The purpose of this study is to determine whether sustainable daily physical activity is effective in improving biological indicators of health and self-reported quality of life in men with prostate cancer.
Living with prostate cancer is a unique challenge faced by millions of men across the globe. Existing research has indicated many potential methods of attenuating prostate cancer progression and preserving patients' quality of life, but is lacking in definitive conclusions regarding the effectiveness of these methods in practice. This study seeks to further investigate the impact of post-diagnosis physical activity on biological indicators of health and self-reported quality of life in a cohort of men with prostate cancer in Sweden. Participants are randomized to either a walking intervention group, which encourages walking 10,000 steps per day for one year, or to a standard-or-care control group, and followed for 11 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Enrollment
42
Participants are provided with the current standard of prostate cancer care, and are additionally encouraged to walk 10,000 steps per day, as measured by pedometers provided at start of intervention. Once a week, participants will take part in a group walk with 7-8 other participants and a research nurse. Participants are also encouraged to keep a walking journal, in which they record the number of steps they walk each day. This journal is submitted to investigators at the end of the intervention period.
Participants are provided with the current standard of prostate cancer care, but are not assigned to a physical activity intervention.
Orebro University
Örebro, Narke, Sweden
C-Reactive Protein
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
High-Density Lipoprotein
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Adiponectin
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Total Cholesterol
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Triglycerides
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Insulin
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Testosterone
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
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Estradiol
Levels assessed in blood. Blood draw performed by clinician at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Self-Reported Stress
Self-reported stress level measured using the Perceived Stress Scale-4. Questionnaire completed by participant at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Self-Reported Sleep Quality
Self-reported sleep quality measured using the Karolinska Sleepiness Scale. Questionnaire completed by participant at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Self-Reported Emotional Quality of Life
Self-reported emotional quality of life using the 21-Item Depression Anxiety Stress Scale, DASS-21. Questionnaire completed by participant at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Self-Reported Physical Quality of Life
Self-reported physical quality of life measures related to urinary, bowel, and sexual function using the FACT-P questionnaire. Questionnaire completed by participant at start and 11 weeks after start of intervention.
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks
Blodpressur, systolic and diastolic.
Blodpressur systolic and diastolic, will be assesed by the clinican at randomisation and after 11 weeks
Time frame: At time of randomisation(March 1, 2010) and after 11 weeks