NCT01524419

Brief Summary

  1. 1.Increased women's involvement in decision making at labor process correlates with a positive perception of the labor process.
  2. 2.Increased maternal satisfaction with midwifery and gynecological care at labor correlates with a more positive perception of the labor process.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2012

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 25, 2012

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 2, 2012

Completed
28 days until next milestone

Study Start

First participant enrolled

March 1, 2012

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2012

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2012

Completed
Last Updated

May 3, 2012

Status Verified

January 1, 2012

Enrollment Period

3 months

First QC Date

January 25, 2012

Last Update Submit

May 2, 2012

Conditions

Mother (Person)

Keywords

spontaneous labortermsurgicalmechanicalfetal or maternal complications

Study Arms (1)

women after vaginal birth

Eligibility Criteria

Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

women after vaginal birth at term with no mechanical or surgical intervention and with no maternal or fetal complications

You may qualify if:

  • Vaginal labor
  • At term
  • Hebrew/Arabic speakers

You may not qualify if:

  • Mechanical or surgical intervention
  • Maternal or fetal complications

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Obstetrics and Gynecology, Hillel-Yaffe Medical Center

Hadera, Israel, Israel

Location

Study Officials

  • Merav Amos Chen, BA

    Hillel Yaffe Medical Center

    STUDY DIRECTOR

  • Mordechai Hallak, prof

    Hillel Yaffe Medical Center

    PRINCIPAL INVESTIGATOR

  • Elad Mei-Dan, dr

    Hillel Yaffe Medical Center

    STUDY DIRECTOR

  • Mally ehrenfeld, prof

    University of Tel-Aviv

    STUDY DIRECTOR

  • Tammy Schifter, dr

    University of Tel-Aviv

    STUDY DIRECTOR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 25, 2012

First Posted

February 2, 2012

Study Start

March 1, 2012

Primary Completion

June 1, 2012

Study Completion

August 1, 2012

Last Updated

May 3, 2012

Record last verified: 2012-01

Locations

IL(1)