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RecruitingLast updated: 25 November 2025

EXHIBIT: This study is assessing how safe and feasible an exercise program alongside immunotherapy treatment is for people diagnosed with melanomaThe safety and feasibility of exercise in patients with melanoma undergoing adjuvant immunotherapy with immune checkpoint inhibitor therapy – the EXHIBIT Study

Trial purpose

Medical clipboardCancer treatment; Side effect and wellbeing

Tumor type

Skin Cancers Skin

Age

People18+

Trial acronym

EXHIBIT

Clinical summary

Summary

You may be eligible for this study if you are aged 18 years or over, have a diagnosis of cutaneous melanoma and are scheduled to receive adjuvant immune checkpoint inhibitor (ICI) immunotherapy treatment.

Eligible participants will be randomly allocated to either an exercise intervention or standard medical care.

Participants randomised to the exercise group will receive a structured exercise intervention for the duration of their ICI immunotherapy treatment (approximately 12 months). The intervention will involve 3 exercise sessions per week (45-60minutes per session) involving both supervised and unsupervised exercise sessions.

Participants randomised to the control group will receive usual medical care and general exercise advice as per the current exercise oncology guidelines. 

All participants will be asked to complete a variety of questionnaires, undergo fitness testing, and provide blood samples. 

It is hoped that findings from this study will inform researchers of the effect of exercise concurrent to ICI immunotherapy, following surgery, for patients with melanoma. 

Conditions

This trial is treating people with cutaneous melanoma who have had surgery and are scheduled to receive adjuvant immune checkpoint inhibitor immunotherapy treatment

Eligibility

Inclusion

 

Diagnosis of cutaneous melanoma
Scheduled to receive adjuvant immune checkpoint inhibitor immunotherapy treatment
Greater than or equal to 18 years of age
ECOG performance status less than or equal to 2
Ability and willingness to travel for the study visits and adhere to the exercise intervention
Written informed consent.

Exclusion

 

Stage IV/metastatic disease
Received neoadjuvant immunotherapy
Received greater than 1 immunotherapy infusion
Receiving treatment for another cancer (excluding non-melanoma skin cancer)
Currently performing equal to or more than 150 mins of moderate to vigorous intensity intentional physical activity per week
Serious active infection; severe neurologic or cardiac impairment according to ACSM criteria
Any contraindications for exercise as determined by the treating clinician
Any circumstances that would impede adherence to study requirements or ability to give informed consent, as determined by the treating clinician
Pregnant

Inclusion

  • Your cancer has not spread to other parts of the body (localised).
  • You have the type of cancer, symptoms, or health risks that this clinical trial is focused on.

Exclusion

  • You have certain types of non-cancer medical conditions.
  • You have had certain treatments, surgical procedures or drugs.
Message

Clinical trials have complex eligibility criteria, and other criteria may apply for this trial. Ask your doctor about whether this trial could be right for you.

Participating hospitals

Recruiting hospitals

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More information

Trial Identifiers

Information on this page is partially produced from ANZCTR *. View further details about this trial on the registry via the links below:

Trial sponsor

Australian Catholic University

Scientific Title

The safety and feasibility of exercise in patients with melanoma undergoing adjuvant immunotherapy with immune checkpoint inhibitor therapy – the EXHIBIT Study

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