Peer-led Service Delivery Model for Pregnant and Lactating Adolescent Girls and Young Women in Zimbabwe
NCT07546344
Adherence, Medication, Behavior
Shangani, Insiza, Zimbabwe
View Trial DetailsNCT Number: NCT04023799
MTN-045 is a cross-sectional study that will utilize questionnaires, including Discrete-Choice Experiments (DCE) and joint decision tasks, to assess couples' preferences related to dual purpose prevention (DPP) products that could be used to prevent unintended pregnancies and HIV infection. Post-survey explanatory in-depth interviews (IDIs) will be conducted with a subset of participants to explore DPP product-related decisions..
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Notify Me18 year–40 year
All sexes
Observational
Makerere University - Johns Hopkins University (MU-JHU) Research, Kampala, Uganda
MTN-045 is a cross-sectional study that will utilize questionnaires, including DCEs and joint decision tasks, and IDIs to assess heterosexual couples' preferences related to DPP products that could be used to prevent unintended pregnancies and HIV infection. One main goal of the study is to determine heterosexual couples' preferences for a DPP product to inform product delivery and future product design to maximize uptake and willingness to use among sub-Saharan African heterosexual couples. Another main goal of the study is to assess the level of influence of the male partner on a woman's preferences for a DPP product and on her decision-making process regarding product preferences and use.
The MTN-045 study population will consist of approximately 400 heterosexual sub-Saharan African couples of reproductive age who have been in a relationship for ≥ 3 months and are interested in contraception and/or HIV prevention. Women who are currently using contraceptives as well as those not using contraceptives will be eligible. Couples who are living together as well as those not living together will be eligible. All participants will complete survey questionnaires, first separately from their partner, then followed by a joint couples' decision task. Up to 80 participants, i.e., one or both partners from a subset of up to 40 couples, will be selected to complete an IDI.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Each member of the couple must meet all of the following criteria to be eligible for inclusion in the study, and both members of the couple must be willing and eligible for the couple to enroll:
For female partner:
For male partner:
Exclusion criteria
Potential participants who meet the following criteria will be excluded from the study along with their partner:
Time frame: 12-15 months during Q2 2019/Q4 2020
Survey questionnaires
Time frame: 12-15 months during Q2 2019/Q4 2020
Discrete-Choice Experiments (DCE)
Time frame: 12-15 months during Q2 2019/Q4 2020
Survey questionnaires
Time frame: 12-15 months during Q2 2019/Q4 2020
Survey questionnaires
Time frame: 12-15 months during Q2 2019/Q4 2020
Survey questionnaires
Time frame: 12-15 months during Q2 2019/Q4 2020
Discrete-Choice Experiments (DCE)
Time frame: 12-15 months during Q2 2019/Q4 2020
Discrete-Choice Experiments (DCE)
Microbicide Trials Network
Network
Dual Purpose Prevention (DPP) Product Preferences Among Couples
Acronym: CUPID
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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