Malnutrition Clinical Trials

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Effects of Randomized Controlled Exercise and Nutritional Interventions on Muscle Mass, Volume, Fat Infiltration, and Clinical Outcomes in Patients With Malignant Melanoma Receiving Immunotherapy

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this randomized study is to evaluate whether a six-month program of structured resistance exercise combined with individualized nutritional support can preserve or improve skeletal muscle mass and muscle quality in adults with stage II to IV malignant melanoma who are starting treatment with immune checkpoint inhibitors. Participants will be randomly assigned either to the exercise and nutritional intervention in addition to standard oncology care or to standard oncology care alone. The study aims to obtain complete measurements from at least 40 participants. Assessments will be performed at baseline, after 3 months, and after 6 months. They will include magnetic resonance imaging of the thigh, dual-energy X-ray absorptiometry, bioelectrical impedance analysis, indirect calorimetry, clinical data, and patient-reported outcomes. The study will compare changes in skeletal muscle mass and volume, fatty infiltration of skeletal muscle, sarcopenia, body composition, resting energy expenditure, quality of life, fatigue, treatment tolerance, treatment delays, and early treatment discontinuation between the two groups. Treatment with immune checkpoint inhibitors is provided as part of routine clinical care and is not the investigational intervention.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• Age 18 years or older.

• Confirmed diagnosis of malignant melanoma, stage II, III, or IV.

• Planned first-line or adjuvant treatment with immune checkpoint inhibitors.

• Life expectancy greater than 6 months.

• Sufficient knowledge of the Slovenian language.

• Ability to provide written informed consent and comply with the study protocol.

Locations
Other Locations
Slovenia
Institute of Oncology Ljubljana
RECRUITING
Ljubljana
Contact Information
Primary
Nada Rotovnik Kozjek, MD, PhD
NKozjek@onko-i.si
+38641 612 541
Time Frame
Start Date: 2026-08
Estimated Completion Date: 2029-06
Participants
Target number of participants: 40
Treatments
Experimental: Exercise and Nutritional Intervention
Participants will receive standard oncology care, including treatment with immune checkpoint inhibitors, together with a six-month structured resistance exercise program performed three times per week under the supervision of trained exercise professionals and individualized nutritional support.
No_intervention: Standard Oncology Care
Participants will receive standard oncology care, including treatment with immune checkpoint inhibitors, without the additional structured exercise program or individualized nutritional intervention.
Related Therapeutic Areas
Sponsors
Collaborators: Science and Research Centre Koper
Leads: Institute of Oncology Ljubljana

This content was sourced from clinicaltrials.gov