Screening for Malnutrition and Sarcopenia in Outpatients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a non-interventional, cross-sectional, non-randomized observational screening carried out in outpatient clinics. Adults aged 18 and over who attend medical, radiation oncology, neurology, and geriatrics clinics will be asked to provide informed consent and complete screening procedures at a single visit. No experimental treatments are given and data are collected only to identify risk of malnutrition and sarcopenia. The study is sponsored by Abbott Nutrition and conducted at Necmettin Erbakan University Faculty of Medicine (Meram, Konya).

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Participant has voluntarily signed and dated an informed consent form (ICF), approved by an Independent Ethics Committee (IEC)/Institutional Review Board (IRB), and provided other applicable privacy regulation authorization (if applicable) prior to any participation in the study.
* Participant is ≥ 18 years of age who attend hospital clinics (medical and radiation oncology, neurology, and geriatrics clinics) as an outpatient for any reason.

Exclusion Criteria:

* NA

Where it's running

• Çukurova University Balcalı Hospital General Surgery
  Sarıçam, Adana, Turkey (Türkiye) Recruiting
• Çukurova University Balcalı Hospital Health Practice and Research Center Internal Medicine and Medical Oncology
  Sarıçam, Adana, Turkey (Türkiye) Recruiting
• Ankara University Faculty of Medicine Hospital General Surgery Clinic
  Altındağ, Ankara, Turkey (Türkiye) Recruiting
• Ankara Training and Research Hospital General Surgery Clinic Anesthesia and Reanimation
  Altındağ, Ankara, Turkey (Türkiye) Recruiting
• Ankara Training and Research Hospital Geriatrics Clinic
  Altındağ, Ankara, Turkey (Türkiye) Recruiting
• Ankara Memorial Hospital
  Çankaya, Ankara, Turkey (Türkiye) Recruiting

+19 more sites. See ClinicalTrials.gov for the full list.

Study contacts

• Study coordinator: Kristen DeLuca
• Email: kristen.deluca@abbott.com
• Phone: 614-624-5455

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.