The goal of this clinical trial is to learn if a low to moderate load power training program is feasible and effective for improving fitness and quality of life of people with prostate cancer under androgen suppression therapy and bone or lymph node metastasis. The main questions it aims to answer are: * Does a low to moderate load power training program improve quality of life in people with metastatic prostate cancer under androgen deprivation therapy? * Does a low to moderate load power training program improve power, strength, endurance, and balance in people with metastatic prostate cancer under androgen deprivation therapy? Researchers will compare the exercise program with routine care to see if power training works to improve common physical side effects of androgen suppression therapy in patients with metastatic prostate cancer. Participants will: * Participate in a supervised exercise program twice a week for 6 months or maintain routine care. * Perform fitness tests and questionnaires about quality of life and mental health. * Those who take part in the exercise program will also perform semi-structured in-depth interviews after the end of the program.
Background and Rationale: Prostate cancer is the most frequently diagnosed cancer among men worldwide, particularly affecting older populations, with increasing incidence and prevalence projected in the coming decades. While survival rates have improved substantially, these advances have not been matched by improvements in long-term quality of life. A significant proportion of patients with advanced prostate cancer undergo androgen deprivation therapy (ADT), which reduces testosterone levels to control tumor progression. Despite its effectiveness, ADT is associated with multiple adverse effects, including loss of muscle mass and strength, increased adiposity, decreased bone mineral density, chronic fatigue, and metabolic alterations. These changes resemble an accelerated aging process and increase the risk of sarcopenia, osteoporosis, and functional dependency. In addition, ADT has been linked to psychological disturbances, including depression, anxiety, cognitive impairment, and reduced vitality. Health-related quality of life (HRQoL) is a multidimensional construct encompassing physical, psychological, and social domains. In prostate cancer patients undergoing ADT, quality of life is significantly impaired due to the combined effects of disease burden and treatment-related side effects. Mental health plays a central role in this construct, as cancer diagnosis and treatment are highly stressful experiences that can disrupt identity, autonomy, and life continuity. Exercise has been identified as an effective non-pharmacological intervention for mitigating many of the adverse effects of ADT. Systematic reviews and meta-analyses have demonstrated that exercise improves muscle strength, cardiorespiratory fitness, functional performance, fatigue, and body composition in this population. Exercise has also been associated with improvements in quality of life and emotional well-being, particularly when interventions are supervised and long-term. The mechanisms underlying these benefits are multifactorial. Neurobiological processes include increased levels of neurotransmitters and brain-derived neurotrophic factor (BDNF), as well as reduced systemic inflammation. From a psychosocial perspective, exercise enhances self-efficacy, perceived control, and social interaction, all of which contribute to improved mental health. However, most existing research has focused on aerobic or traditional resistance training protocols aimed at hypertrophy. There is a lack of studies examining power-oriented resistance training, which emphasizes rapid force production at moderate loads. Muscle power declines more rapidly than strength with aging and is a critical determinant of functional independence. It is particularly relevant for activities of daily living such as standing up, climbing stairs, or maintaining balance. Given that ADT induces an accelerated decline in neuromuscular function, power-oriented training may be especially beneficial in this population. Furthermore, this type of training may use lower loads and avoid excessive fatigue, which may enhance adherence in patients experiencing chronic fatigue. Additionally, previous studies have relied predominantly on quantitative measures, which may not fully capture the subjective and psychosocial dimensions of exercise participation. A mixed-methods approach is therefore necessary to understand how exercise influences identity, motivation, and psychological adaptation in men with prostate cancer. Objectives: Primary Objective 1. To determine the effects of a power-oriented resistance training program on health-related quality of life in older men with metastatic prostate cancer undergoing androgen deprivation therapy. 2. To assess improvements in functional capacity, including strength, balance, and performance in daily activities. Secondary Objectives 1. To evaluate the effects on mental health outcomes, including anxiety, depression, emotional well-being and self-esteem. 2. To determine the safety and feasibility of power-oriented resistance training. 3. To explore participants' subjective experiences using qualitative methods. Hypotheses: 1. The intervention will significantly improve quality of life compared to the control group. 2. Power-oriented resistance training will be safe and well tolerated. 3. Functional capacity will significantly improve following the intervention. 4. Participants will show improved mental health outcomes. 