Actively Recruiting
Melatonin Supplementation and Exercise Program in Breast Cancer Women
Led by University of Valladolid · Updated on 2024-11-20
120
Participants Needed
1
Research Sites
67 weeks
Total Duration
On this page
Sponsors
U
University of Valladolid
Lead Sponsor
S
Sanidad de Castilla y León
Collaborating Sponsor
AI-Summary
What this Trial Is About
Introduction: Breast cancer (BC) remains the leading cause of cancer in women with nearly 1.4 million new cases worldwide annually and 27.000 in Spain. Increasingly effective oncology therapies, however, have numerous adverse effects such as muscle degeneration, fatigue, decreased physical function and aerobic capacity, and deteriorating quality of life. In this sense, physical activity (PA) seems to be an interesting non-pharmacological strategy to alleviate these serious complications and with potential benefits for women with BC. Melatonin (N-acetyl-5 methoxytryptamine) is an indolic compound present with pleiotropic bioactions that regulates the circadian rhythm, antioxidant, anti-inflammatory, immunostimulant, cardioprotective, antidiabetic, antiobesity, neuroprotective, and antiaging actions. Furthermore, in recent years, many studies have described the key role of melatonin in preventing and developing cancer. The general anticarcinogenic mechanisms include epigenetic control, cell proliferation modulation, cell cycle regulation, apoptosis induction, and telomerase inhibition. Melatonin also exerts antiestrogenic activity, which is particularly significant in hormone-dependent tumors, regulating the expression and transactivation of the estrogen receptor, and modulating the enzymes involved in the local synthesis of estrogens. Despite all the mentioned properties, the use of melatonin in daily clinical practice is very limited, and additional studies are needed to better establish the role of this hormone in oncological clinical applications against different types of cancer. Objective: To analyze the effect of supplementation with 4 g/day of melatonin for 10 weeks on muscle damage (CK and LDH), hormonal responses (estradiol, testosterone, cortisol and testosterone/cortisol ratio), antioxidant capacity (BAP and d-ROMs), Exerkins (Irisin and Sestrin 2), physical performance (handgrip strength, RPE and SPPB), anthropometry (body mass, BMI and fat mass) and WHOQOL-BREF (physical and psychological health, social relationships and environment) in women over 60 years of age who have suffered breast cancer and who follow a physical training program. Methods: A total of 20 female volunteers between 60 and 73 years old (age: 65.5±4.52 years, BMI: 25.83±2.67 and body fat percentage: 33.73±5.54) who followed a physical activity adapted to their age and abilities are the members. of this study. The volunteers were divided into two groups: placebo (CG; n = 10) and supplemented with 5 g/day of melatonin (GI; n = 10). Differtent test were performed muscle damage (CK, and LDH), hormonal responses (estradiol, testosterone, cortisol, and testosterone/cortisol ratio), antioxidant capacity (BAP and d-ROMs), Exerkins (Irisin and Sestrin 2), physical performance (Hand-grip strength, RPE and SPPB), anthropometrics (Body mass, BMI and fat mass), and WHOQOL-BREF (physical and psychological health, social relationships and environment) were analyzed at the beginning (T1) and at the end of the 10 weeks of intervention (T2).
CONDITIONS
Official Title
Melatonin Supplementation and Exercise Program in Breast Cancer Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women with a history of ductal carcinoma in situ, lobular carcinoma in situ, or stage 1 to 3 breast cancer diagnosed 5 or more years ago
- Not currently receiving chemotherapy or hormone therapy
- Postmenopausal women
- Eastern Cooperative Oncology Group (ECOG) score of 1 or less
- Women aged between 60 and 80 years
- Ability to participate in a physical training program adapted to age and abilities
You will not qualify if you...
- Women who exercised regularly for at least 20 minutes twice a week or more in the 3 months before the study
- Stage IV breast cancer or systemic recurrences
- Known autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis, or multiple sclerosis
- Severe kidney disease
- Use of adjuvant hormonal therapy, oral estrogen or progesterone replacement therapy, or luteinizing hormone-releasing hormone agonists currently or within the past 60 days
- Less than 6 months post-chemotherapy
- Regular use of sleeping pills every night at bedtime
- Use of black cohosh, flaxseed, or soy supplements
- Functional limitations according to Barthel scale less than 100 or Lawton-Brody scale less than 8
- Uncontrolled hypertension (above 180/100 mm Hg)
- Uncontrolled heart rhythm disorders, severe aortic stenosis, acute endocarditis or pericarditis
- Acute thromboembolic disease
- Moderate to severe chronic obstructive pulmonary disease (Bodex index C or D)
- Recent bone fracture within the last month
- Any condition preventing physical activity as determined by a doctor
- Neoadjuvant chemotherapy or radiotherapy
- Concomitant use of beta-blockers
- Less than 6 months post-radiotherapy
- Concomitant use of postmenopausal hormone replacement therapy
- Use of oral melatonin supplements in the past 30 days
- Acute or chronic heart failure with NYHA score greater than II
- Uncontrolled orthostatic hypotension
- Recent acute myocardial infarction (3 to 6 months) or unstable angina
- Acute or chronic respiratory failure
- Diabetes with acute decompensation or uncontrolled hypoglycemia
- History of dementia
- Shift work or night work
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Trial Site Locations
Total: 1 location
1
Faculty of Health Sciences, University of Valladolid Soria Campus
Soria, Soria, Spain, 42004
Actively Recruiting
Research Team
D
Diego Fernández Lázaro, Professor; PhD
CONTACT
C
Cesar Ignacio Fernández Lázaro, Professor; PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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