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Not yet recruitingNCT07555457Updated Apr 29, 2026

Intermittent Walking Training and Cardiometabolic Health in Premenopausal and Postmenopausal Women

An interventional study of Moderate-Intensity Intermittent Walking Training (MIWT) in Cardiometabolic Health in Premenopausal and Postmenopausal Women, sponsored by High Institute of Sports and Physical Education of Kef. Not yet recruiting at 1 site in Tunisia. Open to female participants aged 32 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-04-29.

Sponsored by High Institute of Sports and Physical Education of Kef · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
32 Years to 65 Years
Sex
Female
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Cardiometabolic Health in Premenopausal and Postmenopausal Women

Keywords

  • Intermittent walking
  • Premenopausal women
  • Postmenopausal women
  • Cardiometabolic health
  • C-reactive protein
  • Lipid profile
  • Aerobic capacity
03

In context

Lead sponsor

High Institute of Sports and Physical Education of Kef is the lead sponsor of 10 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
32 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Women aged 32 to 43 years (premenopausal, with regular menstrual cycles for at least 12 months) or 49 to 65 years (, with absence of menstruation for at least 12 months).

(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

Exclusion Criteria:

  • Cardiovascular diseases (hypertension, heart failure).
  • Presence of metabolic or inflammatory disorders (e.g., uncontrolled diabetes, diseases, active infections).
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
32 participants (estimated)

Study arms

  • Experimental
    Premenopausal Women Receiving MIWT Program

    Participants in the premenopausal group 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. Body composition, aerobic capacity, heart rate, blood pressure, lipid profile, and C-reactive protein will be assessed before and after the intervention.

    Behavioral: Moderate-Intensity Intermittent Walking Training (MIWT)

  • Experimental
    Postmenopausal Women Receiving MIWT Program

    Participants in the postmenopausal group will perform the same 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. Body composition, aerobic capacity, heart rate, blood pressure, lipid profile, and C-reactive protein will be assessed before and after the intervention.

    Behavioral: Moderate-Intensity Intermittent Walking Training (MIWT)

Interventions

  • BehavioralModerate-Intensity Intermittent Walking Training (MIWT)

    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.

06

What researchers measure

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.

  5. C-Reactive Protein (CRP)

    Serum CRP concentration (mg/L).

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

  6. Total Cholesterol

    Serum total cholesterol concentration (mg/dL).

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

  7. High-Density Lipoprotein (HDL) Cholesterol

    Serum HDL cholesterol concentration (mg/dL).

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

  8. Low-Density Lipoprotein (LDL) Cholesterol

    Serum LDL cholesterol concentration (mg/dL).

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

  9. Triglycerides

    Serum triglyceride concentration (mg/dL).

    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.

07

Study locations

1 site
  • High Institute of Sport and Physical Education of Kef, University of Jendouba
    El Kef, Boulifa 7100, Tunisia
08

References and documents

Individual participant data

Plan to share: No — For confidentiality reasons, all data from this study are available upon request.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for May 2026; primary completion for Aug 2026, 2 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 21, 2026
First posted
Apr 29, 2026
StartEst.
May 21, 2026
Primary completionEst.
Aug 20, 2026
CompletionEst.
Aug 20, 2026
Last update
Apr 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07555457
Lead sponsor
High Institute of Sports and Physical Education of Kef
Responsible party
Wissal Abassi (Dr, High Institute of Sports and Physical Education of Kef) — Principal investigator
First posted
Apr 29, 2026
Start date
May 21, 2026 (estimated)
Primary completion
Aug 20, 2026 (estimated)
Completion
Aug 20, 2026 (estimated)
Last update
Apr 29, 2026

Study contacts

Wissal Abassi Dr
Contact
wissalabassi93@gmail.com
+21693304684
Wissal Abassi
principal investigator · Research Unit "Sport Sciences, Health and Movement"(UR22JS01) High Institute of Sport and Physical Education of Kef, University of Jendouba, 7100 Kef, Tunisia.

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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