- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05935371
Consequences of Obstetric Anal Sphincter Injuries on Maternal Psychology and Relationship Experience (COMPaRE)
The Impact of Severe Perineal Trauma on Maternal Mental Health and Intra-family Relationships
Study Overview
Status
Detailed Description
Obstetric anal sphincter injuries encompass grade 3 and 4 perineal tears and effect the integrity of the anorectal sphincter complex, with or without involvement of the anorectal mucosa. Obstetric anal sphincter injuries occur following a vaginal delivery and are more common in primiparae women, occurring with an incidence in the UK of 6.1% compared to 1.7% in those who are multiparae. Although obstetric anal sphincter injuries is fairly uncommon, the rate of these injuries in singleton, cephalic and first vaginal deliveries, has reportedly tripled from 1.8% to 5.9% from 2000 to 2012. This may, however, be secondary to better detection of these injuries following improvements in education, training and the utilization of a standardized classification system for perineal tears. To address the rising obstetric anal sphincter injury rates, the obstetric anal sphincter injury care bundle was introduced which primarily focused on interventions in the antenatal period to reduce the incidence of these injuries. Prevention of these injuries, however, will not always be possible, even with the best efforts of care. Therefore, focus should also be placed on the optimal management of these patients post-partum. This is especially important as these injuries may be associated with a myriad of devastating and stigmatizing sequelae, including faecal and urinary incontinence, dyspareunia, rectovaginal fistulae, perineal pain and pelvic organ prolapse. It is not surprising, therefore, that sustaining such an injury may impact a woman's decision to have another baby. Severe perineal trauma, with or without complications may, understandably, cause a negative impact on the mental health of afflicted mothers.
Suffering from the complications of these injuries may impact on an individual's quality of life and day-to-day functioning, further augmenting the psychological impact of obstetric anal sphincter injuries. Research has highlighted obstetric anal sphincter injuries to be a risk factor for the development of post traumatic stress disorder symptoms. At present, mothers with these injuries are not routinely screened for these conditions in the post-natal period. Preliminary research has shown that acquiring such an injury negatively affects the relationship between a mother and her child, which invariably has a deleterious effect on a child's development.
This study delivers a questionnaire which incorporates existing, screening tools including the Patient Health Questionnaire-9 (PHQ-9), Generalised Anxiety Disorder-7 (GAD-7), Post-traumatic stress disorder checklist (PCL-5), Rosenberg self-esteem score, Arizona sexual experiences scale, Dyadic Adjustment Scale and the Mother infant bonding scale (MIBS) to assess the impact of these injuries on a women's mental health and intra-family relationships. The PHQ-9 has been shown to be on par with the Edinburgh postnatal depression scale in screening for depression in the perinatal period.
Recognition of mental health dysfunction within this cohort, if present, would facilitate early intervention which may in turn reduce the long-term consequences of a traumatic child birth.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Brent
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London, Brent, United Kingdom, NW107NS
- London Northwest Healthcare NHS Trust
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Contact:
- Sunder CHITA
- Phone Number: 0208 8695829
- Email: sunderchita@nhs.net
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Contact:
- NADA ELSAID
- Email: n.elsaid@nhs.net
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Principal Investigator:
- Carolynne J Vaizey
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Sub-Investigator:
- NADA ELSAID
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Case group - women with obstetric anal sphincter injuries
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Control group - women without perineal tears
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
the impact of an obstetric anal sphincter injury on
Time Frame: study to be completed within 12 months
|
the incidence of depression using the patient health questionnaire-9 screening tool.
The binary outcome cut off is 10 for this questionnaire.
The higher the score the worse the outcome.
Mininum score 0. Maximum score 27.
|
study to be completed within 12 months
|
the impact of an obstetric anal sphincter injury on
Time Frame: study to be completed within 12 months
|
the presence and severity of post-traumatic stress disorder using the post-traumatic stress disorder checklist (PCL-5) screening tool.
Outcome is continuous.
The higher the score, the worse the outcome.
Minimum score 0. Maximum score 80.
|
study to be completed within 12 months
|
the impact of an obstetric anal sphincter injury on
Time Frame: study to be completed within 12 months
|
patient self-esteem using the rosenberg self-esteem scale.
The binary outcome cut off is 15.
Range is 0-30.
Scores below 15 suggest low self esteem.
|
study to be completed within 12 months
|
the impact of an obstetric anal sphincter injury on
Time Frame: study to be completed within 12 months
|
sexual dysfunction (quantifying sex drive, arousal, vaginal lubrication/penile erection, ability to reach and satisfaction from orgasm) using the arizona sexual experiences scale.
Range of score from 5-30.
A total score > or equal to 19 or any 1 item with an individual score of more than or equal to 5 or any 3 items with individual scores of more than or equal to 4 are highly correlated with the presence of sexual dysfunction.
|
study to be completed within 12 months
|
the impact of an obstetric anal sphincter injury on
Time Frame: study to be completed within 12 months
|
quality of a relationship within an intact couple using the abbreviated dyadic adjustment scale (DAS-4).
