Mental FatigueNCT07263334
Does Mental Fatigue Caused by Social Media Use Affect Biomechanical Properties of Muscles in Young Male Athletes?
A study testing Metal Fatigue Protocols in people with Mental Fatigue and Socail Media Usage, run by Bandırma Onyedi Eylül University at 1 site in Turkey (Türkiye).
Trial summary
The aim of this study is to examine the effect of mental fatigue (MF) induced by 30 minutes of social media use on neck kinematics and neck muscle biomechanical properties in young male athletes. Twenty-five participants are enrolled in a single-blind cross-sectional design. Read more about this study
- Who is it for?
- Ages 18 to 35 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Mental Fatigue, Socail Media Usage, Cervical Range of Motion
- What is being tested?
- Metal Fatigue Protocols
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 25 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Jun 2024to 1 Feb 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 35 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Amateur athletes aged 18-35
- using social media via a smartphone
- actively participating in competitions
Who cannot join
- having a surgical operation or trauma related to the neck region, having any pathology in the neck region (neck cyst, tumours, haematoma, etc.), having a history of traumatic injury in the neck region, and having neurological and rheumatic diseases.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effect of Text Neck Syndrome on the Muscle and Bone Architecture of the Cervical Region
The aim of this study is to examine the effect of mental fatigue (MF) induced by 30 minutes of social media use on neck kinematics and neck muscle biomechanical properties in young male athletes. Twenty-five participants are enrolled in a single-blind cross-sectional design. Baseline and post-MF assessments include cervical range of motion measured with a CROM device, forward head posture evaluated using craniovertebral angle analysis, and muscle tone, stiffness, and elasticity measured with MyotonPRO. MF is induced through 30 minutes of Instagram® use on a smartphone and quantified with a 100-mm Visual Analogue Scale (VAS). No results or conclusions are provided in this section.
Read the detailed description
The aim of this study is to investigate the effect of mental fatigue (MF) induced by 30 minutes of social media use on neck kinematics and the biomechanical properties of the neck muscles [upper trapezius, sternocleidomastoid (SCM), semispinalis (SS), and splenius capitis (SC)] in young male athletes. Twenty-five young male athletes are enrolled in a single-blind cross-sectional study. Participants undergo assessments at baseline and again following MF induction. These assessments include cervical range of motion (CROM) measured with a validated CROM device, forward head posture (FHP) evaluated via craniovertebral angle (CVA) photometric analysis, and muscle biomechanical properties (tone, stiffness, elasticity) measured using the MyotonPRO device. Mental fatigue is induced through 30 minutes of Instagram use on a smartphone. MF severity is assessed using a 100-mm Visual Analogue Scale (VAS). No results or conclusions are reported in this section.
- Conditions
- Mental Fatigue, Socail Media Usage, Cervical Range of Motion
- Being tested
- Metal Fatigue Protocols
- Medical subject headings
- Mental Fatigue
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Metal Fatigue ProtocolsOther
Metal Fatigue Protocols Participants used Instagram® for 30 minutes by browsing their personal feed with one-handed tapping and swiping gestures. They were allowed to scroll and like posts but were restricted from viewing stories or reels and from sharing any content.
| Study group | Role | What they receive |
|---|---|---|
| Experimental Design | Experimental | The study was conducted as a single-blind experimental study. Since it was thought that mental functions might be affected, all the procedures to be applied were explained to the participants, and written informed consent was obtained, but the purpose and hypotheses were not explained. After the final assessment of the participants was completed, the purpose and hypotheses of this study were explained. The study was conducted between June 2024 and February 2025. Receives: Other: Metal Fatigue Protocols |
What is being measured
The primary outcome is the main question the study is designed to answer.
Range of Motion of the Neck
The normal joint motion of the cervical region was evaluated with the Cervical Range of Motion (CROM-Perfomance Attainment Associates, St. Paul, MN, 55117, United States) device, which has clinical validity and reliability. The flexion, extension, right and left lateral flexion and rotation angles of the cervical region were measured three times and averaged with the CROM device.
Measured: Baseline
Forward Head Posture
The craniovertebral angle (CVA) was measured using a photometric method with the participants in a standing position. Prior to imaging, the C7 process and tragus were marked. A camera was placed 1.5 m from the lateral surface of the body at the level of the acromial process.
Measured: Baseline
Biomechanical Properties of Muscles
The biomechanical properties of cervical muscles were assessed using the MyotonPRO, which quantifies tissue oscillations following a brief mechanical impulse to determine tone, stiffness, and elasticity. This method provides reliable interrater and intrarater measurements for cervical musculature when applied perpendicularly in a standardized supine position, as demonstrated in previous research. For each muscle, three consecutive measurements were recorded following established protocols for the sternocleidomastoid and upper trapezius.The MyotonPro enables the assessment of various parameters, including the state of resting muscle tone (F), defined as the suppressed EMG signal, and dynamic stiffness (S). The basis of stiffness assessment using myotonometry is the theory of free oscillations, arising from the natural oscillations of tissues in response to brief mechanical exposure of the skin.
Measured: Baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Dec 2025
- Study start1 Jun 2024
- Primary completion20 Dec 2024
- Study completion1 Feb 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Mental FatigueStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Some of the researchers (O.B.T., B.A., M.B.U.) performed all assessments. To avoid any bias, group information was kept confidential,and statistical analyses were performed by another researcher (A.K., B.Ç., A.G.).
