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NCT Number: NCT07555457

Intermittent Walking Training and Cardiometabolic Health in Premenopausal and Postmenopausal Women

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.

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Key information

Age range

32 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

High Institute of Sport and Physical Education of Kef, University of Jendouba

El Kef, Boulifa, 7100, Tunisia

Location contact

Wissal Abassi Dr

CONTACT

[email protected]

+21693304684

About this study

In premenopausal and postmenopausal women, differences in cardiometabolic profile, body composition, and aerobic capacity are commonly observed, with postmenopausal women generally presenting higher cardiometabolic risk. Regular physical activity is known to improve these parameters; however, the specific effects of moderate-intensity intermittent walking training (MIWT) on the comparison between premenopausal and postmenopausal women remain insufficiently explored.

The purpose of this study is to compare the effects of a 10-week moderate-intensity intermittent walking training (MIWT) program on aerobic capacity, body composition, cardiometabolic risk factors, and inflammatory markers in premenopausal and postmenopausal women.

Thirty-two women were allocated into a premenopausal group (n = 16) and a postmenopausal group (n = 16). Both groups performed a MIWT program three times per week for 10 weeks. Each training session consisted 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.

Body composition, aerobic capacity (6MWT), heart rate, blood pressure, lipid profile (total cholesterol, LDL-C, HDL-C, triglycerides), and C-reactive protein (CRP) were assessed before and after the intervention in both groups to evaluate changes induced by the training program.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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).

Body mass index (BMI) > 24.9 kg/m².

  • For the postmenopausal group: amenorrhea ≥ 12 months.
  • For the premenopausal group: regular menstrual cycles for at least 12 months.

Exclusion criteria

  • Cardiovascular diseases (hypertension, heart failure).
  • Presence of metabolic or inflammatory disorders (e.g., uncontrolled diabetes, autoimmune diseases, active infections).

Treatment and study plan

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.

Primary outcomes

  1. Body Mass Index (BMI)

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

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

  2. Body Fat Percentage

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

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

  3. Waist Circumference

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

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

  4. Hip Circumference

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

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

  5. C-Reactive Protein (CRP)

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

    Serum CRP concentration (mg/L).

  6. Total Cholesterol

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

    Serum total cholesterol concentration (mg/dL).

  7. High-Density Lipoprotein (HDL) Cholesterol

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

    Serum HDL cholesterol concentration (mg/dL).

  8. Low-Density Lipoprotein (LDL) Cholesterol

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

    Serum LDL cholesterol concentration (mg/dL).

  9. Triglycerides

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

    Serum triglyceride concentration (mg/dL).

Secondary outcomes

  1. 6-Minute Walk Test (6MWT) Distance

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

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

  2. Blood Pressure (Systolic and Diastolic)

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

    Measured using an automated arm cuff (Omron BP652).

  3. Resting Heart Rate

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

    Measured using automated device (Omron BP652).

Study contacts

Contact information is provided by the study sponsor or research team.

Wissal Abassi Dr

CONTACT

[email protected]

+21693304684

Sponsors and collaborators

Lead sponsor

High Institute of Sports and Physical Education of Kef

Other

Registry information

Official study title

Effects of a 10-Week Moderate-Intensity Intermittent Walking Training Program on Aerobic Capacity, Cardiometabolic Risk Factors, and Inflammatory Markers in Premenopausal and Postmenopausal Women

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 29, 2026
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.