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Membrane Sweeping as an Induction Method and Maternal Experience: a Phenomenological Qualitative Study

Membrane Sweeping as an Induction Method and Maternal Experience: a Phenomenological Qualitative Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07154862
Acronym
Sweep
Enrollment
20
Registered
2025-09-04
Start date
2025-02-13
Completion date
2025-05-14
Last updated
2025-09-10

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

Conditions

Labour, Induced, Membrane Stripping, Patient Experience, Phenomenology

Brief summary

This qualitative phenomenological study explores women's experiences with membrane sweeping, a common mechanical method of labor induction. Membrane sweeping is considered a low-cost and low-risk procedure recommended by several guidelines, including NICE, before proceeding to pharmacological or mechanical induction. Despite its widespread use, little evidence is available regarding how women perceive and experience this procedure. In this single-center, prospective observational study, women with low-risk singleton pregnancies between 40+0 and 41+2 weeks of gestation will be recruited at the Oltretermine outpatient clinic of Fondazione Policlinico Universitario Agostino Gemelli, Rome. After providing informed consent, participants who undergo membrane sweeping will be invited to take part in a semi-structured interview within 48-72 hours postpartum during hospital stay. The primary objective is to describe women's lived experiences of membrane sweeping at term. Secondary objectives include describing women's sociodemographic and obstetric characteristics and their overall birth experience. Data will be analyzed thematically to identify recurring concepts and themes. This study is independent, non-funded, and will enroll approximately 12-20 women, until data saturation is reached. All procedures comply with the Declaration of Helsinki, GDPR, and national privacy regulations.

Interventions

None listed

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Women aged \>18 and ≤40 years * Women with singleton pregnancy * Women with cephalic presentation * Women able to read and understand the Italian language * Women with gestational age between 40+0 and 41+2 weeks * Signed informed consent provided by the participant

Exclusion criteria

* Women younger than 18 years or older than 40 years * Women unable to read and understand the Italian language

Design outcomes

Primary

MeasureTime frameDescription
Lived experience of membrane sweepingWithin 48-72 hours after childbirthQualitative description of women's perceptions, feelings, and overall experience related to membrane sweeping at term. Data will be collected through semi-structured interviews and analyzed thematically.

Countries

Italy

Outcome results

None listed

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