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Testicular Cancer and Aerobic and Strength Training (TAST)

Primary Purpose

Testicular Neoplasms

Status
Terminated
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Exercise group
Control group
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Testicular Neoplasms focused on measuring Testicular cancer, Physical Exercise, Chemotherapy

Eligibility Criteria

18 Years - 60 Years (Adult)MaleDoes not accept 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

Sites / Locations

  • Oslo University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Exercise group

Control group

Arm Description

Aerobic- and Strength Training program

One lifestyle counseling session

Outcomes

Primary Outcome Measures

VO2peak (directly by modified Balke protocol on a treadmill)
Differences in change in VO2peak from pre- to post-intervention between the exercise group and the control group.

Secondary Outcome Measures

VO2peak (directly by modified Balke protocol on a treadmill)
Differences in change in VO2peak from pre-post-intervention to three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of reduced VO2peak at 12 months follow-up in all participants.
Spirometry
Differences in change in pulmonary function (lung capacity, lung volume, diffusion capacity) from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group.
One-repetition maximum muscle strength test (1RM)
Differences in change in muscle strength from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group.
Dual-energy X-ray absorptiometry (DXA)
Differences in change in lean body mass and fat mass from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of unhealthy body composition at 12 months follow-up in all participants.
Body mass index (BMI)
Differences in change in BMI from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of unhealthy BMI at 12 months follow-up in all participants.
Hip- and Waist circumferences
Differences in change in hip- and waist circumferences from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group.
Godin Leisure Time Exercise Questionnaire (GLTEQ)
Differences in change in physical exercise from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of being inactive at 12 months follow-up in all participants.
Sick leave and Work Ability Index (WAI)
Differences in work ability and sick leave from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of reduced work ability at 12 months follow-up in all participants.
The European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) C-30
Differences in change in health related quality of life (HRQOL) from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of having reduced HRQOL at 12 months follow-up in all participants.
Fatigue questionnaire
Differences in change in fatigue from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of having fatigue at 12 months follow-up in all participants.
Hospital and Anxiety and Depression Scale (HADS)
Differences in change in anxiety and depression from pre- to post-intervention and to three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of having anxiety and depression at 12 months follow-up in all participants.
Markers for inflammation, endothelia dysfunction, thrombosis and cardiovascular diseases and cisplatin
Differences in change in blood tests from pre- to post intervention and at three and 12 months follow-up in the exercise group and the control group. Examine potential risk factors for endothelia dysfunction, activated coagulation and thrombosis and cardiovascular diseases (metabolic syndrome) at 12 months follow-up in all participants.
Safety and tolerability
Number of participants with adverse events during the exercise intervention.

Full Information

First Posted
October 8, 2015
Last Updated
January 25, 2017
Sponsor
Oslo University Hospital
Collaborators
Norwegian School of Sport Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02577172
Brief Title
Testicular Cancer and Aerobic and Strength Training
Acronym
TAST
Official Title
Testicular Cancer and Aerobic and Strength Training - a Randomized Controlled National Phase II Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Terminated
Why Stopped
Unexpected events
Study Start Date
November 2015 (Actual)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Norwegian School of Sport Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Testicular Neoplasms
Keywords
Testicular cancer, Physical Exercise, Chemotherapy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise group
Arm Type
Experimental
Arm Description
Aerobic- and Strength Training program
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
One lifestyle counseling session
Intervention Type
Behavioral
Intervention Name(s)
Exercise group
Intervention Description
The intervention will be conducted during chemotherapy and tailored for each patient. The program will include 1) weight bearing aerobic exercises to maintain the oxygen transport and thereby reduce the decline in VO2max during chemotherapy and 2) strength training exercises to maintain muscle mass and muscle strength. The intervention will last for 9 or 12 weeks, depending on the number of BEP/EP cycles received. The program will consist of two-three one-hour exercise sessions per week, of which most supervised by a personal trainer. The intensity of each exercise sessions will varies from easy (warm-up: 60-70 % of peak heart rate) to moderate/high (between aerobic intervals 60-70% of peak heart rate and during aerobic intervals 85-95 %).
Intervention Type
Behavioral
Intervention Name(s)
Control group
Intervention Description
The control group will receive one individual lifestyle counseling session during the first chemotherapy cycle and can perform all activities that they have planned to do during chemotherapy.
Primary Outcome Measure Information:
Title
VO2peak (directly by modified Balke protocol on a treadmill)
Description
Differences in change in VO2peak from pre- to post-intervention between the exercise group and the control group.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13)
Secondary Outcome Measure Information:
Title
VO2peak (directly by modified Balke protocol on a treadmill)
Description
Differences in change in VO2peak from pre-post-intervention to three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of reduced VO2peak at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Spirometry
Description
Differences in change in pulmonary function (lung capacity, lung volume, diffusion capacity) from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
One-repetition maximum muscle strength test (1RM)
Description
Differences in change in muscle strength from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Dual-energy X-ray absorptiometry (DXA)
Description
Differences in change in lean body mass and fat mass from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of unhealthy body composition at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Body mass index (BMI)
Description
Differences in change in BMI from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of unhealthy BMI at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Hip- and Waist circumferences
Description
Differences in change in hip- and waist circumferences from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Godin Leisure Time Exercise Questionnaire (GLTEQ)
Description
Differences in change in physical exercise from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of being inactive at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Sick leave and Work Ability Index (WAI)
Description
Differences in work ability and sick leave from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of reduced work ability at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
The European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ) C-30
Description
Differences in change in health related quality of life (HRQOL) from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of having reduced HRQOL at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Fatigue questionnaire
Description
Differences in change in fatigue from pre- to post-intervention and at three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of having fatigue at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Hospital and Anxiety and Depression Scale (HADS)
Description
Differences in change in anxiety and depression from pre- to post-intervention and to three and 12 months follow-ups between the exercise group and the control group. Examine potential prognostic factors of having anxiety and depression at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Markers for inflammation, endothelia dysfunction, thrombosis and cardiovascular diseases and cisplatin
Description
Differences in change in blood tests from pre- to post intervention and at three and 12 months follow-up in the exercise group and the control group. Examine potential risk factors for endothelia dysfunction, activated coagulation and thrombosis and cardiovascular diseases (metabolic syndrome) at 12 months follow-up in all participants.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13) and at three and 12 months follow-ups
Title
Safety and tolerability
Description
Number of participants with adverse events during the exercise intervention.
Time Frame
Pre-intervention (week 0) to post-intervention (week 10/13)

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lene Thorsen, PhD
Organizational Affiliation
Oslo University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oslo University Hospital
City
Oslo
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
32525564
Citation
Thorsen L, Haugnes HS, Fossa SD, Brydoy M, Tandstad T, Wisloff T, Gjerset GM, Edvardsen E, Larsen KO, Sandset PM, Henriksson CE, Raastad T, Negaard HFS. Thromboembolic events after high-intensity training during cisplatin-based chemotherapy for testicular cancer: Case reports and review of the literature. Int J Cancer. 2020 Dec 1;147(11):3189-3198. doi: 10.1002/ijc.33151. Epub 2020 Jul 1.
Results Reference
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Testicular Cancer and Aerobic and Strength Training

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