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the effect of Modified Intermittent Fasting on PMS and Quality of Life in wome

Not Applicable
Conditions
premenstrual syndrome.
Registration Number
IRCT20220522054958N1
Lead Sponsor
Kashan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Women in the age range of 18 to 50 years
Their body mass index is more than or equal to 25 and less than 40
Menstrual bleeding lasting between 3 and 8 days, and normal menstrual cycles of 21–35 days
Having PMS based on PSST (premenstrual symptoms screening tool)
To comply with the study methods

Exclusion Criteria

Pregnancy
Breastfeeding
A history of any chronic diseases such as hypertension, heart disease, diabetes, gastrointestinal disorders such as gastritis, gastric and duodenal ulcers
The habit of smoking
Alcohol abuse
Weight loss of more than1 to 2 kg in the past month
Adherence to a special diet, and medication use in the last 2 months
Taking dietary supplements to lose weight
Mental or psychiatric disorders such as depression
Clinically diagnosed diseases such as infectious, cancer, kidney, CVD, liver, neurological, endocrine, and gynecological diseases
Having surgery in the last 6 months
Enduring extreme stress during the trial
Taking antidepressants and contraceptives
Taking B6 supplements in the past 3 months
Not completing the questionnaire for 3 successive days and 5 non-successive days

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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