Impact of Obstetric Anal Sphincter Injuries on Women's Mental Health and Relationships
The Impact of Severe Perineal Trauma on Maternal Mental Health and Intra-family Relationships
This study looks at how injuries that can happen during childbirth affect women's mental health and relationships with their families.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 87 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | Female |
| Sponsor | London North West Healthcare NHS Trust Academic / other |
| Locations | 1 site (London, Brent) |
| Trial ID | NCT05935371 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the effects of obstetric anal sphincter injuries on women's mental health and their relationships with family members. It focuses on understanding how these injuries, which can occur during vaginal deliveries, may lead to psychological challenges and impact self-esteem. The research seeks to highlight the importance of providing adequate support and care for affected women in the postpartum period to improve their overall well-being and parenting outcomes. By recognizing the long-term consequences of these injuries, the study advocates for ongoing access to help and therapies for women experiencing these issues.
Who should consider this trial
Good fit: Ideal candidates for this study are adult women aged 18 and older who have experienced a vaginal delivery, regardless of whether they are primiparous or multiparous.
Not a fit: Patients who have had a caesarean section or are unable to consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved mental health support and relationship outcomes for women suffering from obstetric anal sphincter injuries.
How similar studies have performed: While the specific focus on the psychological and relational impacts of obstetric anal sphincter injuries may be novel, related studies have shown the importance of addressing mental health in postpartum care.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * as aforementioned previously * Adult women who have had a vaginal delivery * ≥ 18 years * Capacity to consent * English-speaking * Primiparous/multi-parous Exclusion Criteria: * Women who have had a caesarean section * Women who are unable to consent * Patient who do not speak English
Where this trial is running
London, Brent
- London Northwest Healthcare NHS Trust — London, Brent, United Kingdom (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.