Hand Grip Strength and Prognosis in Hospitalized Cancer Patients
NCT ID: NCT07167082
Last Updated: 2025-09-11
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
130 participants
OBSERVATIONAL
2024-09-01
2025-03-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Hospitalized Cancer Patients
This cohort consists of adult patients (aged 18-80 years) with pathologically confirmed cancer who are admitted to the hospital for at least 48 hours. Hand grip strength is measured within the first 24 hours of admission using a standardized dynamometer protocol. Patients are followed prospectively for 30 days to evaluate primary and secondary outcomes including all-cause mortality, functional decline, hospital stay duration, readmission, and major complications.
Hand Grip Strength Measurement
Hand grip strength will be measured within the first 24 hours of hospitalization using a calibrated hand dynamometer. Measurements will be performed on the dominant hand, with patients seated, following standardized international procedures. Three consecutive measurements will be obtained, and the average value will be recorded. The test is non-invasive, quick, and performed by oncology clinicians trained in the protocol.
Interventions
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Hand Grip Strength Measurement
Hand grip strength will be measured within the first 24 hours of hospitalization using a calibrated hand dynamometer. Measurements will be performed on the dominant hand, with patients seated, following standardized international procedures. Three consecutive measurements will be obtained, and the average value will be recorded. The test is non-invasive, quick, and performed by oncology clinicians trained in the protocol.
Eligibility Criteria
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Inclusion Criteria
* Pathologically confirmed diagnosis of cancer
* Hospitalized with an expected hospital stay of more than 48 hours
* Ability to provide written informed consent
Exclusion Criteria
* Acute pancreatitis or acute liver failure at admission
* History of gastric bypass surgery
* Presence of chronic active infections
* History of solid organ transplantation
* Pregnant or breastfeeding women
18 Years
ALL
No
Sponsors
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Ankara Etlik City Hospital
OTHER_GOV
Responsible Party
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Galip Can Uyar
Medical Oncologist, Department of Medical Oncology
Principal Investigators
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Galip Can Uyar, MD
Role: PRINCIPAL_INVESTIGATOR
Ankara Etlik City Hospital
Locations
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Etlik City Hospital, Medical Oncology Department
Ankara, Yenimahalle, Turkey (Türkiye)
Countries
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Other Identifiers
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AEŞH-BADEK-2024-1105
Identifier Type: OTHER
Identifier Source: secondary_id
AEŞH-BADEK-2024-1105
Identifier Type: -
Identifier Source: org_study_id
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