Medical Monitoring Project (MMP)
- How many people with HIV are receiving medical care for HIV?
- How easy is it to access medical care, prevention, and support services?
- What are the met and unmet needs of people with HIV?
- How is treatment affecting people with HIV?
Why is MMP Important?
Frequently Asked Questions for Providers
What is the Medical Monitoring Project (MMP)?
MMP is a cross-sectional, locally and nationally representative sample survey that assesses the clinical and behavioral characteristics of adults with diagnosed HIV in the United States and Puerto Rico, regardless of HIV care status. Information gathered from MMP can be used to help improve the quality of HIV prevention, care, and treatment services for people with HIV throughout the United States. The project is conducted by state and local health departments in partnership with the Centers for Disease Control and Prevention (CDC).
Which health departments are participating?
See the full list of participating areas.
What should I say if my patient asks me about MMP?
- MMP is a legitimate, long-standing project run by the health department and CDC.
- Information from MMP is used by prevention planning groups, policy leaders, health care providers, and people with HIV to advocate for needed resources and improve the quality of those services.
- Participants receive a token of appreciation (typically a gift card).
Even if your patient is not interested in participating, ask them to contact their local MMP staff. This way, the staff know to stop contacting them.
How were my patients sampled?
Like many other reportable health conditions, all HIV diagnoses are reported to public health departments. MMP samples adults with diagnosed HIV from this list of reported cases. Only sampled persons can participate. Sampled persons are contacted either directly by a participating health department or through their providers to obtain consent for their participation.
Will my patient be compensated?
Your patient will receive a token of appreciation (typically a gift card) for taking part in MMP.
What kind of information is collected?
We collect information on various demographic, clinical, and behavioral characteristics. This includes, but is not limited, to the following information:
- Medical history
- Medical and social services
- Prescribed medications
- Clinic visits
For more detail, see the questionnaire and medical record abstraction forms.
Why do you need to look at my patient’s medical record?
Information from the medical record assists with assessing HIV treatment and quality of care at local and national levels. No identifying information (i.e., provider or client names) is maintained.
How has the information from the survey been used?
MMP data have been used to increase awareness and influence local and national policies on matters that impact people with HIV. At the national level, data have been used to assess adherence to clinical guidelines, inform CDC’s anti-stigma campaign, and inform health care providers of ways to improve care for persons with HIV. Locally, MMP data have been used to inform program planning, policy, and funding for services, including the Ryan White HIV/AIDS program. Findings are routinely published in surveillance reports and medical journals and
presented to community planning groups and at national conferences on topics, such as HIV medication prescription, viral suppression, and health care coverage.
How are the data secured?
MMP staff follow strict protocols to ensure the privacy and confidentiality of your patients’ information. No individual identifiers, including patient or provider names or addresses, are sent to CDC, nor will they be released or used in any reports.
Data from the project will be used to inform HIV prevention community planning groups, Ryan White Treatment Modernization Act (TMA) planning councils and consortia, providers of HIV care, people living with HIV Disease, and others to advocate for reducing the gaps in existing resources. The data from MMP will provide an opportunity for policy decisions, resource allocation, and evaluation of prevention and treatment initiatives at the local and national levels to be based on population-based data.
The Health Insurance Portability and Accountability Act (HIPAA) of 1996 permits health care providers to disclose protected health information to public health authorities for the purpose of preventing or controlling disease; for example, as part of this public health surveillance project. For more information about INMMP and the MMP or other surveillance projects, please contact your state or local health department.
- Contact Infomation
Indiana Department of Health
Office: (317) 233-7647