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Postpartum Contraception Counseling on the Rate of Unintended Pregnancy

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ClinicalTrials.gov Identifier: NCT02901639
Recruitment Status : Recruiting
First Posted : September 15, 2016
Last Update Posted : June 27, 2018
Sponsor:
Information provided by (Responsible Party):
Ahmed Mohamed Abbas, Assiut University

Brief Summary:
Unwanted pregnancies are not only the major cause of maternal mortality and morbidity but are also a great social and financial burden on societies and countries. According to World-health-organization statistics, there are an estimated 200 million pregnancies around the world each year, and a third of these, 75 million, are unwanted. Unintended pregnancy also is a major health problem in the United States of America. In the 2002 National Survey of Family Growth assessment, 1.22 million, or 31%, were reported as unintended. When abortions were included, unintended pregnancies increased to 2.65 million, or 49% of all pregnancies

Condition or disease Intervention/treatment Phase
Improving Quality of Life Other: counseling Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 300 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Influence of Immediate Postpartum Contraception Counseling on the Rate of Unintended Pregnancy in Primigravida: A Randomized Controlled Study
Actual Study Start Date : September 2016
Estimated Primary Completion Date : August 2018
Estimated Study Completion Date : November 2018

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: counseling group
will receive counseling about contraceptive methods using illustrations through postpartum interview with the study
Other: counseling
No Intervention: NO counseling
will not receive any counseling about contraceptive methods



Primary Outcome Measures :
  1. The difference in the rate of unintended pregnancy in both groups [ Time Frame: 6 months ]


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Ages Eligible for Study:   18 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Age: above 18 years
  2. Primigravida
  3. Women who will accept to participate in

Exclusion Criteria:

  1. Women who are not intended to use contraception
  2. Multiparous
  3. Women who refuse to participate in the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02901639


Locations
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Egypt
Ahmed Abbas Recruiting
Assiut, Cairo, Egypt, 002
Contact: ahmed abbas       bmr90@hotmail.com   
Sponsors and Collaborators
Assiut University

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Responsible Party: Ahmed Mohamed Abbas, Dr, Assiut University
ClinicalTrials.gov Identifier: NCT02901639     History of Changes
Other Study ID Numbers: PPCC
First Posted: September 15, 2016    Key Record Dates
Last Update Posted: June 27, 2018
Last Verified: June 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided