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A validation study of a dietary program delivered by family nurses in patients with overweight/obesity and infertility

A validation study of a dietary program delivered by family nurses in patients with overweight/obesity and infertility

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128311
Enrollment
Unknown
Registered
2026-07-17
Start date
2025-08-25
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Infertility

Interventions

Regular diet group:Regular diet receiving health education
Diet therapy group:Family nurse diet therapy program based on the Theory of Family Nurse Diet Therapy

Sponsors

The first hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Overweight or obese (24 = 28 kg/m^2); 2. Age between 20 and 40 years old (including 20 and 40 years old); 3. There is no organic disease in the reproductive system; 4. No related treatment was performed within 3 months, and no hormone drugs were used; 5. Male reproductive function is normal; 6. Volunteered to participate in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Does not meet the diagnosis and inclusion criteria of this disease; 2. Infertility caused by organic diseases such as congenital physiological defects or malformations, bilateral fallopian tube obstruction, pituitary tumors, etc.; 3. Patients diagnosed as endometriosis, adenomyosis, uterine fibroids; 4. Infertility due to male reproductive factors; 5. Follicular dysplasia due to premature ovarian failure; 6. Patients with severe primary diseases of other systems or with mental disorders; 7. Drugs (such as contraceptives, glucocorticoids, etc.) that could affect the results of this trial were taken in the past 3 months; 8. Those who refused to sign informed consent and could not return to the clinic regularly; 9. Allergic to test product ingredients (buckwheat, soybeans, etc.).

Design outcomes

Primary

MeasureTime frame
Body weight;Clinical pregnancy rate;Glucose and lipid metabolism markers;Inflammatory markers;Oxidative stress markers;Cardiovascular disease risk prediction markers;Liver and kidney function markers;

Countries

China

Contacts

Public ContactHan Shifan

The first hospital of Shanxi Medical University

13903409675@139.com+86 351 4639626

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026