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First Time Mothers and Anal Incontinence Six Years Postpartum

First Time Mothers and Anal Incontinence Six Years Postpartum

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02792244
Acronym
FiTMAI6
Enrollment
800
Registered
2016-06-07
Start date
2016-08-31
Completion date
2017-08-31
Last updated
2017-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fecal Incontinence, Quality of Life, Urinary Incontinence

Brief summary

Previous studies show that incontinence is relatively common during pregnancy and after delivery. Experiencing incontinence during pregnancy or in the first year after delivery increases the risk of long term incontinence. There is scarce documentation of the long term prevalence of anal incontinence (AI) in Norway. This study aims to explore prevalence and risk factors for incontinence approximately six years after delivery among the 1718 who participated in two previous studies exploring the prevalence and predictors of anal incontinence in late pregnancy and during the first year after first delivery, and the effect of pelvic floor muscle exercises as treatment for anal incontinence after delivery. Increased awareness and knowledge about risk factors and long term prevalence of anal incontinence among health professionals as well as pregnant and parous women may give indications about which women to target for preventative measures to reduce the risk of new onset of postpartum AI during pregnancy and after delivery. Further, increased knowledge may aid in planning individualized follow-up during pregnancy and the first year as well as in the long term among women with existing AI symptoms.

Interventions

None listed

Sponsors

St.Olavs Hospital, Trondheim University Hospital, Norway
CollaboratorUNKNOWN
Norwegian University of Science and Technology
CollaboratorOTHER
Ostfold Hospital Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Participants in previous studies

Exclusion criteria

* Women not participating in previous studies

Design outcomes

Primary

MeasureTime frameDescription
Anal incontinenceAnal incontinence six years postpartumSt. Mark's score measuring frequency and severity of anal incontinence

Secondary

MeasureTime frameDescription
Urinary incontinenceurinary incontinence six years postpartumICI-Q UI SF measuring frequency and severity of urinary incontinence

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026