About this trial
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.
Eligibility criteria
Qualifiers
Couples who are undergoing their first or second IVF/ICSI cycle;
Couples diagnosed with female-factor infertility;
Couples who have signed consent.
Disqualifiers
Couples who receive donated oocytes, sperm, or embryos;
Couples diagnosed with severe male-factor infertility or unexplained infertility.
Couples who are undergoing Preimplantation Genetic Testing (PGT);
Couples who have not undergone embryo transfer within six months after oocyte retrieval;
Trial design
Treatments tested in this trial
- Gender-transformative intervention
Treatment groups
Sponsors and collaborators
Peking University Third Hospital
Lead sponsor
Beijing Obstetrics and Gynecology Hospital
Collaborator