Actively Recruiting
Evaluation of Body Composition, Psychosocial Factors, and Drug-Related Problems in Relation to Clinical Progression in Cancer Patients Receiving Immune Checkpoint Inhibitors
Led by Hacettepe University · Updated on 2025-08-24
200
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how body composition, psychosocial factors, and drug-related problems affect clinical outcomes in cancer patients treated with immune checkpoint inhibitors. The study aims to understand how these factors relate to toxicity, treatment response, and quality of life during immunotherapy. It is an observational research led by Hacettepe University. Participants will be observed over a maximum of 6 months following the start of immune checkpoint inhibitor treatment. The study will assess body composition using CT scans taken before treatment, evaluate cachexia and psychosocial factors, and monitor drug-related problems throughout the follow-up period. No experimental treatments are administered, as this is an observational study. During the study, participants will undergo evaluations including body composition analysis, psychosocial assessments, and monitoring of drug-related issues. These assessments will help researchers measure clinical progression such as treatment toxicity and response along with quality of life. The total participation time is up to 6 months, during which data will be collected to better understand factors influencing outcomes in patients receiving immunotherapy.
CONDITIONS
Brief Title
Body Composition and Psychosocial Factors in ICI-Treated Cancer Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years or older
- Have undergone a CT scan at the L3 level before treatment
- No severe mental disorder and able to communicate effectively
- Provided written informed consent
You will not qualify if you...
- Did not provide written informed consent
- Patients deemed unsuitable by the physician
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 6 months
Participants are observed with evaluations of body composition, psychosocial factors, and drug-related problems during their cancer treatment with immune checkpoint inhibitors.
Regular assessments during treatment as per clinical care
Trial Site Locations
Total: 1 location
1
Hacettepe University Faculty of Pharmacy, Department of Clinical Pharmacy
Ankara, Altındağ, Turkey (Türkiye), 06100
Actively Recruiting
Research Team
İ
İzgi BAYRAKTAR, PhD (c)- Lecturer
A
Aygin Ekincioglu, Prof.Dr. -Head of department
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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