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NCT Number: NCT04023799

Couple User Preferences in Dual Purpose Prevention Products

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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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Makerere University - Johns Hopkins University (MU-JHU) Research, Kampala, Uganda

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About this study

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.

Who can participate

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:

  • Able and willing to provide written informed consent in one of the study languages.
  • Able and willing to complete the required study procedures.
  • Currently in a heterosexual relationship (living together or not) for at least 3 months (by self-report) with the other member of the couple.
  • At time of Enrollment, expressed interest in contraception and/or HIV prevention (by self-report).

For female partner:

  • Between the ages of 18 to 40 years (inclusive) at Enrollment, verified per site standard operating procedures (SOPs).
  • HIV negative (by self-report).

For male partner:

  • Aged 18 years or older at Enrollment, verified per site SOPs.

Exclusion criteria

Potential participants who meet the following criteria will be excluded from the study along with their partner:

  • Has any significant medical condition or other condition that, in the opinion of the Investigator of Record (IoR)/designee, would preclude informed consent, make study participation unsafe (including risk for IPV as a result of study participation), complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.

Treatment and study plan

Primary outcomes

  1. Attributes of a DPP product that influence preferences among heterosexual couples

    Time frame: 12-15 months during Q2 2019/Q4 2020

    Survey questionnaires

  2. Differences in DPP product attribute preferences when comparing individual to couples' choices (e.g., woman's individual preferences vs. preferences indicated through the joint couples decision task)

    Time frame: 12-15 months during Q2 2019/Q4 2020

    Discrete-Choice Experiments (DCE)

Secondary outcomes

  1. Salient relationship-based and decision-making factors that influence DPP product interest and preferences

    Time frame: 12-15 months during Q2 2019/Q4 2020

    Survey questionnaires

  2. Differences in attributes salient to preferences by sociodemographic factors such as age and parity that may reflect lifecourse stage

    Time frame: 12-15 months during Q2 2019/Q4 2020

    Survey questionnaires

Other outcomes

  1. Salient relationship characteristics, norms and communication factors that influenced participants' decision-making process

    Time frame: 12-15 months during Q2 2019/Q4 2020

    Survey questionnaires

  2. Differences in product preferences, when comparing individual to couples' choices, that characterize the male partner's role in females' preferences

    Time frame: 12-15 months during Q2 2019/Q4 2020

    Discrete-Choice Experiments (DCE)

  3. Likelihood of using each DPP product, overall and by subgroup, as estimated through analysis of DCE data

    Time frame: 12-15 months during Q2 2019/Q4 2020

    Discrete-Choice Experiments (DCE)

Sponsors and collaborators

Lead sponsor

Microbicide Trials Network

Network

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • National Institute of Allergy and Infectious Diseases (NIAID)
  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Dual Purpose Prevention (DPP) Product Preferences Among Couples

Acronym: CUPID

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jul 18, 2019
Registry last updated
Oct 13, 2022

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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