Clinical trial

Physical Activity and Cardiometabolic Health in Women With or Without Polycystic Ovary Syndrome (SCOPAP)

Opening soon · Not applicable · 1 countries · Registry ID NCT07659392

Opening soonNot applicableInterventional

What this study is about

The primary objective of this study is to investigate the effects of a multidisciplinary intervention, including a targeted adapted physical activity program, on lipid oxidation during a walking exercise in women with overweight or obesity, with or without polycystic ovary syndrome. Specifically, the study aims to compare changes in lipid oxidation before and after the intervention between women with polycystic ovary syndrome and those without polycystic ovary syndrome. The secondary objectives are to assess the impact of polycystic ovary syndrome on several physiological and metabolic parameters in women with overweight or obesity. These include: (i) resting energy metabolism; (ii) resting blood pressure and heart rate; (iii) energy expenditure, energy cost, and heart rate during a walking exercise; (iv) body composition, glycemic and lipid profiles, and circulating levels of sex hormones and adipokines; (v) movement behaviors; and (vi) physical fitness. In addition, the effect of the multidisciplinary intervention, including the adapted physical activity program, will be evaluated on these same outcomes: (i) resting energy metabolism; (ii) resting blood pressure and heart rate; (iii) energy expenditure, energy cost, and heart rate during walking exercise; (iv) body composition, glycemic and lipid profiles, and concentrations of sex hormones and adipokines; (v) movement behaviors; and (vi) physical fitness, in women with overweight or obesity, with or without polycystic ovary syndrome.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 40 Years

SexFemale

Healthy volunteersNot accepted

ConditionPoly Cystic Ovary Syndrome, Overweight , Obesity

Full registry criteria

Inclusion Criteria: * Women aged 18 to 40 years (inclusive boundaries) * Women with a body mass index (BMI) between 25 and 40 kg/m² * Women performing no more than 150 minutes of moderate-to-vigorous physical activity per week * Women able to provide informed consent to participate * Women affiliated with a social security system * One group will consist of women with polycystic ovary syndrome, and another group will consist of women without polycystic ovary syndrome Exclusion Criteria: * Pregnancy or breastfeeding, as declared by the participant * Postmenopausal women * Women currently receiving pharmacological treatment for obesity or who have received such treatment within the past two years * Women under legal protection measures (guardianship, curatorship, or judicial protection) * Refusal to sign the informed consent form

Treatments and study arms

Physical activity

Behavioral

Participants will participate to adapted physical activity, supervised by a professional

Primary outcomes

Lipid oxidation during walking exerciseBaseline and after 10 weeks of intervention

Study locations

1 locations were listed when this page was built. The first 40 are shown.

CHU de Clermont-Ferrand🇫🇷 Clermont-Ferrand, France

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Lise LaclautreContact

Email · Call +33473754963