Postural Stability and Ankle Mobility in Haglund Syndrome
NCT ID: NCT05905952
Last Updated: 2023-06-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
25 participants
OBSERVATIONAL
2023-03-12
2023-09-01
Brief Summary
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Detailed Description
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* Total sample size is fifty participants, twenty five patient of symptomatic Haglund syndrome of both gender and twenty five healthy volunteers of matched age, sex and body mass index without any musculoskeletal complaints of the lower limbs.
* Biodex balance system will be used to determine postural stability.
* Ankle plantarflexion and dorsiflexion range of motion will be measured using an Electrogoniometer.
* Age of the patients 25-56
* BMI of (18.5 to 24.9)
Participants:
Fifty volunteers from both genders will participate in the study. They will be assigned from outpatient clinic of Faculty of Physical Therapy, Deraya University. They will be interviewed and divided to twenty five patient of Haglund syndrome as (patient group) after being diagnosed and referred by orthopedic surgeon and twenty five Healthy volunteers as (control group) based on the following inclusion and exclusion criteria:
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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patient group
to twenty five patient of Haglund syndrome as (patient group) after being diagnosed and referred by orthopedic surgeon and twenty
balance and ROM assessment
assessment of postural stability and ankle range of motion
control group
twenty five Healthy volunteers as (control group) based on the following inclusion and exclusion criteria
balance and ROM assessment
assessment of postural stability and ankle range of motion
Interventions
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balance and ROM assessment
assessment of postural stability and ankle range of motion
Eligibility Criteria
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Inclusion Criteria
* Patient referred from orthopedic surgeon with diagnoses as Haglund syndrome according to the following signs and symptoms
* Calcaneal prominence diagnosed on lateral weight bearing radiograph with bony prominence superior to parallel pitch lines or posterior calcaneal angle greater than 75 degrees
* Pain medially at insertion of tendo-achilles
* Palpation of hard, bony prominence
* Pain upon rising out of bed
* Both unilateral and bilateral cases, and in consideration of dealing with bilateral cases the tested limb will be the most painful limb.
* Age of 25-56 years
* Both males and females.
* BMI of (18.5 to 24.9)
For control group:
Healthy volunteers of matched age, sex and body mass index without any musculoskeletal complaints of the lower limbs and will be included in the control group in this study .
Exclusion Criteria
* cognitive disorder, visual impairment that affected their daily living and any further medical condition that would prohibit them from participating safely in the chosen balance measures
* sensory loss at foot or ankle and with a systemic inflammatory disease, such as diabetes mellitus, peripheral neuropathy, rheumatoid arthritis and ankylosing spondylitis, who had undergone corticosteroid injections or physical therapy in the last three months
* Patients with vestibular or neurological disorders
* Any other cause of posterior heel pain.
25 Years
56 Years
ALL
Yes
Sponsors
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Cairo University
OTHER
Responsible Party
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Nassif Magdy Mousa
principle investigator
Principal Investigators
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enas F youssif, prof
Role: PRINCIPAL_INVESTIGATOR
Cairo University
Locations
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Deraya University
Minya, , Egypt
Countries
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Central Contacts
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enas F youssif, prof
Role: CONTACT
Facility Contacts
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mohamed A abdelmegeed, PHD
Role: backup
Other Identifiers
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P.T.REC/ 012/004497
Identifier Type: -
Identifier Source: org_study_id
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