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

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Completed

Conditions

Patient Experience
Labour, Induced
Membrane Stripping
Phenomenology

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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