-posttest quasi-experimental research.
The study will be conducted with healthy young adults with low coffee consumption habits.
Participants who meet the inclusion and exclusion criteria will undergo postural control assessment with the Biodex Balance System® and hand-eye coordination test with the Alternate Hand Wall Toss Test.
Subjects will be given 65 ml of Turkish coffee (one cup) to ensure oral caffeine intake.
The same assessments will be repeated 30 minutes after caffeine intake.
Study Type
Interventional
Enrollment (Actual)
20
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
-
-
-
Istanbul, Turkey
- Bezmialem Vakif 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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being 18-26 years of age
- Having a normal body mass index
Exclusion Criteria:
- Having a health problem that prevented caffeine intake
- Having a diagnosis of vestibular and neurological disease
- Using drugs that affect the central nervous system
- Using any medication related to chronic disease
- Having lower extremity rotational alignment disorder
- Having a history of lower and/or upper extremity injury or surgery in the last year
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: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study group
Participants who meet the inclusion and exclusion criteria will undergo postural control assessment with the Biodex Balance System® and hand-eye coordination test with the Alternate Hand Wall Toss Test.
Subjects will be given 65 ml of Turkish coffee (one cup) to ensure oral caffeine intake.
The same assessments will be repeated 30 minutes after caffeine intake.
|
One cup of Turkish coffee contains 60 mg/65 ml (1 Turkish coffee cup) of caffeine.
Participants will be instructed to sit for 10 minutes before drinking coffee.
To prepare the Turkish coffee, 5 g of ground dry coffee will be mixed in 100 mL of tap water and left to boil in a coffee machine.
When the first boil starts, it will be removed from the machine and poured into the cup.
Then, 65 ml of Turkish coffee will be given to the subjects to ensure oral caffeine intake.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postural control assessment with Biodex Balance System
Time Frame: Baseline and immediately after caffeine intake
|
Postural control evaluation will be performed with "Biodex Balance System" (Shirley, NY).
Three tests will be performed with the device: postural stability test, stability limits test, and the Modified Clinical Test for Sensory Interaction and Balance (mCTSIB).
The test will then continue for 30 seconds, during which time the number of balls caught will be noted
|
Baseline and immediately after caffeine intake
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hand-eye coordination assessment with alternate hand-wall toss test
Time Frame: Baseline and immediately after caffeine intake
|
Alternate hand wall toss test will be used to measure hand-eye coordination.
The Alternate-Hand Wall-Toss Test is a test of hand-eye coordination, where the participant throw a ball against a wall from one hand in an underarm action, and attempt to catch it with the opposite hand.
The test will then continue for 30 seconds, during which time the number of balls caught will be noted.
|
Baseline and immediately after caffeine intake
|
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)
August 14, 2024
Primary Completion (Actual)
August 23, 2024
Study Completion (Actual)
August 23, 2024
Study Registration Dates
First Submitted
August 13, 2024
First Submitted That Met QC Criteria
August 17, 2024
First Posted (Actual)
August 19, 2024
Study Record Updates
Last Update Posted (Actual)
August 26, 2024
Last Update Submitted That Met QC Criteria
August 23, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 29.07.2024-159880
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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