- Masking
- None (open label)
- Enrolment
- 25 participants (actual)
Sponsor and investigators
- Lead sponsor
- Bandırma Onyedi Eylül University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Burçin Akçay, Dokuz Eylul University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07263334
- Sponsor's protocol ID
- 2024-110
- Status last verified
- Nov 2025
- First submitted
- 22 Mar 2025
- Last updated
- 4 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Text Neck Syndrome on the Muscle and Bone Architecture of the Cervical Region
- ClinicalTrials.gov ID
- NCT07263334
- Acronym / sponsor ID
- 2024-110
- Conditions
- Mental Fatigue, Socail Media Usage, Cervical Range of Motion
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 25 participants (actual)
- Lead sponsor
- Bandırma Onyedi Eylül UniversityUniversity, hospital or other
- Study start
- 1 Jun 2024 (actual)
- Primary completion
- 20 Dec 2024 (actual)
- Study completion
- 1 Feb 2025 (actual)
- First posted
- 4 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to examine the effect of mental fatigue (MF) induced by 30 minutes of social media use on neck kinematics and neck muscle biomechanical properties in young male athletes. Twenty-five participants are enrolled in a single-blind cross-sectional design. Baseline and post-MF assessments include cervical range of motion measured with a CROM device, forward head posture evaluated using craniovertebral angle analysis, and muscle tone, stiffness, and elasticity measured with MyotonPRO. MF is induced through 30 minutes of Instagram® use on a smartphone and quantified with a 100-mm Visual Analogue Scale (VAS). No results or conclusions are provided in this section.
Detailed description
The aim of this study is to investigate the effect of mental fatigue (MF) induced by 30 minutes of social media use on neck kinematics and the biomechanical properties of the neck muscles [upper trapezius, sternocleidomastoid (SCM), semispinalis (SS), and splenius capitis (SC)] in young male athletes. Twenty-five young male athletes are enrolled in a single-blind cross-sectional study. Participants undergo assessments at baseline and again following MF induction. These assessments include cervical range of motion (CROM) measured with a validated CROM device, forward head posture (FHP) evaluated via craniovertebral angle (CVA) photometric analysis, and muscle biomechanical properties (tone, stiffness, elasticity) measured using the MyotonPRO device. Mental fatigue is induced through 30 minutes of Instagram use on a smartphone. MF severity is assessed using a 100-mm Visual Analogue Scale (VAS). No results or conclusions are reported in this section.
Study design
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Some of the researchers (O.B.T., B.A., M.B.U.) performed all assessments. To avoid any bias, group information was kept confidential,and statistical analyses were performed by another researcher (A.K., B.Ç., A.G.).
| Arm | Type | Receives |
|---|---|---|
| Experimental Design | Experimental | Other: Metal Fatigue ProtocolsThe study was conducted as a single-blind experimental study. Since it was thought that mental functions might be affected, all the procedures to be applied were explained to the participants, and written informed consent was obtained, but the purpose and hypotheses were not explained. After the final assessment of the participants was completed, the purpose and hypotheses of this study were explained. The study was conducted between June 2024 and February 2025. |
Who may qualify
- Ages
- 18 to 35 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Amateur athletes aged 18-35
- using social media via a smartphone
- actively participating in competitions
Key exclusion criteria (1 listed)
- having a surgical operation or trauma related to the neck region, having any pathology in the neck region (neck cyst, tumours, haematoma, etc.), having a history of traumatic injury in the neck region, and having neurological and rheumatic diseases.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Metal Fatigue ProtocolsMetal Fatigue Protocols Participants used Instagram® for 30 minutes by browsing their personal feed with one-handed tapping and swiping gestures. They were allowed to scroll and like posts but were restricted from viewing stories or reels and from sharing any content. | Other | Experimental Design |
Primary outcome
Range of Motion of the Neck
Time frame: Baseline
The normal joint motion of the cervical region was evaluated with the Cervical Range of Motion (CROM-Perfomance Attainment Associates, St. Paul, MN, 55117, United States) device, which has clinical validity and reliability. The flexion, extension, right and left lateral flexion and rotation angles of the cervical region were measured three times and averaged with the CROM device.
Forward Head Posture
Time frame: Baseline
The craniovertebral angle (CVA) was measured using a photometric method with the participants in a standing position. Prior to imaging, the C7 process and tragus were marked. A camera was placed 1.5 m from the lateral surface of the body at the level of the acromial process.
Biomechanical Properties of Muscles
Time frame: Baseline
The biomechanical properties of cervical muscles were assessed using the MyotonPRO, which quantifies tissue oscillations following a brief mechanical impulse to determine tone, stiffness, and elasticity. This method provides reliable interrater and intrarater measurements for cervical musculature when applied perpendicularly in a standardized supine position, as demonstrated in previous research. For each muscle, three consecutive measurements were recorded following established protocols for the sternocleidomastoid and upper trapezius.The MyotonPro enables the assessment of various parameters, including the state of resting muscle tone (F), defined as the suppressed EMG signal, and dynamic stiffness (S). The basis of stiffness assessment using myotonometry is the theory of free oscillations, arising from the natural oscillations of tissues in response to brief mechanical exposure of the skin.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Dec 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Metal Fatigue Protocols in people with Mental Fatigue and Socail Media Usage, run by Bandırma Onyedi Eylül University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Range of Motion of the Neck (time frame: Baseline). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Dec 2025.