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

Last updated: February 13, 2025
Sponsor: Centre Leon Berard
Overall Status: Active - Recruiting

Phase

N/A

Condition

Testicular Cancer

Pain (Pediatric)

Urologic Cancer

Treatment

Physical Activity (PA) Intervention

Physical activity recommendations

Connected activity tracker

Clinical Study ID

NCT05588700
STARTER (ET 22-125)
  • Ages > 18
  • Male

Study 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

Inclusion Criteria:

  • Men ≥18 years

  • With a metastatic germ cell tumor histologically confirmed (seminoma andnon-seminoma)

  • Who have already undergone an orchidectomy

  • 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 amedical certificate issued by the referring oncologist or the investigatingphysician

  • Available and willing to participate in the study for the duration of theintervention and follow-up,

  • Able to understand, read and write French,

  • Affiliated with a social security scheme,

  • Having dated and signed an informed consent.

Exclusion

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 anylocation and/or basal cell skin cancer and/or basal cell skin cancer and/or a cancerin complete remission for more than 3 years),

  • Contraindication to physical activity (e.g. uncontrolled hypertension, uncontrolledheart disease) uncontrolled heart disease),

  • Unable to be followed for medical, social, family, geographical or psychologicalreasons, during the entire study period,

  • Deprived of liberty by judicial or administrative decision, or adults protected bylaw,

  • Concurrent participation in another study in PA.

Study Design

Total Participants: 236
Treatment Group(s): 3
Primary Treatment: Physical Activity (PA) Intervention
Phase:
Study Start date:
January 14, 2025
Estimated Completion Date:
January 14, 2038

Connect with a study center

  • CHU Jean Minjoz

    Besançon, 25030
    France

    Site Not Available

  • Institut Bergonié

    Bordeaux, 33000
    France

    Site Not Available

  • Centre François Baclesse

    Caen, 14076
    France

    Site Not Available

  • Centre Oscar Lambret

    Lille, 59020
    France

    Site Not Available

  • Centre Leon Berard

    Lyon, 69008
    France

    Active - Recruiting

  • Institut de Cancérologie de Lorraine

    Nancy, 54519
    France

    Site Not Available

  • Centre Antoine Lacassagne

    Nice, 06189
    France

    Site Not Available

  • Centre Eugène Marquis

    Rennes, 35000
    France

    Site Not Available

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