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Construction and application of a health promotion behavioral intervention program for infertile patients with polycystic ovary syndrome based on BCW theory

Construction and application of a health promotion behavioral intervention program for infertile patients with polycystic ovary syndrome based on BCW theory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103129
Enrollment
Unknown
Registered
2025-05-26
Start date
2025-05-26
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Polycystic ovaryian syndrome

Interventions

Interventional group:On the basis of the control group, an intervention program based on the BCW theory was implemented.
Qualitative research stage:None

Sponsors

Hangzhou Hospital of Traditional Chinese Medicine Affiliated to Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Qualitative research stage: 1. Meeting the Rotterdam (2003 version) diagnostic criteria for PCOS; 2. Meeting the diagnostic criteria for infertility in the 2019 version of the guidelines; 3. Age >= 20 years old; 4. Having a primary school education or above, with normal language comprehension, expression and communication skills; 5. Voluntary participation and informed consent. Application stage of the protocol (randomized controlled trial): 1. Meeting the Rotterdam (2003 version) diagnostic criteria for PCOS; 2. Meeting the diagnostic criteria for infertility in the 2019 version of the guidelines; 3. Age >= 20 years old; 4. PCOS patients with low or moderate scores on the PCOS Health Promoting Lifestyle Profile; 5. Having a primary school education or above, with normal language comprehension, expression and communication skills; 6. Voluntary participation and informed consent.

Exclusion criteria

Exclusion criteria: Qualitative research stage: 1. Neuro-psychiatric diseases accompanied by severe cognitive dysfunction; 2. Chronic diseases that seriously affect the quality of life of patients, such as malignant tumors, etc.; 3. Intellectual or hearing impairments that prevent cooperation. Application stage of the protocol (randomized controlled trial): 1. Neuro-psychiatric diseases accompanied by severe cognitive dysfunction; 2. Chronic diseases that seriously affect the quality of life of patients, such as malignant tumors, etc.; 3. Infertility caused by male factors, female fallopian tubes, cervix and other factors; 4. Ovulation disorders caused by hyperprolactinemia, premature ovarian failure, etc.; 5. Severe diseases of the cardiovascular and cerebrovascular, liver, kidney, hematopoietic system, etc.; 6. Recent history of major life events.

Design outcomes

Primary

MeasureTime frame
Health Promotion Lifestyle for PCOS Patients;

Secondary

MeasureTime frame
Self-Efficacy ;BMI;Waist hip rate;E2;Progesterone;LH;FSH;Testosterone;PRL;

Countries

China

Contacts

Public ContactYang Jin

Hangzhou Hospital of Traditional Chinese Medicine Affiliated to Zhejiang Chinese Medical University

260918052@qq.com+86 137 7739 8429

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 11, 2026