Investigate of anisum consumption on anthropometric indicators of infertile women

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240712062400N1

Enrollment

Registered

2024-08-19

Start date

2024-08-22

Completion date

Unknown

Last updated

2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Investigating the effect of anise consumption on weight loss and anthropometric indicators of women with polycystic ovary syndrome.

Interventions

Intervention 1: Intervention group: They receive 5 grams of anise powder half an hour before lunch and dinner for 8 weeks. Intervention 2: Control group: They receive 5 grams of placebo (corn starch)

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Diagnosis of polycystic syndrome by gynecologist based on Rotterdam criteria Body mass more than 25 Consent to participate in the study

Exclusion criteria

Exclusion criteria: Having diabetes Taking weight loss drugs Participating in intervention studies at the same timeCommunity Verified icon Suffering from severe acute and chronic physical diseasesCommunity Verified icon

Design outcomes

Primary

Measure	Time frame
Weight. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: sinker.;Height. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Round abdomen. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Round the hips. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Round the wrist. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Appetite. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: Visual Analogue Scale.;Physical activity. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: questionnaire.;Quality of life. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: questionnaire.	—

Measure

Time frame

Weight. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: sinker.;Height. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Round abdomen. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Round the hips. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Round the wrist. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: meter.;Appetite. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: Visual Analogue Scale.;Physical activity. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: questionnaire.;Quality of life. Timepoint: Before starting the intervention and after 8 weeks (completion of the study). Method of measurement: questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactShaqayeq Fakhrian

Sabzevar University of Medical Sciences

shaqayeqfakhrian@gmail.com+98 51 4263 2943

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026