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Center for Social Policy
McCormack Graduate School 
University of Massachusetts Boston
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Boston, MA 02125-3393
Phone: (617) 287 5550
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HMIS-Tracking the Homeless: What It Is and What It Means
Author(s):
Cynthia J. Baron

Source(s):
Spare Change News

Date: December 11, 2003

Some homeless people do not want to give information about themselves when they stay at a shelter. Some shelters don't want to spend scarce dollars and precious staff time to collect this data and enter it into a specially programmed computer. But by the fall of 2004, as mandated by a Congressional directive in 2001, all HUD funded homeless service providers in the US must implement HMIS (homeless management information system), an integrated system for collection and transmission of data on the homeless population in order to receive Housing and Urban Development (HUD) funding (through the McKinney-Vento Act).

This means getting at the very least 17 pieces of information according to HUD's draft HMIS Data and Technical standards on the homeless men, women and children participating in HUD funded programs, information that includes such things as gender; race; age and living situation prior to shelter stay. Some sample communities, including Boston, will be required to collect additional information such as special needs, e.g., alcohol problem, mental health problem, drug problem; health coverage and income.

I spoke with Julia Tripp and Nancy Sullivan both of whom work at the University of Massachusetts Boston's (UMB) Center for Social Policy (CSP) at the McCormack Graduate School of Policy Studies. CSP was chosen to set up HMIS for the state of Massachusetts. Julia Tripp, 11 years homeless and a drug addict, has worked for 7 years with the HMIS project, starting long before it became a mandated program, and gives the consumer perspective at all phases of the project. Nancy Sullivan is the CSPTech (the same initials as the Center for Social Policy, but here CSP stands for Connection, Service and Partnership through Technology) Project Manager. She gives the point of view of the project's central focus. The two are sometimes on the same page and sometimes quite divergent in their outlook.

Homeless people using shelters (and other service programs such as an outreach program) are asked to give a staff person at least 17 pieces of information, but usually a good bit more than that. At large shelters, like the Pine Street Inn, there is a feature called "the bed register"-when the homeless person enters the shelter only a few pieces of basic information are collected, then the person is checked into a bed. Later on a shelter staff person will get more detailed information.

Homeless people may not want to give information for HMIS, but Sullivan says that according to CSPTech's Policies and Procedures, homeless consumers have the right not to answer any question, unless entry into a program requires it, but many consumers choose voluntarily to give information. "Nonetheless," says Tripp, "I think there's a lot of feeling in the homeless community that this is an invasive system, that it's not going to help them; it's going to make them known to the powers that be … that the data will be made public and/or be used against them." Sullivan stresses that there are important privacy protections in place to prevent these fears from becoming a reality: No client records are shared with another agency without written client consent and agencies must specify which pieces of information will be shared. Furthermore, agency executive directors must sign an agreement to share information. In fact, most agencies choose not to do this.

Clients do not have to answer any question if they don't want to and can still receive shelter services. Only entry into a service program such as an outreach program, may require clients to give personal information.

Only shelter staff can view identifying information, not UMB staff and not HUD. Agency staff enter identifying information, but it travels over a secure encrypted connection, so that no one can tell who the person is.

All shelters and other agencies using HMIS must have certificates installed on their computers and must have a password and user name. This limits use of ServicePoint, the computer software for UMB's HMIS, to computers that have certificates. Thus, "I can't go home, jump into ServicePoint and start entering [or accessing] data-I can only do it at a computer where a certificate was installed," says Sullivan.

In fact, Tripp was asked to join the HMIS project precisely because she didn't believe in confidentiality and privacy-she felt "they didn't exist." "Would you," she was asked, "join us and bring that perspective to our work." Her first task was to work with providers (shelter representatives and people from other homeless service groups) and some homeless people and look at the privacy protections policies and whether "HMIS questions were being framed appropriately, and if they were the right questions to ask people to find out what their needs were, where they were at, and what income they had," says Tripp. Later, Tripp formed a consumer advisory committee made up of homeless and formerly homeless people involved in giving input to various parts of the HMIS project.

Sullivan says the CSP wants to expand the consumer advisory committee and to go beyond the committee to "have voices of many consumers … involved in the project and helping to shape that project as we move forward. That's our goal. We're not there yet. We want to connect with groups that may already be formed, connect with [homeless] people who want to be part of the project and to figure out ways to make that happen."

Tripp is also on the project's approximately 25 member steering committee, which is made up of consumers, advocates, providers and funders. She is one of the two consumers now part of this committee, and wants to expand the number so more homeless people can participate. She gives the caveat that before they join, homeless people must "come through some process that informs them first so that the questions they can put to the steering committee are informed questions. You need to understand what this damned thing is before you start fighting it. This could be a powerful tool for people that are homeless." One example of homeless people's use of the system is that they would be able to say, "I know you have this [and that] available; these are the things I think I need-am I eligible [according to the information you have on me]?" Tripp points out.

According to the privacy protections, homeless people don't have to answer any question if they don't want to, and they will still receive shelter services. Why, then, would any of them contribute personal information for HMIS. Sullivan says, "Our goal is that if we can build trust, and we can explain what we are doing with the consumer population and they feel more secure about the system, they might be more apt to give information that's accurate and detailed, which would then help us with producing really good quality data."

