- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05173129
Posture Analysis for Patients With Haemophilia
August 3, 2022 updated by: Volkan Deniz, PT, Cukurova University
Comparison of Posture and Muscle Stiffness of Adolescent Boys With Haemophilia and Those of Age-matched Healthy Peers: a Controlled Cross-sectional Study
Hemophilia A and B are inherited disorders characterized by deficient or missing coagulation factors VIII or IX, respectively, of which the main long-term clinical manifestation is joint damage.
Patients with haemophilia (PwH) are susceptible to clinical joint bleeding that may cause irreversible joint damage.
Some degree of damage may already occur after the first haemarthrosis or even in children who never experienced clinically evident joint bleeds.
Joints are mechanical systems with a structure strictly related to functioning.
Therefore, any alteration in structure may have an impact on function (starting from the primary level of posture and anti-gravity muscles), which might in turn stress the joints and increase the risk of bleeding.The primary aim of this study is to investigate the changes in posture and the mechanical properties of anti-gravity muscles of adolescent PwH.
The secondary aim is to determine the effect of joint dysfunction on posture in adolescent PwH.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
44
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
-
-
-
Adana, Turkey, 01100
- Çukurova 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
10 years to 19 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Adolescent boys with haemophilia A or haemophilia B (for experimental group) and healthy adolescent boys (for control group).
Exclusion Criteria:
- To be with another congenital coagulopathy such as von Willebrand syndrome.
- To be unable to stand without support due to hemophilic arthropathy.
- To be having another musculoskeletal problem.
- To be having factor VIII or IX level in the plasma above 6%
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Haemophilic boys
Adolescent boys with haemophilia
|
Posture analysis and assessment of mechanical properties of posture muscles
|
|
Active Comparator: Healthy boys
Healthy adolescent boys
|
Posture analysis and assessment of mechanical properties of posture muscles
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Photogrammetry
Time Frame: Baseline
|
The photogrammetry is a single evaluation method based on the analysis of two-dimensional photographs with a software.The erect-static posture of the participants will be analyzed with photogrammetry method.
Firstly, two-dimensional photographs of the participant in the static-erect position will be taken.Afterwards, spinal and extremity angles will be measured in degrees using Kinovea™ software in the two-dimensional photographs transferred to the computer.
|
Baseline
|
|
Myotonometric assessment
Time Frame: Baseline
|
Myotonometric assessment is a reliable method in which the stiffness, elasticity and tone of the muscles are evaluated with a single measurement method.The mechanical properties (tone, stiffness, and elasticity) of the superficial muscles that affect posture will be evaluated with Myoton Pro™ device (Myoton AS, Tallinn, Estonia).
With a single measurement made with Myoton Pro™ device, numerical values reflecting the mechanical properties of the muscle are obtained on the screen of the device.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Haemophilia Joint Health Score
Time Frame: Baseline
|
Joint health of adolescent patients with haemophilia will be assessed by Haemophilia Joint Health Score (HJHS).
The HJHS, is calculated by adding the global gait score to the sum of 6 joint totals.
The test could yield a minimum score of 0, which indicates healthy joint status, and a maximum score of 124 points (20 points per joint × 6+ 4 points for gait score), which indicates severe arthropathy in multiple joints
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Nevin A Guzel, Prof. Dr., Gazi University
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)
September 1, 2021
Primary Completion (Actual)
January 15, 2022
Study Completion (Actual)
February 15, 2022
Study Registration Dates
First Submitted
November 20, 2021
First Submitted That Met QC Criteria
December 10, 2021
First Posted (Actual)
December 29, 2021
Study Record Updates
Last Update Posted (Actual)
August 5, 2022
Last Update Submitted That Met QC Criteria
August 3, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 109/61
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.
Clinical Trials on Hemophilia
-
Nantes University HospitalCompletedArthropathy | Moderate HemophiliaFrance
-
ApcinteX LtdCentessa Pharmaceuticals plcTerminatedHemophilia B | Hemophilia a | Hemophilia a with Inhibitor | Hemophilia B with InhibitorGeorgia, Moldova, Republic of
-
Catalyst BiosciencesCompletedHemophilia A | Hemophilia B | Hemophilia A With Inhibitor | Hemophilia B With Inhibitor | Hemophilia A Without Inhibitor | Hemophilia B Without InhibitorBulgaria, Russian Federation
-
BayerCompletedHemophilia A; Hemophilia BIsrael
-
GWT-TUD GmbHHannover Medical School; Hoffmann-La RocheCompleted
-
Laboratoire français de Fractionnement et de BiotechnologiesLFB USA, Inc.CompletedA Phase III Study on the Safety, Pharmacokinetics and Efficacy of Coagulation Factor VIIa (PERSEPT2)Hemophilia A With Inhibitors | Hemophilia B With InhibitorsBulgaria, Ukraine, Czechia, United States, Georgia, South Africa
-
PfizerCompletedFactor VIII Deficiency, Congenital | Hemophilia A, Congenital | Factor 8 Deficiency, Congenital | Autosomal Hemophilia A | Classic Hemophilia
-
Catalyst BiosciencesCompletedHemophilia A With Inhibitor | Hemophilia B With InhibitorArmenia, Georgia, South Africa, Poland, Russian Federation
-
CSL BehringTerminatedHemophilia A With Inhibitors | Hemophilia B With InhibitorsGeorgia, Italy, Malaysia, Russian Federation, South Africa, Spain, Thailand, Ukraine, United Kingdom
-
University College, LondonRecruiting
Clinical Trials on Posture Analysis
-
Lokman Hekim ÜniversitesiCompletedTransfemoral AmputeesTurkey
-
Ozden GokcekCompletedPhysical Activity Level | Use of a Walker in Infancy | Musculoskeletal ProblemsTurkey
-
Poitiers University HospitalUnknown
-
Istanbul Arel Universitysanem sener Assoc. Prof. PhD.Enrolling by invitationQuality of Life | Motivation | Body ImageTurkey
-
Baskent UniversityCompleted
-
Baskent UniversityCompletedCerebral Palsy | Posture Disorders in ChildrenTurkey
-
Centro Universitário Augusto MottaCompletedBronchial AsthmaUnited Arab Emirates
-
Hospital Moinhos de VentoHospital Ernesto DornellesTerminated
-
Arizona State UniversityCompletedHypertension | Diabetes | Sleep
-
Amasya UniversityNot yet recruiting