Effect Of Letter Of Invitation Through Mother Support Group Counselling To Enhance Male Involvement In Prevention Of Mother To Child Transmission Of HIV Program In Bale Zone, South East Ethiopia: Quasi Experimental Study
letter of invitation on MI in PMTCT service
Services Research Study
Summary
Study start date: June 22, 2022
Actual date on which the first participant was enrolled.This study aims to enhance male participation in preventing the transmission of HIV from mothers to their children in Bale Zone, South East Ethiopia. Traditionally, male involvement in maternal health, especially in HIV prevention programs, has been low. This lack of involvement can hinder efforts to reduce pediatric HIV infections. The study tests a new approach by sending formal invitation letters through mother support groups to pregnant women attending their first antenatal visit without their partners. This method hopes to encourage male partners to join their partners in future appointments, increasing their participation in HIV counseling and testing. Participants in this study include pregnant women who are visiting antenatal care clinics without their partners. These women will receive a formal invitation letter to give to their partners, encouraging them to attend the next antenatal appointment. The study is conducted in two hospitals, with one group receiving the invitation letters and the other following the usual care procedure. Researchers will collect data through questionnaires and analyze the results to see if the invitation letters increase male attendance and participation in HIV testing. The goal is to find effective methods to boost male involvement in maternal health, ultimately decreasing the rate of mother-to-child HIV transmission.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.400 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 49 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location