Effect of the "Adjusted Vocal Expression" Method on the Satisfaction of Parturients About Their Childbirth

NCT ID: NCT02899494

Last Updated: 2019-08-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

251 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-10-31

Study Completion Date

2016-11-07

Brief Summary

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To emit voluntarily sounds mastered during the childbirth is a practice found in certain cultures of country of Africa or Muslim or gypsy traditions. Today, because of the medical coverage and because of the childbirth in a hospital environment, this tradition is not anymore transmitted.

The emission of a sound vibration conjugated to a positive intention managed during the childbirth was experimented with around thirty mothers. In the term of this pilot study, most of the women expressed one felt very positive towards the new method, in particular when they compared it with a previous childbirth where this method was not used.

During these childbirths, the midwives also indicated a shortening of the working time.

The present study aim essentially is to confirm the positive effect of the method on the felt of the childbirth.

Detailed Description

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Conditions

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Pregnancy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Group A

Antenatal classes

Group Type OTHER

Antenatal classes

Intervention Type OTHER

Group B

Physical and psychic preparation

Group Type EXPERIMENTAL

Physical and psychic preparation

Intervention Type OTHER

Interventions

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Antenatal classes

Intervention Type OTHER

Physical and psychic preparation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Women of more than 18 years old
* Primipara
* Patients joining the antenatal classes dispensed by the midwives.
* Patients affiliated to a national insurance scheme or benefiting from such a diet
* Patients having given a written consent form

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hopital Foch

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jean-Marc AYOUBI, PhD

Role: PRINCIPAL_INVESTIGATOR

Hopital Foch

Locations

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Maternité Catherine BARET de Pertuis

Pertuis, , France

Site Status

Hopital Foch

Suresnes, , France

Site Status

Countries

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France

Other Identifiers

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2012-A00716-37

Identifier Type: OTHER

Identifier Source: secondary_id

2012/10

Identifier Type: -

Identifier Source: org_study_id

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