Actively Recruiting
Cardiometabolic Adaptations to Concurrent Training: Effect of Effort Configuration on Postmenopausal Women
Led by Universidade da Coruña · Updated on 2026-04-28
60
Participants Needed
1
Research Sites
134 weeks
Total Duration
On this page
Sponsors
U
Universidade da Coruña
Lead Sponsor
M
Ministerio de Ciencia e Innovación, Spain
Collaborating Sponsor
AI-Summary
What this Trial Is About
The main objectives of this project are to assess the effects of a 20-week concurrent training program on neuromuscular adaptations, body composition, cardiometabolic health, quality of life, mood state, physical self-perception, and menopause-related symptoms in physically active postmenopausal women, and to compare the adaptations resulting from different combinations of endurance and resistance training programs with varying effort configurations. Additionally, this project aims to examine the longitudinal interaction and potential interference effects between endurance and resistance training effort configurations throughout the training program and to determine the optimal combination of effort configurations that maximizes health benefits in concurrent training programs for physically active postmenopausal women.
CONDITIONS
Official Title
Cardiometabolic Adaptations to Concurrent Training: Effect of Effort Configuration on Postmenopausal Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least one year since the last menstrual period.
- Physically active, defined as engaging in 150-300 minutes of moderate physical activity per week or at least 75 minutes of vigorous activity per week.
- Three or fewer traditional cardiovascular risk factors.
- Asymptomatic and without cardiovascular (except controlled hypertension), metabolic, or renal diseases.
- In the case of hypertensive participants, well-controlled grade 1 hypertension managed with a single medication.
You will not qualify if you...
- Diagnosis of grade 2 or grade 3 hypertension.
- Hypertension managed with more than one medication or with a drug that could interfere with cardiovascular responses to exercise (e.g., beta-blockers).
- Current or prior use of hormone replacement therapy.
- Hypertensive response to exercise.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Faculty of Sport Sciences and Physical Education - UDC
Oleiros, A Coruña, Spain, 1517
Actively Recruiting
Research Team
E
Eliseo Iglesias-Soler, PhD
CONTACT
M
María Rúa-Alonso, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
6
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