Intermittent Walking Training and Cardiometabolic Health in Premenopausal and Postmenopausal Women

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age32-65
SponsorHigh Institute of Sports and Physical Education of Kef

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Moderate-Intensity Intermittent Walking Training (MIWT)

    Behavioral

    Participants 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

32 Participants
are divided into 2 treatment groups
Group A: Premenopausal Women Receiving MIWT ProgramExperimental treatment 1 intervention
Group B: Postmenopausal Women Receiving MIWT ProgramExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Body Mass Index (BMI)

BMI calculated as weight (kg) divided by height squared (m²).

Time frame
Baseline and after the 10 weeks of the training intervention.
2

Body Fat Percentage

Total body fat measured by digital scale (Tanita BC-533).

Time frame
Baseline and after the 10 weeks of the training intervention.
3

Waist Circumference

Measured at the narrowest point between the rib cage and iliac crest using a tape measure.

Time frame
Baseline and after the 10 weeks of the training intervention.
4

Hip Circumference

Measured at the widest point of the hips using a tape measure.

Time frame
Baseline and after the 10 weeks of the training intervention.

Secondary outcomes

1

6-Minute Walk Test (6MWT) Distance

Distance walked in 6 minutes on a 30-meter straight corridor.

Time frame
Baseline and after the 10 weeks of the training intervention.
2

Blood Pressure (Systolic and Diastolic)

Measured using an automated arm cuff (Omron BP652).

Time frame
Baseline and after the 10 weeks of the training intervention.
3

Resting Heart Rate

Measured using automated device (Omron BP652).

Time frame
Baseline and after the 10 weeks of the training intervention.

Other outcomes

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