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Study identifier: NCT06124950 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Couple-based Gender-transformative Intervention on IPV Against Infertile Women

Condition: Infertility, Female · Violence, Domestic  ·  Sponsor: Peking University Third Hospital

PhaseNA
Planned participants752
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a multicenter, open-label, randomized controlled trial conducted at two reproductive medicine centers in Beijing, China. Couples undergoing their first or second in-vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) cycle, diagnosed with female-factor infertility, and who have signed informed consent will be enrolled. Exclusion criteria include couples receiving donated oocytes, sperm, or embryos; those diagnosed with severe male-factor infertility or unexplained infertility; those undergoing preimplantation genetic testing (PGT); those who have not undergone embryo transfer within six months after oocyte retrieval; those with severe mental disorders; and those who withdraw from the study. Participants are will randomly allocated 1:1 by center to either the intervention or control group. Couples in the intervention group will receive five 60-minutes GTI sessions focusing on gender norms, gender equality, and healthy relationship skills, conducted by trained healthcare providers and social workers. The control group will receive standard reproductive care. A total of 376 infertile couples will be enrolled (188 couples per group). The primary outcome is the IPV rate against infertile women over the past 12 months.

This description comes directly from the study's public registry record.

Talk to the study team

Yu Fu, MS  ·  +86 13521777668  ·  annyfy0417@gmail.com

Yuanyuan Wang, Dr  ·  +86 13811352300  ·  yyuanwang@163.com

Always discuss trial participation with your own doctor first.

Locations (2)

Beijing Obstetrics and Gynecology HospitalBeijing, ChinaNot Yet Recruiting
Peking University Third HospitalBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06124950