Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02657200
Other study ID # EC/2015/0589 AND EC/2015/0590
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2015
Est. completion date September 2016

Study information

Verified date May 2021
Source University Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

KAP-study in Flemish midwives with intramural employment


Description:

The study will be conducted using a self designed questionnaire administered in midwives who are employed within a Flemish hospital in one of the following departments: maternity, maternal intensive care, (intensive) neonatology, reproductive medicine, gynaecology, delivery and prenatal care. The questionnaire assesses the knowledge, attitude and practices of the midwives regarding spontaneous abortion.


Recruitment information / eligibility

Status Completed
Enrollment 647
Est. completion date September 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: - midwives who are employed within a Flemish hospital in one of the following departments: maternity, maternal intensive care, (intensive) neonatology, reproductive medicine, gynaecology, delivery and prenatal care Exclusion Criteria: - all others

Study Design


Related Conditions & MeSH terms


Intervention

Other:
survey
questionnaire assessing the knowlegde, attitude and practices regarding spontaneous abortion

Locations

Country Name City State
Belgium AZ Sint-Jan Brugge West-Vlaanderen

Sponsors (2)

Lead Sponsor Collaborator
VakgroepVolksgezondheidEnEerstelijnszorg Odisee

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary knowledge, attitude and practices regarding spontaneous abortion Based on previous published KAP-studies, a questionnaire was designed and tested using a single Delphi procedure with experts and lay persons. The knowledge items include questions on the definition, treatment, side effects, risk factors and legal aspects of spontaneous abortion. The attitude items include questions about the attitude of midwives when confronted with women with spontaneous abortion, and how they perceive the role of midwives in delivering various aspects of care to women with spontaneous abortion. The practices items include questions about the extent to which midwives are confronted with women with spontaneous abortion, and about the characteristics of these cases. In addition, midwives are asked about the availability of training and protocols to deliver care to women with spontaneous abortion. Each item will be treated as a categorical variable. A sum score will be calculated counting the correct answers of the knowledge questions. 6 months
See also
  Status Clinical Trial Phase
Recruiting NCT03332706 - the Association Between Blood's and Urinary Heavy Metal Level in Pregnant Women and the Spontaneous Abortion N/A
Recruiting NCT04003064 - Heavy Metals' Influence on Early Pregnancy Through Oxidative Stress
Completed NCT01857310 - Folic Acid and Zinc Supplementation Trial (FAZST) N/A
Completed NCT00467363 - The Effects of Aspirin in Gestation and Reproduction N/A
Recruiting NCT04456660 - Comprehensive Assessment of Risks for Miscarriage.
Completed NCT00878098 - Study of DDT and Loss of Clinically-Recognized Pregnancies in South Africa
Recruiting NCT04705324 - Dilation and Curettage Versus Operative Hysteroscopy for Missed Abortion N/A
Completed NCT02012491 - Comparative Effectiveness of Pregnancy Failure Management Regimens Phase 3
Recruiting NCT05492708 - The Heartland Study
Completed NCT04017754 - Low Plasma Mannose Binding Lectin (p-MBL) Level is a Risk Factor for Recurrent Pregnancy Loss (RPL)
Active, not recruiting NCT04156126 - Measuring Immune Tolerance to Predict Miscarriage or Failed Embryo Transfer
Completed NCT02725710 - Gabapentin as an Adjunct to Perioperative Pain Management Regimens for Uterine Aspiration Phase 2
Recruiting NCT04182503 - Environmental Factors and Embryonic Development Project