Physical Capacity of Spina Bifida and Factors Affecting
NCT ID: NCT06541366
Last Updated: 2024-08-07
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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COMPLETED
2 participants
OBSERVATIONAL
2019-02-01
2020-01-01
Brief Summary
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Methods: 48 cases with spina bifida and 48 control groups in other disease groups evaluated. A physiotherapist physically evaluated the cases after their personal information was obtained. A survey form examining the possible factors in the etiology of spina bifida was applied to the families.
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Detailed Description
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The case group consisted of patients who were diagnosed in the Neonatal Intensive Care Unit between February 2019 and January 2020 (39 children), and who applied to the Physiotherapy and Rehabilitation Department from the centers outside for physiotherapy needs (9 children).
Conditions
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Study Design
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CASE_CONTROL
OTHER
Study Groups
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case
The case group consisted of patients who were diagnosed in the Neonatal Intensive Care Unit (39 children), and who applied to the Physiotherapy and Rehabilitation Department from the centers outside for physiotherapy needs (9 children).
case-control study
physical examination and Survey Form
Control
the children who were at the same age group between the same dates, did not have any diseases related to the neuromuscular system, and hospitalized for any other reason.
case-control study
physical examination and Survey Form
Interventions
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case-control study
physical examination and Survey Form
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
0 Years
2 Years
ALL
No
Sponsors
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Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
OTHER
Responsible Party
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Muhammed ARCA
Dr.
Locations
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University of Health Sciences, Diyarbakır Gazi Yaşargil Training and Research Hospital
Diyarbakır, , Turkey (Türkiye)
Countries
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Other Identifiers
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SBUGaziYasargil21
Identifier Type: -
Identifier Source: org_study_id
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