Swahili
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)

Exercise and Quality of Life During Androgen Deprivation Therapy

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliKuajiri
Wadhamini
Tampere University Hospital
Washirika
Varalan urheiluopisto

Maneno muhimu

Kikemikali

This study evaluates effects of supervised exercise in reducing adverse effects of hormonal treatment, increasing quality of life and in inducing a long-term change into more active lifestyle in prostate cancer patients on androgen deprivation therapy. All participants will attend a starting lecture at the beginning of the trial, after which they are randomly allocated to attend 3 months of either supervised or non-supervised exercise program. Leisure time activity, quality of life, blood sugar and cholesterol values, and body composition of participants will be evaluated at three time-points; at recruitment, after 12 weeks and after 24 weeks. Effects on quality of life will also be qualitatively evaluated with single- and group interviews.

Maelezo

Androgen deprivation therapy (ADT) is commonly used in management of advanced or recurrent prostate cancer. It also frequently used adjuvant to curative-intent radiation therapy for localized prostate cancer. Low testosterone levels during androgen deprivation commonly cause adverse effects reducing quality of life. Most common adverse effects include fatigue, weight gain, loss of lean muscle mass, hyperglycemia and hypercholesterolemia.

Regular exercise, especially programs involving combination of both aerobic exercise and resistance training has been shown to reduce to reduce adverse effects of ADT on physical functioning and quality of life. It may also improve disease prognosis.

The study compares effects of supervised and unsupervised exercise on plasma lipid parameters (total cholesterol, LDL, HDL and triglycerides) and glucose levels (fasting plasma glucose, glycated hemoglobin), overall quality of life and on average daily exercise activity in men with prostate cancer and under ADT. As secondary outcome we will study effect on continued exercise activity after the intervention, changes in body composition, blood pressure and risk of fractures, castration resistance as well as death due to prostate cancer and due to any cause.

Study hypothesis is that supervised exercise will improve quality of life, lipid and glucose parameters and increase daily exercise activity more that non-supervised exercise. We also expect higher continued exercise activity, greater changes in body composition and blood pressure and lowered risk of fractures and death in the supervised exercise group.

This is a randomized, controlled clinical trial. The study aims to recruit 40 men on ADT for prostate cancer. This will be a pilot study to estimate effect sizes in Finnish population to inform further larger trial.

All participants attend introductory lecture, where a urologist informs them about adverse effects of ADT and positive effects of exercise during ADT, exercise instructor gives advice for training both at home and in the gym and nutritional therapeutist tells about nutrition to overcome adverse effects of ADT and support training.

After the introductory lecture the participants are randomized 1:1 to either the supervised or non-supervised exercise group (Figure). Men in the supervised group participate in progressive group exercise sessions twice a week for total of 12 weeks at the Varala sports academy in Tampere, Finland. Each exercise session includes both aerobic and resistance training targeting all major muscle groups (Additional document I, exercise program). The non-supervised group will exercise independently for 12 weeks according to the instructions given at the introductory lecture. The first control visit will be after this first period of 12 weeks of exercise.

After the first follow-up visit both group will continue non-supervised exercise for 12 weeks, after which the second control visit will be arranged. Special focus on the second control visit is to see how many in each group has been able to carry on active exercising, i.e. has the intervention promoted long-term change in exercise activity.

Both study group will be given Polar wrist activity monitors to be used 24 h/day for the entire course of the study.

All participants are asked to fill validated quality of life surveys EORTC QLQC-30 (overall quality of life) and EORTC QLQC-PR25 (prostate cancer-specific quality of life) at baseline and again at 1st and 2nd control visits. Additionally, qualitative evaluation of quality of life as well as perceived possibilities and obstacles for exercise are evaluated in individual- and group interviews during the study visits. Plasma lipid and glucose parameters, blood pressure and body composition will be measured at each of these visits.

At each visit a separate blood sample is taken and stored for future measurement of biomarkers associated with prostate cancer progression, glucose and lipid metabolism and effects of exercise.

Tarehe

Imethibitishwa Mwisho: 08/31/2019
Iliyowasilishwa Kwanza: 06/26/2018
Uandikishaji uliokadiriwa Uliwasilishwa: 08/06/2019
Iliyotumwa Kwanza: 08/07/2019
Sasisho la Mwisho Liliwasilishwa: 09/09/2019
Sasisho la Mwisho Lilichapishwa: 09/10/2019
Tarehe halisi ya kuanza kwa masomo: 08/14/2019
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 08/14/2020
Tarehe ya Kukamilisha Utafiti: 08/14/2021

Hali au ugonjwa

Prostate Cancer

Uingiliaji / matibabu

Other: Supervised exercise arm

Other: Lecture

Awamu

-

Vikundi vya Arm

MkonoUingiliaji / matibabu
Experimental: Supervised exercise arm
Informational initiation lecture and supervised exercise twice a week for 12 weeks followed by 12 weeks of non-supervised exercise.
Other: Supervised exercise arm
12 weeks of progressive weight training twice a week supervised by a qualified physiotherapist.
Active Comparator: Non-supervised exercise arm
Informational initiation lecture and only non-supervised exercise

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaMale
Hupokea Wajitolea wa AfyaNdio
Vigezo

Inclusion Criteria:

- Undergoing castration treatment for prostate cancer

- Informed consent for the study

Exclusion Criteria:

- Unable to participate in exercise (ECOG 2 or greater)

- High bone fracture risk (as judged by the primary physician)

- Unable to understand spoken and written instructions in Finnish

Matokeo

Hatua za Matokeo ya Msingi

1. Daily total activity [At randomization and twice more at 12 week intervals]

Daily activity as measured by wrist activity monitor worn by the participants at all times during the study. Measured as metabolic equivalents of task (MET) units. Range from 0.9 to 23.

