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Testicular Cancer and Aerobic and Strength Training (TAST)

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Terminated

Conditions

Testicular Neoplasms

Treatments

Behavioral: Exercise group
Behavioral: Control group

Study type

Interventional

Funder types

Other

Identifiers

NCT02577172
REK - 2014/1169

Details and patient eligibility

About

The present study examine the effects of an aerobic and strength training program on cardiorespiratory fitness in testicular cancer (TC) patients during chemotherapy. Half of the participants will receive the exercise program and the other half will receive one individual lifestyle counseling session. The investigators hypothesize that TC patients in the exercise group will have less reduction in cardiorespiratory fitness during chemotherapy treatment compared to patients in the control group.

Full description

Testicular cancer (TC) patients receiving chemotherapy often experience troublesome side-effects during and after treatment. Both aerobic and strength exercise have showed beneficial effects on side-effects during and after treatment in other cancer diagnosis. Knowledge of the effects of physical exercise during and after chemotherapy in TC patients is insufficient and studies are needed. The primary aim is to examine the effects of physical exercise on cardiorespiratory fitness in TC patients during chemotherapy. Secondary aims are to examine the effects of physical exercise on other secondary health outcomes during and three and twelve months after chemotherapy.

The present study is a randomized controlled trial comparing a tailored exercise program consisting of aerobic and strength training during chemotherapy to a control group receiving one individual lifestyle counseling session during the first chemotherapy cycle. The TC patients will be included and assessed before the first cycle of chemotherapy and further assigned to either a exercise group or a control group. The intervention will last for 9 or 12 weeks (depending on the number of bleomycin, etoposide, cisplatin (BEP)/etoposide, cisplatin (EP) cycles received) and it will consists of two-three one-hour sessions per week mostly supervised by a personal trainer. All variables will be assessed pre- and post-intervention, and at three and 12 months follow-up.

Enrollment

19 patients

Sex

Male

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • testicular cancer with seminoma or non-seminoma
  • stage II-IV
  • referred to chemotherapy (3-4 BEP (bleomycin, etoposide and cisplatin)-cycles or 4 EP (etoposide and cisplatin) -cycles) with/without retroperitoneal lymph node dissection (RPLND)
  • satisfactory Norwegian Language skills
  • signed informed consent

Exclusion criteria

  • severe brain and lung metastasis (reduced lung function)
  • heart and lung diseases that contraindicate exercise testing and the supervised exercise program without adjusted actions according to American College of Sports Medicine (ACSM)'s guidelines)
  • physical and mental conditions of a severity that complicates the ability for exercise testing and the supervised exercise program

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

19 participants in 2 patient groups

Exercise group
Experimental group
Description:
Aerobic- and Strength Training program
Treatment:
Behavioral: Exercise group
Control group
Active Comparator group
Description:
One lifestyle counseling session
Treatment:
Behavioral: Control group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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