A score of 14 is the binary outcome cut off.0-21
range.
Higher the score the better the relationship.
|
study to be completed within 12 months
|
the impact of an obstetric anal sphincter injury on
Time Frame: study to be completed within 12 months
|
anxiety using the generalised anxiety disorder-7 screening tool.
The binary outcome cut off is 10.
Range is 0-21.
The higher the score, the greater the anxiety.
|
study to be completed within 12 months
|
the impact of an obstetric anal sphincter injury on
Time Frame: study to be completed within 12 months
|
mother to infant bonding using the mother to infant bonding scale.
Range score 0-24.
The higher the score, the more likely bonding is disrupted.
|
study to be completed within 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The influence of the following factor in predicting severity and risk of mental health disorders and relationship dysfunction (specifically pertaining to relationship with partner and child):
Time Frame: study to be completed over a 12 month period
|
age
|
study to be completed over a 12 month period
|
The influence of the following factor in predicting severity and risk of mental health disorders and relationship dysfunction (specifically pertaining to relationship with partner and child):
Time Frame: study to be completed over a 12 month period
|
type of delivery (e.g.
instrumental/assisted or spontaneous vaginal delivery)
|
study to be completed over a 12 month period
|
The influence of the following factor in predicting severity and risk of mental health disorders and relationship dysfunction (specifically pertaining to relationship with partner and child):
Time Frame: study to be completed over a 12 month period
|
number of vaginal births
|
study to be completed over a 12 month period
|
The influence of the following factor in predicting severity and risk of mental health disorders and relationship dysfunction (specifically pertaining to relationship with partner and child):
Time Frame: study to be completed over a 12 month period
|
history of previous obstetric anal sphincter injury.
The researchers will attempt to obtain this information by reviewing the patient's medical records and asking the patient if they have been previously diagnosed with an obstetric anal sphincter injury.
|
study to be completed over a 12 month period
|
The influence of the following factor in predicting severity and risk of mental health disorders and relationship dysfunction (specifically pertaining to relationship with partner and child):
Time Frame: study to be completed over a 12 month period
|
grade of tear (assessed clinically or radiologically)
|
study to be completed over a 12 month period
|
The influence of the following factor in predicting severity and risk of mental health disorders and relationship dysfunction (specifically pertaining to relationship with partner and child):
Time Frame: study to be completed over a 12 month period
|
Obstetric Anal sphincter Injury (OASI) induced incontinence and severity (as assessed by St Mark's incontinence scale).
St Mark's score ranges from 0-24.
Abnormal is scores more than 5.
The greater the score, the greater the incontinence score.
|
study to be completed over a 12 month period
|
Collaborators and Investigators
Collaborators
Publications and helpful links
General Publications
- Sabourin S, Valois P, Lussier Y. Development and validation of a brief version of the dyadic adjustment scale with a nonparametric item analysis model. Psychol Assess. 2005 Mar;17(1):15-27. doi: 10.1037/1040-3590.17.1.15.
- Skari H, Skreden M, Malt UF, Dalholt M, Ostensen AB, Egeland T, Emblem R. Comparative levels of psychological distress, stress symptoms, depression and anxiety after childbirth--a prospective population-based study of mothers and fathers. BJOG. 2002 Oct;109(10):1154-63. doi: 10.1111/j.1471-0528.2002.00468.x.
- Ertan D, Hingray C, Burlacu E, Sterle A, El-Hage W. Post-traumatic stress disorder following childbirth. BMC Psychiatry. 2021 Mar 16;21(1):155. doi: 10.1186/s12888-021-03158-6.
- Thornton C, Schmied V, Dennis CL, Barnett B, Dahlen HG. Maternal deaths in NSW (2000-2006) from nonmedical causes (suicide and trauma) in the first year following birth. Biomed Res Int. 2013;2013:623743. doi: 10.1155/2013/623743. Epub 2013 Aug 19.
- Garthus-Niegel S, Horsch A, Handtke E, von Soest T, Ayers S, Weidner K, Eberhard-Gran M. The Impact of Postpartum Posttraumatic Stress and Depression Symptoms on Couples' Relationship Satisfaction: A Population-Based Prospective Study. Front Psychol. 2018 Sep 19;9:1728. doi: 10.3389/fpsyg.2018.01728. eCollection 2018.
- Bick Obe D, Hall J, Keighley MRB. The impact of severe perineal trauma on a woman's relationship with her child: a hidden consequence. Midwifery. 2022 May;108:103323. doi: 10.1016/j.midw.2022.103323. Epub 2022 Mar 22. No abstract available.
- Shonkoff M, Duncan GJ, Yoshikawa H, et al. Maternal depression can undermine the development of young children. Centre on the developing child, Harvard University; 2009.
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 327802
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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