Condition 1: Sexual function. Condition 2: Sexual satisfaction. Condition 3: Sexual quality of life.
Conditions
Interventions
Intervention 1: Intervention group: Overweight women will be contacted and, if eligible, invited to participate in the study. After providing full explanations and obtaining informed consent, particip
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 49 Years
Inclusion criteria
Inclusion criteria: Being Iranian. Consent to participate in the study and complete the informed consent form. Educational level at least reading and writing. Being in the reproductive age (ages 15 to 49). Married and sexually active. Have a body mass index of 25-30 kg/m2.
Exclusion criteria
Exclusion criteria: Being on a special diet for losing weight. Being in prenancy or breastfeeding period. Specific diseases such as (hypothyroidism, hyperthyroidism, diabetes, multiple sclerosis, and cancer) or known mental illnesses in women and their husbands (according to the participants' statement). Sexual dysfunction, such as erectile dysfunction or ejaculation disorder in their spouse (according to the participants' statement). Taking drugs that affect sexual activity (such as sildenafil/hormones) in women and their husbands (according to the participants' statement). Taking medications that affect weight status, such as medications that affect carbohydrate, protein, or fat metabolism and medications that reduce appetite or food intake. Smoking, drinking alcohol, or substance abuse in women and their husbands (according to the participants' statement).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual function. Timepoint: Before the intervention and 4 weeks after the intervention. Method of measurement: Female sexual function index.;?Sexual satisfaction. Timepoint: Before the intervention and 4 weeks after the intervention. Method of measurement: Index of Sexual Satisfaction (ISS).;Sexual quality of life. Timepoint: Before the intervention and 4 weeks after the intervention. Method of measurement: Sexual QualityOf life Questionnaire- female (SQOL-F). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Jalali Chimeh
Shahid Beheshti University of Medical Sciences
Outcome results
None listed