Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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PACTR |
Last refreshed on:
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29 May 2023 |
Main ID: |
PACTR201801002909246 |
Date of registration:
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24/12/2017 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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The effect of a counseling Intervention on Risk of IPV in Pregnant women in Nigeria
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Scientific title:
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The Effect of a clinic based counselling Intervention on Risk reduction of Intimate Partner Violence among Pregnant women attending Antenatal Clinics of Jos UNiversity Teaching Hospital- a Randomized Controlled Trial |
Date of first enrolment:
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29/12/2017 |
Target sample size:
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96 |
Recruitment status: |
Pending |
URL:
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https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=2909 |
Study type:
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Interventional |
Study design:
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Parallel: different groups receive different interventions at same time during study,Randomised,Simple randomization using a randomization table created by a computer software program,Sealed opaque envelopes
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Phase:
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Not Applicable
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Countries of recruitment
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Nigeria
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Contacts
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Name:
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Tochukwu
Uchendu |
Address:
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Lamingo
930001
Jos
Nigeria |
Telephone:
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+2347032282996 |
Email:
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tachukwu@yahoo.com |
Affiliation:
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Senior Registrar/ JUTH |
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Name:
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Tochukwu
Uchendu |
Address:
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Lamingo
930001
Jos
Nigeria |
Telephone:
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+2347032282996 |
Email:
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tachukwu@yahoo.com |
Affiliation:
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Senior Registrar/ JUTH |
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Key inclusion & exclusion criteria
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Inclusion criteria: All clients attending ANC in JUTH within the study period who are at least 18 years of age, with gestational ages 24 weeks or less, calculated from last menstrual period or earliest obstetric Ultrasound scan done, and have given consent to participate in the study.
All pregnant women are included because they are all considered to be at risk of IPV since pregnancy, by itself, is a risk factor for IPV.
Exclusion criteria: 1. ANC attendees who are acutely ill as their need for care will be prioritized and they may not be able to respond to the questions.
2. ANC attendees whose partners have insisted on being present at the interview as that may cause them to withhold or falsify information.
3. ANC attendees who plan to relocate within the 12 week study period as follow up may become difficult when they do so.
4. ANC attendees who do not have intimate partners as that precludes them from suffering from IPV; for example, attendees who do not have intimate partners but got pregnant from rape by a stranger or other persons with whom she is not intimate.
Age minimum:
18 Year(s)
Age maximum:
99 Year(s)
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Intimate Partner Violence
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Intimate Partner Violence
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Intervention(s)
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IPV screening and risk assessment
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counselling
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Primary Outcome(s)
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mean IPV risk (measured by Danger assessment score)
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Secondary Outcome(s)
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demographic characteristics
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Prevalence of IPV
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Source(s) of Monetary Support
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self funded
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Ethics review
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Status: Approved
Approval date: 02/11/2016
Contact:
Institutional Health Research Ethical Committee, Jos University Teaching Hospital
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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