Actively Recruiting
Effects of Normobaric Hypoxia Exercise Program on Bone Turnover Markers and Metabolism in Premenopausal Women
Led by University School of Physical Education, Krakow, Poland · Updated on 2024-05-08
60
Participants Needed
2
Research Sites
134 weeks
Total Duration
On this page
Sponsors
U
University School of Physical Education, Krakow, Poland
Lead Sponsor
M
Ministry of Education and Science,Poland
Collaborating Sponsor
AI-Summary
What this Trial Is About
The impact of a proprietary training program in normobaric hypoxia on changes in bone turnover markers as well as carbohydrate and lipid metabolism in premenopausal women falls within the realm of physical culture for an active and healthy society. Within this context, the implementation of a project is supported aiming to: 1. Monitor, support, and promote physical development, fitness, and physical activity in society, by assessing the effects of a proprietary training program in normobaric hypoxia on changes in bone turnover markers as well as carbohydrate and lipid metabolism in premenopausal women. 2. Develop and implement innovative methods, forms, and means of physical activation and training for individuals of various ages, by formulating general assumptions of an endurance-strength training concept under normobaric hypoxia conditions, concerning changes in bone turnover markers as well as carbohydrate and lipid metabolism in premenopausal women. 3. Prevent injuries in physical education and sports, by designing a useful training program for osteoporosis prevention as well as for managing carbohydrate and lipid metabolism disorders in premenopausal women.
CONDITIONS
Official Title
Effects of Normobaric Hypoxia Exercise Program on Bone Turnover Markers and Metabolism in Premenopausal Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female aged 50 to 59 years
- No significant cardiovascular, respiratory, or musculoskeletal diseases
- No contraindications to physical activity confirmed by ECG, urinalysis, and blood morphology
- T-score within normal limits (+1.0 to -1.0) for bone density
- Provided informed consent to participate in the study
You will not qualify if you...
- Use of hormone replacement therapy (HRT)
- Use of cigarettes or alcohol
- Participation in any training, including hypoxia training or exposure, in the 6 months prior to the intervention
- Any other factors deemed unsuitable by the study investigators
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University School of Physical Education in Cracow
Krakow, Poland, 31-571
Not Yet Recruiting
2
University School of Physical Education in Cracow
Krakow, Poland, 31-571
Actively Recruiting
Research Team
A
Anna Radoń, MSc
CONTACT
M
Małgorzata Bagińska, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
4
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