ADHD - Attention Deficit Disorder With HyperactivityTendon-ADHDNCT07126899
Hand Tendon Injuries: An Investigation Of Attention Deficit Disorder
An observational study of ADHD - Attention Deficit Disorder With Hyperactivity and Tendon Injuries, run by Atılım University at 1 site in Turkey (Türkiye).
Trial summary
Tendon injuries cause significant disability, loss of work capacity, and economic burden. The injury itself and its consequences impact individuals not only in terms of their ability to work but also socially and psychologically. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- ADHD - Attention Deficit Disorder With Hyperactivity, Tendon Injuries
- How many people
- 64 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 13 Mar 2025to 1 Sep 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: The medical history and results of completed scales for patients aged between 18 and 65 with good cognitive function will be recorded on the patient form. The medical history and results of completed scales for healthy individuals aged between 18 and 65 with good cognitive function, who are of similar age and gender to the patient group, have no tendon injuries, and will be recorded on the control form.
Who may be able to join
- Those with tendon injuries,
- Those aged between 18 and 65,
- Those with good cognitive function,
Who cannot join
- Tendon injury diagnosis is uncertain,
- Cognitive function is poor,
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Hand Tendon Injuries: Investigation of Attention Deficit, Hyperactivity, Impulsivity, Anger, and Anxiety Levels - Case-Control Study
Tendon injuries cause significant disability, loss of work capacity, and economic burden. The injury itself and its consequences impact individuals not only in terms of their ability to work but also socially and psychologically. Identifying the characteristics of these injuries, many of which occur through preventable mechanisms, is crucial for guiding preventive measures.
- Medical subject headings
- Attention Deficit Disorder with Hyperactivity, Tendon Injuries
What is being measured
The primary outcome is the main question the study is designed to answer.
ASRS-Barratt-Anger
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Aug 2025
- Study start13 Mar 2025
- Primary completion15 Aug 2025 (estimated)
- Study completion1 Sep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for ADHD - Attention Deficit Disorder With HyperactivityStudies 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
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 64 participants (actual)
Sponsor and investigators
- Lead sponsor
- Atılım University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07126899
- Sponsor's protocol ID
- 2024-GOKAEK-2411_2024.10.16_16
- Acronym
- Tendon-ADHD
- Status last verified
- Aug 2025
- First submitted
- 11 Aug 2025
- Last updated
- 17 Aug 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Agtas Ertan E, Demir Karakilic G, Ertan MB. Impulsivity and inattention in hand tendon injuries: a case-control study revealing distinct profiles for work-related accidents. Arch Orthop Trauma Surg. 2026 May 27;146(1):203. doi: 10.1007/s00402-026-06354-9.
PubMed 42203947
Study at a glance
From the registry record, last updated by the sponsor on 17 Aug 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Hand Tendon Injuries: Investigation of Attention Deficit, Hyperactivity, Impulsivity, Anger, and Anxiety Levels - Case-Control Study
- ClinicalTrials.gov ID
- NCT07126899
- Acronym / sponsor ID
- Tendon-ADHD / 2024-GOKAEK-2411_2024.10.16_16
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 64 participants (actual)
- Lead sponsor
- Atılım UniversityUniversity, hospital or other
- Study start
- 13 Mar 2025 (actual)
- Primary completion
- 15 Aug 2025 (estimated)
- Study completion
- 1 Sep 2025 (estimated)
- First posted
- 17 Aug 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.
Tendon injuries cause significant disability, loss of work capacity, and economic burden. The injury itself and its consequences impact individuals not only in terms of their ability to work but also socially and psychologically. Identifying the characteristics of these injuries, many of which occur through preventable mechanisms, is crucial for guiding preventive measures.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- The medical history and results of completed scales for patients aged between 18 and 65 with good cognitive function will be recorded on the patient form. The medical history and results of completed scales for healthy individuals aged between 18 and 65 with good cognitive function, who are of similar age and gender to the patient group, have no tendon injuries, and will be recorded on the control form.
Key inclusion criteria (3 listed)
- Those with tendon injuries,
- Those aged between 18 and 65,
- Those with good cognitive function,
Key exclusion criteria (2 listed)
- Tendon injury diagnosis is uncertain,
- Cognitive function is poor,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
ASRS-Barratt-Anger
Time frame: 3 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Aug 2025.
- Derived from this study: PubMed 42203947Agtas Ertan E, Demir Karakilic G, Ertan MB. Impulsivity and inattention in hand tendon injuries: a case-control study revealing distinct profiles for work-related accidents. Arch Orthop Trauma Surg. 2026 May 27;146(1):203. doi: 10.1007/s00402-026-06354-9.
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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?
An observational study of ADHD - Attention Deficit Disorder With Hyperactivity and Tendon Injuries, run by Atılım 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 2 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: under way, not looking for participants, as of the sponsor's last update on 17 Aug 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?
This study is still under way. Results are not available in the source record yet.
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?
ASRS-Barratt-Anger (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07126899, which also lists 1 linked publication.
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 17 Aug 2025.