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Completed

NCT Number: NCT02352961

An Implementation Science Study Investigating Profiles of Men Interested in MMC

There are both supply and demand gaps in our understanding of how best to implement MMC services. In terms of supply of MMC services, there is a need to better understand what the best way is of efficiently accessing mature men(25-49 years old) . The investigators also want to understand the type of service delivery approach and environment that would make mature men(25-49 years old) feel more comfortable when attending an MMC clinic. Demand of MMC requires identifying messaging that works to address mature men's (25-49 years old) issues so that they might be willing to undergo MMC. To further advance HIV prevention and advocacy of male circumcision the investigators also need to consider the perspectives of women on what approach MMC messaging should take. A combination of male and female viewpoints could inform MMC outreach messaging where IEC materials are tailored to address the barriers to MMC. Identifying the specific barriers to MMC among males and including the perspectives

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The Aurum Institute

Gauteng, 1632, South Africa

About this study

Part I (Formative Period) Given these issues, in addition to establishing a baseline estimate of the ages and risk behaviours of males currently undergoing MMC at the Aurum clinic over a six month period, we include a qualitative research component. We conducted research in 2014 to establish a baseline estimate of the ages and risk behaviours of males undergoing MMC at the Aurum clinic over a six month period. The baseline estimate (Ethics reference number M130711) will be referred to as the formative Part I. The formative Part I includes a quantitative and qualitative research component. The qualitative component will include both genders and be used to develop MMC recruitment messaging tailored to mature men(25-49 years old) . Men will provide their opinion on circumcision and on what type of marketing message they feel will encourage mature men (25-49 years old) to be circumcised. Women will also provide their perspectives on male circumcision and what messaging could be used to encourage their partners or male family members to be circumcised. During this study, we explored if women have a role in promoting male circumcision to their partners, family and the community. These qualitative findings will be used to develop interventions to increase the ratio of men (25-49 years old) mature, or at least of higher risk men, undergoing MMC at the clinic. These interventions and the outcomes related to them will be presented as an amendment to this protocol after the baseline and qualitative data are collected and analysed.

Part II (Intervention Period) Findings from the formative period will be used to develop interventions to increase the ratio of men (25-49 years)mature, or at least of higher risk men, undergoing MMC at the clinic. During this proposed intervention period we would like to evaluate the effectiveness of those interventions and the outcomes related to them. These proposed interventions will directly address the barriers to MMC that challenge uptake of MMC among mature men (25-49 years). Additionally, epidemiologic research will be conducted among men attending our MMC clinic to evaluate whether mature men (25-49 years) exhibit, as is presumed, higher risk profiles for HIV. We will also explore the cost-effectiveness of this strategy.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for Cross Sectional Component Inclusion Criteria:

All males who meet the following criteria will be eligible for inclusion:

  • Are aged 18 years or older (no upper age limit)
  • Have never been completely medically circumcised (as opposed to partial circumcision)
  • Willing and able to give their written informed consent so that the information collected during the clinic visit can be analysed for research purposes.

Inclusion criteria

Qualitative Component for males

All males who meet the following criteria will be eligible for inclusion:

  • Present at Aurum's male circumcision clinic during the cross sectional component or men who indicate no interest in medical male circumcision
  • Are between the ages of 25 and 49 inclusive
  • Are not circumcised at the time of the interview as assessed through visual examination
  • Is willing and able to provide written informed consent.
  • Willing for the qualitative session to be tape recorded

Inclusion criteria

for Qualitative Component for females Women who meet the following criteria will be eligible for inclusion

  • Are 18 and above (no upper age limit)
  • Has a partner who is participating in the cross sectional component, is not in a relationship but lives in the vicinity of Ekurhuleni North district or is part of a women's organization within the community where the clinic is located
  • Is willing and able to provide written informed consent
  • Willing for the qualitative session to be tape recorded

Inclusion criteria

Part II (Intervention Period) Inclusion Criteria for the "Exclusive Intervention Strategy" Men who meet the following criteria will be eligible for inclusion in the intervention period

