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Completed

NCT Number: NCT05859789

EFFECT OF MEDITERRANEAN DIET ON SEXUAL FUNCTION IN WOMEN WITH METABOLIC SYNDROME

Metabolic syndrome (MS) is a cluster of metabolic abnormalities that includes hypertension, central obesity, insulin resistance, type 2-diabetes and atherogenic dyslipidaemia (1). A woman's sexual health is associated with several psychological and interpersonal factors, and may be affected by aging and metabolic changes (2).

Obesity, hypertension, dyslipidemia, and type 2-diabetes which are conditions frequently present in women with metabolic syndrome are considered risk factors for atherosclerosis and endothelial dysfunction which impairs tissue oxygenation and causes subsequent functional and structural damage to the female genital tract. A decrease in pelvic blood flow secondary to atherosclerotic disease leads to fibrosis of the vaginal wall and clitoral smooth muscle, eventually resulting in vaginal dryness and dyspareunia (3).

Women with metabolic syndrome showed higher prevalence of sexual inactivity and low sexual desire, orgasm, satisfaction, and Female sexual function (FSFI) total score in respect to women without metabolic syndrome (4). There is a link between diet and sexual performance markers to get and maintain lubrication, orgasm, and frequency of sex, as food has a favourable or negative impact on sexual activity for both sexes at any age (5). The Mediterranean diet (Med Diet) is one of the most widely described and evaluated dietary patterns in scientific literature. It is based on the traditional foods that people used to eat in countries bordering the Mediterranean Sea, including France, Spain, Greece, and Italy. It is characterized by high intakes of vegetables, legumes, fruits, nuts, grains, fish, seafood, extra virgin olive oil, and a moderate intake of red wine (6). Previous studies proved that Kegel exercise raise the level of sexual satisfaction, as the pelvic floor muscle (PFM) specifically the pubococcygeus and iliococcygeus muscles are responsible for the rhythmic involuntary contractions during orgasm (7).

According to the authors' knowledge, no prior research studied the effect of Mediterranean diet on sexual function in women with metabolic syndrome.

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Key information

Age range

25 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Egypt , Giza

Giza, Egypt

About this study

200 patients with metabolic syndrome complaining of sexual dysfunction, aged 25-40 years, were randomized into two equal groups, the control group (A) received sessions of Kegel exercise three times per week for 12 weeks, the study group (B) received Kegel exercise combined with Mediterranean diet regimen for 12 weeks. Female sexual function index (FSFI) questionnaire was used to evaluate sexual function of each woman in both groups, while sexual quality of life-female (SQOL_F) questionnaire was used to assess quality of life (QoL) of each woman in both groups before and after treatment.

All women will be included in this study if they fulfill the following criteria:

  • Sexually active women diagnosed with metabolic syndrome and complaining of sexual dysfunction:
  • Abdominal adiposity (waist circumference is >88 cm)
  • Low serum high density lipoprotein cholesterol
  • Hypertriglyceridemia (elevated triglyceride of >150 mg/dl)
  • Elevated blood pressure >130/85mmHg
  • Abnormal glucose homeostasis (fasting plasma glucose concentration is >110mg/dl).
  • Their age will range (25- 35 ) years
  • Body mass index (BMI) ≥ (25-30) kg/m2.

Women who had met one of the following criteria will be excluded from the study:

  • Women has cardiovascular disease
  • Psychiatric problems
  • History of alcohol abuse
  • Smoker women
  • Taking medication

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

All women will be included in this study if they fulfill the following criteria:

  • Sexually active women diagnosed with metabolic syndrome and complaining of sexual dysfunction:
  • Abdominal adiposity (waist circumference is >88 cm)
  • Low serum high density lipoprotein cholesterol
  • Hypertriglyceridemia (elevated triglyceride of >150 mg/dl)
  • Elevated blood pressure >130/85mmHg
  • Abnormal glucose homeostasis (fasting plasma glucose concentration is >110mg/dl).
  • Their age will range (25- 35 ) years
  • Body mass index (BMI) ≥ (25-30) kg/m2.

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Exclusion criteria

Women who had met one of the following criteria will be excluded from the study:

  • Women has cardiovascular disease
  • Psychiatric problems
  • History of alcohol abuse
  • Smoker women
  • Taking medication

Treatment and study plan

kegel exercise

Procedure
  • Each female will be asked to "Try to squeeze her pelvic floor muscles as much as possible". She was instructed that the numbers she saw at the top of screen indicated the activity of the muscle (electrical activity), in microvolt (mv).
  • The therapeutic session will be repeated 3 sessions /week for 12 weeks for each female in both groups (A&B).
  • Each female will be instructed to Tighten her pelvic floor muscles. Hold tight and count 3 to 5 seconds, relax the muscles and count 3 to 5 seconds, then repeat 10 times, 3 times a day at least three sets of 10 to 15 repetitions a day as a home program
  • They will be instructed not to use abdomen, thighs or buttock muscles during the contraction, avoid holding breath. Instead, breathe freely during the exercises.

Mediterranean diet regimen for 12 weeks.

Other

kegel ex in addition to mediterrian diet . The recommended composition of the dietary regimen was the following: carbohydrates 50-60%, proteins 15-20%, total fat o30%, saturated fat 10% and less than 300 mg of cholesterol consumed per day. Moreover, subjects Will be advised to consume at least 250-300 g of fruits, 125-150 g of vegetables and 25-50 g of nuts per day.

Primary outcomes

  1. Female sexual function index (FSFI) questionnaire

    Time frame: up to 12 weeks

  2. Sexual Quality of Life Questionnaire- Female

    Time frame: up to 12 weeks

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
May 16, 2023
Registry last updated
May 16, 2023

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.