5. Qualitative findings will reveal improvements in self-efficacy, identity, and psychosocial adaptation. Study Design: This study is a randomized controlled trial (RCT) with a mixed-methods approach. Participants will be randomly assigned to: * Experimental Group: Power-Oriented Resistance Training * Control Group: Usual care, with information and guidance on how to be physically active at home. The intervention will last 24 weeks, with a 6-month follow-up. Participants: A total of 66 participants will be recruited, based on power analysis (α = 0.05; power = 0.80; effect size = 0.5). An attrition rate of 20% was also considered. Inclusion Criteria: * Histopathologically confirmed diagnosis of prostate adenocarcinoma. • Metastatic hormone-sensitive prostate cancer (mHSPC), defined as: * Presence of metastases at initial diagnosis (synchronous mHSPC), or * Development of metastatic disease following prior treatment with curative intent (surgery and/or radiotherapy) (metachronous mHSPC). • Evidence of progression to castration-resistant prostate cancer (CRPC). * Ongoing treatment with a doublet regimen consisting of standard androgen deprivation therapy (ADT) in combination with an androgen receptor signaling inhibitor (ARSI), initiated prior to study enrollment. * Receipt of bone-protective therapy, including calcium and vitamin D supplementation in combination with bisphosphonates. * Presence of metastatic involvement limited to bone and/or lymph nodes. * Functionally independent in activities of daily living. Exclusion Criteria: * Evidence of visceral metastatic disease. * Current or prior treatment with a triplet regimen that includes chemotherapy. * History of pathological fracture. Intervention: Power-Oriented Resistance Training • Frequency: 2 sessions/week. * Intensity: 40-50% 1RM. * Execution: High-velocity concentric phase. * Volume: Low to moderate. * No training to failure. This model is designed to improve functional performance while minimizing fatigue and injury risk. Control Group: Participants will receive information and guidance for being physically active and perform strength training at home. Outcome Measures: Primary Outcome • Health-related quality of life (FACT-P). Secondary Outcomes • Functional capacity: (Rate of force development; Handgrip test; Timed up and go test; 6-Minute Walk Test; 10-meter walking speed; 5 times Sit to stand test). • Mental health (anxiety, depression and stress): DASS-21. • Self-esteem: Rosenberg scale. • Physical activity levels: (IPAQ SF). • Adverse events (field diary). Qualitative Analysis • Semi-structured interviews. • Field diaries. • Thematic analysis. This will explore identity, motivation, and adaptation processes associated with exercise participation. Data Analysis • 2 × 2 repeated-measures ANOVA. • Effect size calculations. • Thematic qualitative analysis. Expected Impact. This study will: * Provide novel evidence on power training in prostate cancer. * Inform clinical exercise guidelines. * Improve quality of life and mental health. * Support integration of exercise into oncology care. Conclusion: This randomized controlled trial addresses a key gap in exercise oncology by evaluating a power-oriented resistance training program in men undergoing ADT. By combining quantitative and qualitative approaches, the study aims to provide a comprehensive understanding of both physiological and psychosocial outcomes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
66
The intervention consists of a supervised power-oriented resistance training program for older men with prostate cancer undergoing androgen deprivation therapy (ADT). Participants will complete 2 sessions per week over 24 weeks. Training focuses on improving muscle power through exercises performed at moderate intensity (40-50% 1RM), emphasizing a fast concentric phase and controlled eccentric phase. Multi-joint functional exercises targeting major muscle groups are included to enhance strength, balance, and daily functional performance. Training volume is low-to-moderate, and participants do not train to muscular failure, allowing maintenance of movement velocity and reducing fatigue. Adequate rest periods are provided between sets. The program is adapted to the clinical characteristics of the population, minimizing mechanical stress while promoting neuromuscular improvements. It is designed to be safe, feasible, and well-tolerated, with the aim of improving functional capacity.
University of Alicante
San Vicent del Raspeig, Alicante, Spain
RECRUITINGHealth-related quality of life
Quality of life will be assessed using the Functional Assessment of Cancer Therapy-Prostate (FACT-P) questionnaire. This instrument includes the Functional Assessment of Cancer Therapy-General (FACT-G) and a prostate cancer-specific subscale, providing a multidimensional assessment of physical, social/family, emotional, and functional well-being, as well as prostate cancer-related symptoms and concerns. The total score will be used for analysis, with higher scores indicating better quality of life. Results will be expressed in points, with a score range of 0 to 156. In addition, quality of life will be complemented by a final semi-structured interview exploring participants' perceptions and experiences after the intervention.
Time frame: From enrollment to the end of the exercise program at 6 months.
Rate of Force Development
A test will be conducted to calculate the rate of force development (RFD), defined as the ability of the neuromuscular system to increase contractile force in an optimal and rapid manner when activating a muscle from a low level or from rest. The assessment will be carried out using Chronojump strain gauges (Boscosystem, Spain) during a knee extension exercise at a 90-degree angle. Force (in Newtons) and time (in milliseconds) will be recorded continuously over a 200 ms time window and combined to report RFD in Newtons per second (N/s), calculated as ΔForce/ΔTime. Three 5-second trials will be performed with a one-minute rest between trials, and the mean of the three trials will be used as the single reported value for statistical analysis.
