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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04672304
Other study ID # JUH
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 18, 2020
Est. completion date January 30, 2021

Study information

Verified date December 2023
Source University of Jordan
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We will study with the different variables that affect the intention to use long- acting and permanent contraceptive methods among married women in Jordan through a cross sectional study. Self- administered questionnaire will be distributed to aid in data collection.


Description:

In this cross-sectional study, self-administered pre-made questionnaires. (https://docs.google.com/forms/d/e/1FAIpQLSdjuuQynIxu0AAmIbKHg0-iyZgTW0m5847JaX0OZrnl7v7v1w/v iewform ) will be distributed to married women. (Women of childbearing age). The candidates will be selected according to their age (15-49), marital status (married), and pregnancy status (non-pregnant). The data collected through the questionnaires will then be processed and interpreted in order to understand the variables that affect the use of LACM and permanent contraception methods among Jordanian women.


Recruitment information / eligibility

Status Completed
Enrollment 1365
Est. completion date January 30, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 49 Years
Eligibility Inclusion Criteria: - females used or currently using long-term contraception Exclusion Criteria: - never users of contraception

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Al-Husban University Naser
filling a questionnaire

Locations

Country Name City State
Jordan Jordan University Hospital Amman

Sponsors (1)

Lead Sponsor Collaborator
University of Jordan

Country where clinical trial is conducted

Jordan, 

Outcome

Type Measure Description Time frame Safety issue
Primary The use of LACM and permanent contraception methods measure by a questionnaire 2 months
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