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Recruiting NCT05588700

NCT05588700 Impact of a Physical Activity Program to Reduce Long-term Cancer-related Fatigue in Metastatic Testicular Germ Cell Tumor Patients

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Clinical Trial Summary
NCT ID NCT05588700
Status Recruiting
Phase
Sponsor Centre Leon Berard
Condition Metastatic Testicular Cancer
Study Type INTERVENTIONAL
Enrollment 236 participants
Start Date 2025-01-14
Primary Completion 2031-01-14

Eligibility & Interventions

Sex Male only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Physical activity recommendationsConnected activity trackerPhysical Activity (PA) Intervention

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 236 participants in total. It began in 2025-01-14 with a primary completion date of 2031-01-14.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Testicular germ cell tumor (TGCT) is the most common malignancy in men between 15 and 40 years. Although TCGT survivors have a good survival prognosis, they suffer from short- and long-term sequelae such as chronic fatigue, psychological disorders, cardiovascular toxicities and second malignancies. The benefits of physical activity (PA) during treatments have been demonstrated in cancer patients to improve quality of life (QoL) and physical fitness and to reduce fatigue. However, few PA programs have been proposed to TGCT patients and their effects on sequelae have not been assessed yet. A growing body of evidence links treatment-related alteration in the gut microbiota to sequelae of cancer survivors, including fatigue and cardiovascular toxicities. Also, PA has been known as a possible modulator of the gut microbiota composition. To date, no study has been conducted to examine how the gut microbiota and its metabolites moderate the effect of PA on fatigue and other late effects in TGCT survivors. The objectives will be to assess the impact of a PA program on fatigue and other sequelae and to investigate how the gut microbiota and its metabolites moderate the associations between PA and sequelae. We will conduct a prospective, multicenter, phase III, randomized controlled trial of a one-year supervised PA program. 236 men with metastatic TGCT and eligible for a first line of chemotherapy will be randomly assigned to either PA intervention or control arm. All patients will benefit from a connected activity tracker and PA recommendations. In the intervention arm, PA will be based on supervised sessions and motivational interviews. The primary endpoint (fatigue) will be assessed at 3 years. The trial will provide novel insights into the impact of PA on fatigue and other sequelae in TGCT survivors with understanding a potential underlying mechanism of gut microbiota. This evidence will support the development of targeted PA guidelines to improve QoL and reduce sequelae in TGCT survivors.

Eligibility Criteria

Inclusion Criteria: * Men ≥18 years * With a metastatic germ cell tumor histologically confirmed (seminoma and non-seminoma) * Who have already undergone an orchidectomy (since the 16th december, this criteria was deleted). * Having a first line of chemotherapy planned with BEP, EP or VIP * Having a smartphone (i.e. to connect the activity tracker) * PS \< or = 2 * Whose ability to practice an adapted physical activity (APA) has been certified by a medical certificate issued by the referring oncologist or the investigating physician * Available and willing to participate in the study for the duration of the intervention and follow-up, * Able to understand, read and write French, * Affiliated with a social security scheme, * Having dated and signed an informed consent. Exclusion Criteria: * Presence of symptomatic bone and/or brain metastases * Central nervous system involvement with neurological deficits preventing walking * History or coexistence of another primary cancer (apart from in situ cancer of any location and/or basal cell skin cancer and/or basal cell skin cancer and/or a cancer in complete remission for more than 3 years), * Contraindication to physical activity (e.g. uncontrolled hypertension, uncontrolled heart disease) uncontrolled heart disease), * Unable to be followed for medical, social, family, geographical or psychological reasons, during the entire study period, * Deprived of liberty by judicial or administrative decision, or adults protected by law, * Concurrent participation in another study in PA.

Contact & Investigator

Central Contact

Carmen Dupuis, PhD

✉ carmen.dupuis@lyon.unicancer.fr

📞 0469856218

Principal Investigator

Aude Fléchon, MD

PRINCIPAL INVESTIGATOR

Centre Leon Berard

Frequently Asked Questions

Who can join the NCT05588700 clinical trial?

This trial is open to male participants only, aged 18 Years or older, studying Metastatic Testicular Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05588700 currently recruiting?

Yes, NCT05588700 is actively recruiting participants. Contact the research team at carmen.dupuis@lyon.unicancer.fr for enrollment information.

Where is the NCT05588700 trial being conducted?

This trial is being conducted at Angers, France, Besançon, France, Bordeaux, France, Caen, France and 8 additional locations.

Who is sponsoring the NCT05588700 clinical trial?

NCT05588700 is sponsored by Centre Leon Berard. The principal investigator is Aude Fléchon, MD at Centre Leon Berard. The trial plans to enroll 236 participants.

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