  • Are between the ages 25 and 49 years inclusive
  • Has never been medically circumcised
  • Is willing and able to provide written informed consent

Inclusion criteria

for the "Active Follow-up Intervention" Men who meet the following criteria will be eligible for inclusion

  • Are between the ages 25 and 49 years inclusive
  • Has never been medically circumcised
  • Is willing and able to provide written informed consent
  • Has contra-indication/s to MMC on the day of presentation for MMC
  • Is willing to provide contact information for retention

Exclusion criteria

for all Aims:

  • Men who are unable to communicate sufficiently (in English or local languages) to complete medical forms and/or research questionnaires for the cross sectional component.
  • Men and women who do not in the opinion of staff obtaining consent have the capacity to provide written informed consent will be excluded from the research.

Treatment and study plan

Exclusive Intervention Strategy

Other

The "Exclusive Intervention Strategy" aimed at men aged 25 - 49 years and "Active Follow-up strategy"

Primary outcomes

  1. Current proportion of mature men (25-49 years) presenting for and undergoing MMC

    Time frame: 6 months

    To describe the current proportion of mature men (25-49 years) presenting for and undergoing MMC compared to all men (18 and above) during a 6 month period when routine service delivery and outreach messaging will be employed at one Aurum site.

  2. Particular barriers to MMC among men (25-49 years)

    Time frame: 6 months

    To describe the particular barriers to MMC among men (25-49 years) regardless of circumcision status, develop tailored messaging and outreach materials promoting MMC to mature men.

  3. Barriers to MMC and using the perspective of women

    Time frame: 6 months

    To investigate the particular barriers to MMC and using the perspective of women develop tailored messaging and outreach materials promoting MMC to mature men.

  4. Effectiveness of offering an "Exclusive Intervention Strategy"

    Time frame: 6 months

    Evaluate the effectiveness of offering an "Exclusive Intervention Strategy" comprised of customized services to mature (25-49 years) men. To achieve this aim we will compare the proportion of mature men (25-49 years) presenting for MMC during the formative and intervention periods.

Secondary outcomes

  1. Risk behaviours

    Time frame: 6 months

    Identify risk behaviours (e.g. multiple partners; inconsistent condom use and STI symptoms) of men currently presenting at the Aurum MMC clinic.

  2. Compare risk behaviours to national prevalence

    Time frame: 6 months

    Compare risk behaviours of men presenting for MMC with that of national prevalence estimates of risk behaviour.

  3. Risk profile, age and source of recruitment

    Time frame: 6 months

    Describe the risk profile, age and sources of recruitment of men presenting at the clinic. To achieve this aim we will examine each of these factors over time.

  4. Factors associated with the intervention

    Time frame: 6 months

    Identify whether the intervention is associated with HIV risk behaviours (for example multiple partners), having adjusted for age. This is to identify if the intervention has resulted in men attending for MMC with a different risk profile over and above any anticipated age differences.

  5. Socio-demographic factors

    Time frame: 6 months

    Identify socio-demographic factors associated with HIV risk behaviours, among mature men (25-49 years).

  6. Effectiveness of active follow-up

    Time frame: 6 months

    Evaluate the effectiveness of an active follow-up system on completion of MMC among mature men (25-49 years) who present for MMC but who are initially referred for care due to contra-indication to MMC

  7. Cost effectiveness

    Time frame: 6 months

    To determine the cost-effectiveness of this intervention among mature men (25-49 years).

Sponsors and collaborators

Lead sponsor

The Aurum Institute NPC

Other

Collaborators

  • Centers for Disease Control and Prevention

Registry information

Official study title

An Implementation Science Study Investigating Profiles of Men Interested in Medical Male Circumcision (MMC), Barriers and Methods to Increase the Uptake of MMC Among Older Men in South Africa

Acronym: Imbizo

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Feb 2, 2015
Registry last updated
Jan 28, 2016

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.