Validity and Reliability of 6-minute Pegboard and Ring Test
NCT ID: NCT06943040
Last Updated: 2025-04-24
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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NOT_YET_RECRUITING
34 participants
OBSERVATIONAL
2025-04-28
2025-08-15
Brief Summary
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Detailed Description
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Secondary complications that occur in the short and long term following SCI play an important role in the continuity of care of individuals with SCI. According to the data of the National SCI Statistics Center (NSCISC), complications such as pneumonia, atelectasis, deep vein thrombosis, pulmonary embolism, pressure ulcers, autonomic dysreflexia, renal problems, and fractures are very common after SCI. It is thought that these complications resulting from SCI are a direct result of immobility. In addition, physical inactivity causes loss of functional independence, decreases quality of life, and significantly affects social participation. The daily life of individuals with SCI often consists of low activity levels and leads loss of physical condition. Therefore, the participation of individuals with SCI in exercise and improvement of cardiovascular health and function is necessary to increase life expectancy and quality. Various upper extremity exercises have been shown to improve the general condition of individuals with SCI. Determination of upper extremity strength, endurance, and exercise capacity in individuals with SCI is an important issue in the management of SCI. One of the tests that serves this purpose is the six-minute pegboard and ring test (6PBRT), which is valid and reliable in individuals with chronic obstructive pulmonary disease. Since 6PBRT is used in clinical and research applications in individuals with SCI, it is important to know its validity and reliability. This study aims to investigate the validity and reliability of 6PBRT in individuals with SCI.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Study group
There will be no intervention on the participants within the scope of this study.
There will be no intervention on the participants within the scope of this study.
Interventions
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There will be no intervention on the participants within the scope of this study.
There will be no intervention on the participants within the scope of this study.
Eligibility Criteria
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Inclusion Criteria
* Being an adult (≥18 years old)
* Injury level between T1 and L5
* Being a full-time wheelchair (WD) user for mobility
Exclusion Criteria
18 Years
70 Years
ALL
No
Sponsors
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Istinye University
OTHER
Responsible Party
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Yunus Emre Tutuneken
PhD
Other Identifiers
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1111
Identifier Type: -
Identifier Source: org_study_id
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