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Moderate Intensity Intermittent Walking in Postmenopausal Women

W

Wissal Abassi

Status

Completed

Conditions

Liver Enzymes
Inflammatory Markers

Treatments

Behavioral: Walking training intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06809270
Walking and liver function

Details and patient eligibility

About

The goal of this clinical trial is to investigate the impact of a walking training intervention program on liver enzymes and selected inflammatory markers in postmenopausal women with obesity. The main question it aims to answer is:

Does walking training reduce the risk of liver disease by modulating hepatic-enzymes and selected inflammatory markers? Researchers will compare walking training intervention (designed to the experimental group) to non-training intervention (designed to the control group) to see if the training program works to improve liver health in obese postmenopausal women.

Participants in the experimental (training) group will: underwent a moderate intensity intermittent walking training (MIWT) at 60% to 80% of the 6-min-walking-test distance, four times a week of 60 min/session.

Participants in control group will : not perform any physical training and maintain their usual daily activities.

Full description

Postmenopausal obesity is an important public health problem accompanied by increased systemic inflammation that escalates the risk of liver disease. Exercise improved inflammatory and hepatic function. Moderate-intensity intermittent-walking-training (MIWT) is the most feasible for obese-postmenopausal-women. This study aimed to investigate whether MIWT could reduce the risk by modulating hepatic-enzymes and selected inflammatory markers. Thirty-six sedentary obese postmenopausal women (mean age 55.7±3.5) were randomly divided into two groups: training group (TG, n=18) and control group (CG, n=18). The TG underwent a MIWT at 60% to 80% of the 6-min-walking-test distance, four times a week of 60 min/session. Body composition, hepatic (alanine-transaminase (ALT), aspartate-transaminase (AST), alkaline-phosphatase, gamma-glutamyl-transferase (GGT) and serum-bilirubin] and inflammatory markers [C-reactive-protein (CRP), and erythrocyte-sedimentation-rate (ESR)) were evaluated at baseline and after 10-week of protocol.

Enrollment

36 patients

Sex

Female

Ages

50 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Women included are:

  • Postmenopausal (≥1 year of amenorrhea).
  • Obese (body mass index (BMI) ≥30 kg/m2).
  • Sedentary (<120 min/week of low to moderate intensity physical activity at during the past 6 months).
  • Aged 50 to 60 years.

Exclusion criteria

  • Suffering from any cardiovascular/renal/pulmonary/metabolic disease.
  • Being under menopausal hormone therapy.
  • Presenting any orthopedic limitations interfering the ability to perform the study intervention.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

Training group
Experimental group
Description:
The training group underwent a moderate intensity intermittent walking training at 60% to 80% of the 6-min-walking-test distance, four times a week of 60 min/session for a period of 10 weeks.
Treatment:
Behavioral: Walking training intervention
Control group
No Intervention group
Description:
No training intervention was intended for this group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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