However, Julia argues cynically, "Although a lot of times homeless people don't realize the connection between data collection and findings, [those who do might well ask] 'How does that make me feel any more comfortable giving up all my information because I know that this shelter that doesn't treat me right is going to get a whole lot of money to keep doing a lousy job?'"

What homeless people may not realize is that UMB's CSP analyzes the data they collect to put out comprehensive reports on the homeless population with the goal of impacting policy, making it more likely, for example, that gaps in the system are clearly recognized and that the system works more effectively to help transition consumers into permanent housing.

Tripp characterizes HMIS data analysis as a tool "that shows a picture, a snapshot, if you will, of who is in the system, what services they're using, and so, what happens to them as they move through the system. With HMIS the whole hope is that we will look at [and ask], "Is the homeless service delivery system being effective-is it moving people out of homelessness, if not, why not?'"

In general, Tripp agrees with Sullivan that trust is the issue about the homeless giving data about themselves. She sees it as depending on a trusting relationship between the homeless person and his/her case manager or other staff person at the shelter: "I think giving your information up means developing a relationship of trust between you [the staff person] and me [the consumer]. You're going to help me … there's a trust between me and the system … those are different levels of trust that have to be learned …" She also notes that giving information may now start at the shelters, but, in fact, to get an apartment or, as Tripp has just done, to get a condominium, you must give up a lot of information about yourself. Sullivan observes that according to HUD's data Data and Technical Standards, consumers may be asked to divulge identifying information such as social security numbers. Tripp also fears "the privilege of anonymity is coming to a close."

Actually, the Congressional mandate for HMIS implementation directed Continuums of Care (CoCs) to give reports from member agencies. CoCs are groups of HUD funded agencies (including some shelters) that meet throughout the year to determine what the needs are of their homeless population and what are the gaps in services for them-they determine services needed to meet these needs and apply for appropriate HUD funding. Since the mandate, HUD has added an HMIS section to their applications for the funds. Massachusetts has 21 CoCs.

At this point CSP gets funding from a few CoCs and from the State. Over the years, state funding has supported CSPTech's work with emergency shelters meaning that shelters have been able to work with CSPTech free of charge. CSPTech is still awaiting notification of its state funding award for this fiscal year. Shelters, however, must purchase a computer and a high speed connection. (HMIS is an unfunded mandate so there are no additional funds available for its implementation and maintenance.) They must also have a staff person who can devote time to data collection and data entry. Although they know they need to implement HMIS, some shelters don't want to take money from supplying services to their homeless populations to support the directive. Some shelters have been collecting data for a number of years already, while others are just starting now because they have to. It's a tough situation for these shelters and they can be very reluctant contributors to data collection. Tripp comments on this dilemma, saying, "Everyone's got to tow the line and a lot of people don't want to do it, but it's a mandate [so] we've got to figure out how to get the best effort out of this tool that's sucking up a lot of money but yet could actually show us the right direction to head in around policy."

UMB's CSP took on the HMIS project because they wanted to analyze this data. "There was a real interest here because the goal was to use data from HMIS to impact public policy. CSP has a long history of doing research on issues affecting low-income people, for instance, food stamps and welfare reform, and having a solid reputation for this work,, they originally got funding from the City of Boston, then some funding by the State. As time went on, they took on other HUD funded CoCs and grew naturally to be the statewide organization for HMIS.

CSP puts out reports for CoCs they have a contract with, reports not widely circulated but rather done specifically for them. However, they also put out comprehensive statewide reports from analysis of their data, which, based on policies developed by the project's steering committee, must represent at least 60 percent of those persons served in a region before being released. Sullivan feels the data is good because it reaches the 60 percent threshold but hopes for even better data in the future. Tripp, reviewing the as yet unreleased statewide report for 2002 on characteristics of homeless individuals sees much room for improvement. The report is not accurate, she says, "because it's not based on every single shelter in the city and not every [homeless person] is giving their information, so it produces a kind of picture-over time, that picture will get clearer." In fact, the data for the statewide report for 2001 is based on information collected from 16 shelters, which represent 62 percent of persons served by the shelter system in that year. Comparisons are made with data collected for 1999 and 2000.

The data for 2001, in the latest report released, are quite interesting. The following are a few of the many findings: 52 percent of homeless individuals in the shelter system are white, 28 percent are African Americans and 14 percent are Latino. For education, many individuals have some high school background, have a high school diploma or their GED, Eighteen percent have some college, and 8 percent have a bachelor's degree. Among the number of possibilities for residence prior to entering the shelter, only 6 percent come from a detox or substance abuse center, only 2 percent come from a jail, prison or detention center, and only 1 percent come from a mental health or other hospital. As for having health insurance, only 61 percent have Medicaid or masshealth and 31 percent have no insurance at all. Of those who have income, fully 41 percent have employment income when they enter the shelter, and the average monthly income from employment is $1,115. Data analyzed and compiled include figures for homeless individuals; for individual homeless men and women; for youth, adults and the elderly, and geographic comparisons between those served in Boston, and those served through the remainder of the State. The complete report can be found on the CSP website: www.mccormack.umb.edu/csp/index.jsp. Soon, you will be able to see their statewide report for 2002. HUD wants data so they know what is happening with their money, but beyond that, having a good picture of the actualities of the homeless situation will hopefully enable policy to be directed more fundamentally toward the abolition of homelessness.
 

 

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