2. Fasting plasma total cholesterol [At randomization and twice more at 12 week intervals]

Value measure in mmol/l

3. Fasting plasma LDL cholesterol [At randomization and twice more at 12 week intervals]

Value measure in mmol/l

4. Fasting plasma HDL cholesterol [At randomization and twice more at 12 week intervals]

Value measure in mmol/l

5. Fasting plasma triglycerides [At randomization and twice more at 12 week intervals]

Value measure in mmol/l

6. Fasting plasma glucose level [At randomization and twice more at 12 week intervals]

Value measured in mmol/l

7. Blood glycated hemoglobin (HbA1C) level [At randomization and twice more at 12 week intervals]

Value measured in mmol/mol

8. Overall quality of life [At randomization and twice more at 12 week intervals]

Score from validated survey EORTC QLQ-C30, score range from 0-100, with 100 denoting the highest quality of life

9. Prostate cancer-specific quality of life [At randomization and twice more at 12 week intervals]

Score from validated survey EORTC QLQ-PR25, score range from 0-100, with 100 denoting the highest quality of life

Hatua za Matokeo ya Sekondari

1. Change in daily activity after the intervention [Measured daily for 12 weeks' time after the intervention]

Change in daily activity of the supervised exercise group after completion of 12 weeks of supervised exercise as measured by wrist activity monitor in MET units, range from 0.9 to 23.

2. Subjective adverse effects of castration treatment [At randomization and twice more at 12 week intervals]

The effect of supervised exercise on subjective adverse effects of castration treatment for prostate cancer. Qualitative assessment in three individual interviews and one group interview. No scaling used as this is a qualitative rather than quantitative end-point

3. Lean body mass [At randomization and twice more at 12 week intervals]

Bioimpedance-based measurement of lean body mass as percentage of total body mass measured with TANITA MC-780 device

4. Muscle mass [At randomization and twice more at 12 week intervals]

Bioimpedance-based measurement of muscle mass as percentage of total body mass measured with TANITA MC-780 device

5. Skeletal mass [At randomization and twice more at 12 week intervals]

Bioimpedance-based measurement of skeletal mass as percentage of total body mass measured with TANITA MC-780 device measured with TANITA MC-780 device

6. Fat mass [At randomization and twice more at 12 week intervals]

Bioimpedance-based measurement of fat mass as percentage of total body mass measured with TANITA MC-780 device measured with TANITA MC-780 device

7. Metabolic age [At randomization and twice more at 12 week intervals]

Metabolic age measured with bioimpedance-based TANITA MC-780 device

8. Systolic blood pressure [At randomization and twice more at 12 week intervals]

Value measured in mmHg

9. Diastolic blood pressure [At randomization and twice more at 12 week intervals]

Value measured in mmHg

Hatua Nyingine za Matokeo

1. Time to castration resistance [Followed yearly for up to 15 years from randomization]

Time to castration resistance as defined by two consecutive rising PSA levels and increase of 50% or more from the nadir. Measured as months between the study recruitment and first record of castration resistance. Information obtained from patient files.

2. Time to death [Followed yearly for up to 15 years from randomization]

Time to death due to any cause. Measured as months between the study recruitment and date of death. Information obtained from patient files and national death certificate registry.

3. Time to prostate cancer death [Followed yearly for up to 15 years from randomization]

Time to death due to prostate cancer. Measured as months between the study recruitment and date of death. Information obtained from patient files and national death certificate registry.

4. Bone fractures [Followed yearly for up to 15 years from randomization]

Occurrence of any bone fracture requiring either conservative or operative management. Information obtained from patient files and national hospital discharge registry. Fracture site and it's management are recorded.

Jiunge na ukurasa
wetu wa facebook

Hifadhidata kamili ya mimea ya dawa inayoungwa mkono na sayansi

  • Inafanya kazi katika lugha 55
  • Uponyaji wa mitishamba unaungwa mkono na sayansi
  • Kutambua mimea kwa picha
  • Ramani ya GPS inayoshirikiana
  • Soma machapisho ya kisayansi yanayohusiana na utafutaji wako
  • Tafuta mimea ya dawa na athari zao
  • Panga maslahi yako na fanya tarehe ya utafiti wa habari, majaribio ya kliniki na ruhusu

Andika dalili au ugonjwa na usome juu ya mimea ambayo inaweza kusaidia, chapa mimea na uone magonjwa na dalili ambazo hutumiwa dhidi yake.
* Habari zote zinategemea utafiti wa kisayansi uliochapishwa

Google Play badgeApp Store badge