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Effect of Acupuncture and Diet Modification on amenorrheaIN FEMALE ATHLETE TRIAD

Effect of Acupuncture and Diet Modification on Amenorrhea in Female Athlete Triad

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03817827
Enrollment
0
Registered
2019-01-28
Start date
2018-05-05
Completion date
2019-06-30
Last updated
2021-09-08

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

Conditions

Female Athlete Triad

Keywords

sports injury, female athlete triad, acupuncture

Brief summary

The present study will be designed to investigate the effect of acupuncture and diet modification using soy products on amenorrhea in female athlete triad. For this purpose this study will be carried out on sixty female athletes participating gymnastics. They will be recruited from Sports Medicine specialized center in Nasr City, their ages will range from 17 to 25 years old and their BMI will be \< 20 Kg/m2 .

Detailed description

The subjects will be divided into three groups equal in number, matched for measured variable: Group (A): Acupuncture only will be used in this group for 30 minutes, three times per week for twelve weeks. The acupuncture needles were inserted in points located on the abdomen. Group (B): This group will receive only the diet modification contains soy products (phytoestrogen) as 100 milliliter soy milk and 100 grams soy beans daily in the morning as a breakfast alone to ensure its absorption, this dose had been taken for 12 weeks. Group (C): This group will receive both acupuncture therapy for 30 minutes, three times per week for 12 weeks and diet modification contains soy products as 100 milliliter soy milk and 100 grams soy beans daily in the morning for 12 weeks.

Interventions

OTHERAcupuncture

this group will receive Acupuncture for 30 minutes three times per week

DIETARY_SUPPLEMENTDiet supplementary

Diet supplementary with soy product

Sponsors

National Research Centre, Egypt
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
17 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* All patients suffering from athletic amenorrhea. * Their age will be ranged from 17-25 years old. * Their body mass index will be less than 18.5 kg/m2. * No history of previous pregnancies. * No history of any pathological disease causing amenorrhea. * They are medically stable and consented to participate in the study.

Exclusion criteria

* Patients with gynecological diseases that may cause amenorrhea. * Patients using contraceptive pills. * Patients using hormonal treatment. * Patients using induction of ovulation methods. * Patients following any other diet modification method. * Patients who receive any drug with side effect of amenorrhea.

Design outcomes

Primary

MeasureTime frameDescription
follicle stimulating hormonethree monthsBlood sample will be taken from the patient at the beginning of the study and three months later to determine the change of hormone level using Immulite 1000 immunoassay analyzer
Luteinizing hormonethree monthsBlood sample will be taken from the patient at the beginning of the study and three months later to determine the change of hormone level using Immulite 1000 immunoassay analyzer
estradiol 2three monthsBlood sample will be taken from the patient at the beginning of the study and three months later to determine the change of hormone level using Immulite 1000 immunoassay analyzer

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026