Actively Recruiting

Age: 18Years +
All Genders
ID07130981

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Did not provide written informed consent
  • Patients deemed unsuitable by the physician

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

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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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