RecruitingNot ApplicableNCT05588700

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

A National, Multicenter, Phase III Randomized Controlled Trial to Assess the Impact of a One-year Supervised Physical Activity Program to Reduce Long-term Cancer-related Fatigue in Metastatic Testicular Germ Cell Tumor Patients


Sponsor

Centre Leon Berard

Enrollment

236 participants

Start Date

Jan 14, 2025

Study Type

INTERVENTIONAL

Conditions

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

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a structured physical activity program can reduce long-lasting fatigue in men with testicular cancer that has spread. Many patients experience extreme tiredness after chemotherapy, and researchers want to see if guided exercise during treatment helps prevent this. **You may be eligible if...** - You are a man aged 18 or older with metastatic testicular germ cell tumor (seminoma or non-seminoma) - You have already had surgery to remove the affected testicle - You are about to start a first round of chemotherapy (BEP, EP, or VIP regimens) - You have a smartphone and can use an activity tracker - Your doctor has cleared you for adapted physical activity **You may NOT be eligible if...** - You have bone or brain metastases that cause symptoms - You have nerve damage affecting your ability to walk - You have had another primary cancer (other than skin cancer or a cancer in remission for over 3 years) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALPhysical activity recommendations

At the baseline, all participants will receive the international recommendations in terms of physical activity for promoting health in the general population.

BEHAVIORALConnected activity tracker

At baseline, all participants will receive a connected activity tracker to wear 24 hours a day during one year. Patients will be asked to download an application, dedicated to the study so that the physical activity data (ie. number of steps per day) will be synchronized in the application.

BEHAVIORALPhysical Activity (PA) Intervention

The intervention will last 1 year and will have 2 phases. Phase 1: At each cycle of chemotherapy, patients will be proposed to perform 2-4 sessions per week. This program will be individual, supervised, performed at a moderate intensity. Between cycles, patients will be asked to perform 1-2 supervised collective live online physical activity sessions per week, proposed by a partner specialized in online PA. Phase 2: After chemotherapy, patients will be asked to perform 2-3 PA sessions per week at a moderate intensity. Patients will be offered different options of PA practice: in the supervised collective live online PA session (as already performed in the phase 1), and/or in a fitness center (this practice will take place in a "classic" environment with a 9-month free access for patients thanks to a partnership), and/or self-practice. In addition, patients will benefit from 4 individual motivational interviews, conducted by videoconference and/or by phone call with a professional.


Locations(12)

Institut de Cancérologie de Lorraine

Angers, France

CHU Jean Minjoz

Besançon, France

Institut Bergonié

Bordeaux, France

Centre François Baclesse

Caen, France

Centre Oscar Lambret

Lille, France

Centre Leon Berard

Lyon, France

Institut de Cancérologie de Lorraine

Nancy, France

Centre Antoine Lacassagne

Nice, France

AP-HP Tenon

Paris, France

Centre Eugène Marquis

Rennes, France

CHU Tours

Tours, France

Institut Gustave Roussy

Villejuif, France

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NCT05588700