UnknownNot Applicable

Consequences of Obstetric Anal Sphincter Injuries on Maternal Psychology and Relationship Experience

United Kingdom87 participantsStarted 2023-10-26

Plain-language summary

The aim is to ascertain whether sustaining an Obstetric Anal Sphincter Injury negatively impacts intra-family relationships and increases the risk of mental health conditions, including a women's perception of herself and her self-esteem. Research in this field will ensure that the correct care and adequate support is provided for these patients in the post-natal period and beyond. Recognition of these conditions and the provision of support for these patients may improve relationships, leading to improved parenting and positive outcomes for the child. It ought to be highlighted that the sequelae of obstetric anal sphincter injuries, including anal incontinence, may manifest later on in the female life course and therefore life-long accessibility to help and therapies is advocated for these women.

Who can participate

Age range

18 Years – 60 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

Trial details

NCT IDNCT05935371

SponsorLondon North West Healthcare NHS Trust

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-10

View on ClinicalTrials.gov More Obstetric Complication trials

Plain-language summary

Who can participate

Age range

18 Years – 60 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months

the impact of an obstetric anal sphincter injury on

Timeframe: study to be completed within 12 months