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Enrolling by invitationNCT06826209Updated Feb 13, 2025

Comparison of Upper Extremity Functional Performance in Hemophilic and Healthy Children

An observational study in Hemophilia, Upper Extremity and Strength, sponsored by Hacettepe University. Enrolling by invitation at 1 site in Turkey (Türkiye). Open to male participants aged 7 Years to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-02-13.

Sponsored by Hacettepe University · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2026, 4 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
30
Ages
7 Years to 17 Years
Sex
Male
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Study summary

The goal of this observational study is to evaluate the functional performance of the upper extremity joints (scapula, shoulder, elbow, and wrist) in haemophilic children and compare muscle strength and ADL limitations with healthy children.

Read the detailed description

This study aims to evaluate the upper extremity functional performance, muscle strength, and daily living activity levels of hemophilic children and compare them with healthy children. The goal is to determine the effects of hemophilia on these children and contribute to the development of appropriate rehabilitation strategies. Parameters include explosive strength, isometric muscle strength, wrist grip strength, and functional exercise capacity. Additionally, the ADL-Glittre pediatric version test and Hemophilia Joint Health Score (HJHS) will be used to assess joint health and GYA performance. Muscle strength is crucial for hemophilic children to perform daily activities, and the relationship between muscle strength and GYA levels will be investigated. The project aims to guide the development of physiotherapy and rehabilitation strategies for hemophilic children and contribute to the literature by filling existing gaps, ultimately creating an important reference for healthcare professionals and families.

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Conditions studied

  • Hemophilia
  • Upper Extremity
  • Strength
  • Performance
  • Children

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Keywords

  • Hemophilia
  • Muscle Strength
  • Upper Extremity
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In context

Hemophilia A

885 studies on the registry are indexed under Hemophilia A; 139 are open to participants now.

This study's planned enrollment of 30 is below the median of 80 across 322 observational studies indexed under Hemophilia A.

Browse Hemophilia A studies →

Lead sponsor

Hacettepe University is the lead sponsor of 1,001 studies on the registry; 215 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
7 Years to 17 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Male children diagnosed with Hemophilia, who are being followed by the same physician at the Hematology Unit of the Department of Pediatrics, Faculty of Medicine, Hacettepe University, will be included in the study

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Diagnosed with Hemophilia A or B
  • Receiving prophylaxis treatment (a routine treatment)
  • Negative for inhibitors at the time of enrollment

Exclusion criteria

Exclusion Criteria:

  • Positive for inhibitors at the time of enrollment
  • Acute elbow bleeding
  • History of acute muscle bleeding
  • History of surgery in any upper extremity joints
  • Having undergone radionuclide synovectomy
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • Hemophilia groups

    Patients group

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What researchers measure

Primary outcomes

  1. Hemophilia Joint Health Score

    The Hemophilia Joint Health Score (HJHS) is a clinical tool used to assess joint health in individuals with hemophilia, focusing on major joints such as the knees, elbows, and ankles. It evaluates symptoms like pain, swelling, and range of motion restrictions, with a grading system that helps determine the severity of joint damage. The HJHS also considers joint function in daily activities, making it an essential tool for monitoring joint health and the progression of hemophilic arthropathy. It plays a vital role in both clinical management and research, helping guide treatment strategies and assess their effectiveness.

    Time frame: Through study completion, an average of 1 year

Secondary outcomes

  1. Muscle Strength

    The Lafayette Handheld Dynamometer is a device used to measure upper extremity muscle strength in children with hemophilia. It assesses muscle strength under isometric conditions and is typically used to test the muscles around the shoulder, elbow, and wrist. The measurements aim to determine the maximum force exerted by the muscles, which is important for identifying potential reductions in muscle strength in individuals with hemophilia. This test is valuable for determining physical performance levels, planning treatment approaches, and guiding rehabilitation processes.

    Time frame: Through study completion, an average of 1 year

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Study locations

1 site
  • Hacettepe Universit
    Ankara, Ankara 06100, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: Undecided — Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 13, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06826209
Responsible party
Ferhat Öztürk (Researcher, Hacettepe University) — Principal investigator
First posted
Feb 13, 2025
Start date
Oct 24, 2024
Primary completion
Jun 24, 2026 (estimated)
Completion
Oct 24, 2026 (estimated)
Last update
Feb 13, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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