Hand Grip Strength and Prognosis in Hospitalized Cancer Patients
PRO-HAND
Hospitalized Cancer Patients: Prognostic Value of Hand Grip Strength - A Prospective Cohort Study
1 other identifier
observational
130
1 country
1
Brief Summary
This prospective cohort study aims to investigate the relationship between hand grip strength and prognosis in hospitalized cancer patients. Hand grip strength, a simple, rapid, and non-invasive measure of overall muscle function, is increasingly recognized as an indicator of frailty, nutritional status, and physical health. The study will evaluate whether lower hand grip strength is associated with higher short-term mortality (30-day all-cause mortality) and adverse clinical outcomes, including ICU admission, hospital readmission, and functional decline.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 25, 2025
CompletedFirst Submitted
Initial submission to the registry
August 23, 2025
CompletedFirst Posted
Study publicly available on registry
September 11, 2025
CompletedSeptember 11, 2025
September 1, 2025
2 months
August 23, 2025
September 3, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
30-day All-Cause Mortality
All-cause mortality within 30 days of hospital admission among cancer patients (Yes/No). Mortality status will be assessed through hospital records and follow-up. Hand grip strength values will be analyzed in relation to mortality risk.
30 days after hospital admission
Secondary Outcomes (6)
Intensive Care Unit Admission
30 days after hospital admission
Hospital Readmission
30 days after discharge
Functional Decline - ECOG Performance Status
Baseline and 30 days after hospital admission
Length of Hospital Stay
Through initial hospitalization, up to 30 days
Major Complications
30 days after hospital admission
- +1 more secondary outcomes
Study Arms (1)
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.
Interventions
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
The study population consists of adult patients aged 18 years and older with pathologically confirmed cancer who are admitted to the Ankara Etlik City Hospital, Department of Medical Oncology. Eligible participants are hospitalized for more than 48 hours and undergo hand grip strength measurement within 24 hours of admission. Patients represent a heterogeneous group of solid tumor cases across different cancer types and stages, reflecting a real-world hospitalized oncology population.
You may qualify if:
- Adults aged 18 years and older
- Pathologically confirmed diagnosis of cancer
- Hospitalized with an expected hospital stay of more than 48 hours
- Ability to provide written informed consent
You may not qualify if:
- Diagnosis of anorexia nervosa
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Etlik City Hospital, Medical Oncology Department
Ankara, Yenimahalle, 06210, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Galip Can Uyar, MD
Ankara Etlik City Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Medical Oncologist, Department of Medical Oncology
Study Record Dates
First Submitted
August 23, 2025
First Posted
September 11, 2025
Study Start
September 1, 2024
Primary Completion
October 20, 2024
Study Completion
March 25, 2025
Last Updated
September 11, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share