NCT07126899

Brief 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. Identifying the characteristics of these injuries, many of which occur through preventable mechanisms, is crucial for guiding preventive measures.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
64

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 13, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

August 11, 2025

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 15, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 17, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2025

Completed
Last Updated

August 17, 2025

Status Verified

August 1, 2025

Enrollment Period

5 months

First QC Date

August 11, 2025

Last Update Submit

August 11, 2025

Conditions

ADHD - Attention Deficit Disorder With HyperactivityTendon Injuries

Outcome Measures

Primary Outcomes (1)

  • ASRS-Barratt-Anger

    3 months

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
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.

You may qualify if:

  • Those with tendon injuries,
  • Those aged between 18 and 65,
  • Those with good cognitive function,

You may not qualify if:

  • Tendon injury diagnosis is uncertain,
  • Cognitive function is poor,

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Yozgat Bozok University

Yozgat, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Attention Deficit Disorder with HyperactivityTendon Injuries

Condition Hierarchy (Ancestors)

Attention Deficit and Disruptive Behavior DisordersNeurodevelopmental DisordersMental DisordersWounds and Injuries

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 11, 2025

First Posted

August 17, 2025

Study Start

March 13, 2025

Primary Completion

August 15, 2025

Study Completion

September 1, 2025

Last Updated

August 17, 2025

Record last verified: 2025-08

Locations

TU(1)