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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: PACTR
Last refreshed on: 29 May 2023
Main ID:  PACTR201801002909246
Date of registration: 24/12/2017
Prospective Registration: Yes
Primary sponsor: self funded
Public title: The effect of a counseling Intervention on Risk of IPV in Pregnant women in Nigeria
Scientific title: 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: 29/12/2017
Target sample size: 96
Recruitment status: Pending
URL:  https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=2909
Study type:  Interventional
Study design:  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  
Phase:  Not Applicable
Countries of recruitment
Nigeria
Contacts
Name: Tochukwu    Uchendu
Address:  Lamingo 930001 Jos Nigeria
Telephone: +2347032282996
Email: tachukwu@yahoo.com
Affiliation:  Senior Registrar/ JUTH
Name: Tochukwu    Uchendu
Address:  Lamingo 930001 Jos Nigeria
Telephone: +2347032282996
Email: tachukwu@yahoo.com
Affiliation:  Senior Registrar/ JUTH
Key inclusion & exclusion criteria
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
Health Condition(s) or Problem(s) studied

Intimate Partner Violence
Intimate Partner Violence
Intervention(s)
IPV screening and risk assessment
counselling
Primary Outcome(s)
mean IPV risk (measured by Danger assessment score)
Secondary Outcome(s)
demographic characteristics
Prevalence of IPV
Secondary ID(s)
Source(s) of Monetary Support
self funded
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date: 02/11/2016
Contact:
Institutional Health Research Ethical Committee, Jos University Teaching Hospital
Results
Results available:
Date Posted:
Date Completed:
URL:
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