Time frame: From enrollment to the end of the exercise program at 6 months.
Lower-body strength
Lower-body strength will be assessed using the Five Times Sit-to-Stand test. Participants will be instructed to stand up and sit down from a chair five times as quickly as possible, with arms crossed over the chest and without using the upper limbs for assistance. Performance will be recorded as the time required to complete the test, expressed in seconds (s).
Time frame: From enrollment to the end of the exercise program at 6 months.
Handgrip strength
Maximal grip strength will be assessed using a dynamometer (Takei model 5101). Participants will perform two maximal trials with both the dominant and non-dominant hand following the recommendations of the American Society of Hand Therapists). Each contraction will be held for 3 seconds, with a 1-minute rest between trials. The highest value obtained from the two trials will be used for analysis. Results will be expressed in kilogram-force (kgf).
Time frame: From enrollment to the end of the exercise program at 6 months.
Functional mobility
Functional mobility will be assessed using the Timed Up and Go (TUG) test. Participants will stand up from a chair, walk 3 meters, turn around, walk back, and sit down. One familiarization trial will be allowed before the recorded trial. Performance will be recorded as the time required to complete the test, expressed in seconds (s).
Time frame: From enrollment to the end of the exercise program at 6 months.
Gait speed
Gait speed will be assessed using the 10-meter walk test. Participants will perform the test at their maximum safe walking speed without running. In accordance with the study protocol, the central 6 meters will be recorded, using dual-beam photocells positioned at meters 2 and 8 to exclude acceleration and deceleration phases. Results will be expressed in meters per second (m/s).
Time frame: From enrollment to the end of the exercise program at 6 months.
Functional aerobic capacity
Functional exercise capacity will be assessed using the 6-Minute Walk Test. Participants will be instructed to walk as far as possible in 6 minutes along a flat, hard-surfaced standardized course. The total distance covered will be recorded in meters (m).
Time frame: From enrollment to the end of the exercise program at 6 months.
Static balance
Static balance will be assessed by means of a posturographic analysis using a FreeMed baropodometric platform (Rome, Italy). Static balance will be evaluated under eyes-open and eyes-closed conditions in a random order. Participants will perform three 30-second trials for each condition, with 1 minute of rest between trials. The mean of the three trials will be used for analysis. Stabilometric parameters derived from the center of pressure (CoP) will include total excursion, 95% confidence ellipse area, mean velocity, X-Mean, Y-Mean, X-RMS, and Y-RMS. Results will be expressed using center of pressure-derived stabilometric parameters.
Time frame: From enrollment to the end of the exercise program at 6 months.
Mental health
Mental health will be assessed using the Depression Anxiety Stress Scales-21 (DASS-21) questionnaire. This self-report instrument evaluates symptoms of depression, anxiety, and stress experienced over the previous week. The total score and domain scores will be used for analysis, with higher scores indicating greater psychological distress. Results will be expressed in points, with a total score range of 0 to 63 and subscale score ranges of 0 to 21 for depression, anxiety, and stress. In addition, mental health will be complemented by a final semi-structured interview exploring participants' perceptions and experiences after the intervention.
Time frame: From enrollment to the end of the exercise program at 6 months.
Self-esteem
Self-esteem will be assessed using the Rosenberg Self-Esteem Scale (RSES), in its validated Spanish version. This self-report instrument consists of 10 items assessing global self-esteem and self-worth. The total score will be used for analysis, with higher scores indicating higher self-esteem. Results will be expressed in points, with a score range of 10 to 40. In addition, self-esteem will be complemented by a final semi-structured interview exploring participants' perceptions and experiences after the intervention.
Time frame: From enrollment to the end of the exercise program at 6 months.
Physical activity level
Physical activity level will be assessed using the International Physical Activity Questionnaire-Short Form (IPAQ-SF), in its validated Spanish version. This self-administered questionnaire assesses walking, moderate physical activity, vigorous physical activity, and sedentary time over the previous 7 days. Results will be calculated and expressed in MET-minutes per week (MET-min/week). As this questionnaire is used to estimate physical activity volume, it does not have a fixed minimum or maximum total score.
Time frame: From enrollment to the end of the exercise program at 6 months.
Body composition
Body composition will be assessed using a Tanita MC-780-P multi-frequency segmental body composition analyzer. This assessment will provide estimates of body weight, body mass index, body fat percentage, fat mass, fat-free mass, and muscle mass. Results will be expressed in the corresponding units for each parameter.
Time frame: From enrollment to the end of the exercise program at 6 months.
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