About this trial
The goal of this clinical trial is to compare premenopausal and postmenopausal women regarding the effects of a 10-week moderate-intensity intermittent walking training (MIWT) program on aerobic capacity and selected cardiometabolic and inflammatory markers. The main question it aims to answer is: Does a MIWT program induce differential improvements in aerobic capacity, body composition, lipid profile, and inflammatory markers between premenopausal and postmenopausal women?
Participants in the premenopausal group will perform a 10-week MIWT program, three sessions per week. Participants in the postmenopausal group will perform the same 10-week MIWT program, three sessions per week. Each training session consists of 5 repetitions of 6-minute walking (6MWT) at 60-80% of the baseline 6MWT distance, interspersed by 6 minutes of active recovery between repetitions. Body composition, aerobic capacity (6-minute walk test), heart rate, blood pressure, lipid profile (total cholesterol, LDL-C, HDL-C, triglycerides), and C-reactive protein (CRP) will be assessed before and after the intervention in both groups.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Women aged 32 to 43 years (premenopausal, with regular menstrual cycles for at least 12 months) or 49 to 65 years (postmenopausal, with absence of menstruation for at least 12 months).
For the postmenopausal group: amenorrhea ≥ 12 months.
For the premenopausal group: regular menstrual cycles for at least 12 months.
Disqualifiers
Cardiovascular diseases (hypertension, heart failure).
Presence of metabolic or inflammatory disorders (e.g., uncontrolled diabetes, autoimmune diseases, active infections).
Trial design
Parallel
Treatments tested in this trial
Moderate-Intensity Intermittent Walking Training (MIWT)
BehavioralParticipants will perform a 10-week moderate-intensity intermittent walking training (MIWT) program, with three supervised sessions per week. Each session consists of 5 repetitions of 6-minute walking (6-minute walk test, 6MWT) performed at 60-80% of the baseline 6MWT distance, interspersed by 6 minutes of active recovery between repetitions. The same intervention is applied to both premenopausal and postmenopausal women.
Treatment groups
Trial outcomes
Primary outcomes
Body Mass Index (BMI)
BMI calculated as weight (kg) divided by height squared (m²).
Body Fat Percentage
Total body fat measured by digital scale (Tanita BC-533).
Waist Circumference
Measured at the narrowest point between the rib cage and iliac crest using a tape measure.
Hip Circumference
Measured at the widest point of the hips using a tape measure.
Secondary outcomes
6-Minute Walk Test (6MWT) Distance
Distance walked in 6 minutes on a 30-meter straight corridor.
Blood Pressure (Systolic and Diastolic)
Measured using an automated arm cuff (Omron BP652).
Resting Heart Rate
Measured using automated device (Omron BP652).
Sponsors and contacts
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