Mental HealthSRCNCT03616990
Supportive Release Center Study
A study testing TASC Service Linkages - Discharge Area Only, SRC Overnight Stay and TASC Services Linkages - SRC Onsite in people with Mental Health and Mental Health Services, run by University of Chicago at 1 site in United States.
Trial summary
The Supportive Release Center (SRC) is a collaboration between the University of Chicago Urban Health Lab, Treatment Alternatives for Safe Communities, Heartland Alliance Health, and the Cook County Sheriff's office. Read more about this study
- Who is it for?
- Ages 18 years and older, men only
- Conditions the study is for
- Mental Health, Mental Health Services, Substance Use
- What is being tested?
- TASC Service Linkages - Discharge Area Only, SRC Overnight Stay and TASC Services Linkages - SRC Onsite
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 15,195 participants
- Where
- 1 siteUnited States
- Study dates
- 6 Nov 2017to 31 Dec 2025
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Men only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male adult being discharged from Cook County Jail
- Individuals indicating a need for services
- Individuals interested in receiving services
Who cannot join
- Individuals who are not leaving Cook County Jail
- Female individuals
- Individuals without acute social needs
- Individuals below 18 years of age
Trial locations and contacts
1 site in 1 country.
United States1 site
Cook County Department of Corrections & SRC
Chicago, Illinois, 60608
About this study
The Supportive Release Center (SRC) is a collaboration between the University of Chicago Urban Health Lab, Treatment Alternatives for Safe Communities, Heartland Alliance Health, and the Cook County Sheriff's office. The aim of the SRC is to identify individuals with mental illnesses, substance use disorders, and other vulnerabilities as they are released from the Cook County Jail (CCJ), provide an improved environment to assess needs of these individuals, and facilitate effective linkages with social services following release, including medical care and substance use or mental health treatment. The SRC improves the current standard of care offered at the CCJ by introducing mechanisms to facilitate engagement with post-release services and address individuals' immediate acute needs. The primary objective of this randomized controlled trial is to evaluate the impact of assignment to the SRC on the number of arrests within one year of study enrollment among eligible men being released from the Cook County Jail. Researchers hypothesize that the SRC is more effective than usual care at facilitating and ensuring receipt of transition services and care, and that receipt of this treatment will decrease the number of arrests within one year of study enrollment.
Read the detailed description
The University of Chicago Health Lab is working with service providers - Treatment Alternatives for Safe Communities (TASC) and Heartland Alliance Health (HAH) - and the Cook County Sheriff's Office (CCSO), to implement a randomized controlled trial of a Supportive Release Center (SRC) compared to usual care for persons leaving the Cook County Jail (CCJ) with mental health, substance use disorder, or acute health needs. The primary aim of this randomized controlled trial is to evaluate the impact of assignment to the SRC, compared with not being offered a placement at the SRC (and consequent usual care), on the number of arrests within one year of study enrollment among eligible men being discharged from CCJ.
The recruitment strategy for the SRC intervention is integrated into the jail discharge process. Individuals are discharged from the CCJ in groups, such that they may wait several hours before being discharged. After being escorted to the discharge area, detained individuals are consented to participate in the SRC study and asked to take a survey designed to identify needs, vulnerabilities, and interest in receiving services. During consent, individuals are informed that their CCJ Booking ID will be used to acquire data from the CCSO, Chicago Police Department, Illinois Criminal Justice Information Authority, and Illinois State Police to determine their history of arrest, time spent in jail, and instances of re-arrest following study enrollment. In conjunction with demographic information linked from CCSO, this ID can be used to track healthcare and social service utilization via databases administered by Cook County Health and Hospital System (CCHHS), the Centers for Medicare and Medicaid Services, the Illinois Department of Healthcare and Family Services, the Illinois Department of Public Health, the Chicago Fire Department, and collaborating service-providers (TASC and HAH).
Eligibility for the SRC intervention requires survey responses indicating both (1) vulnerability, suggesting potential need for the SRC, and (2) interest in attending the SRC. Vulnerability that suggests potential need for the SRC is ascertained by four independent criteria: a response of "more than half the days" or "nearly every day" to questions (1) and (2) from either the PHQ-9 depression or Generalized Anxiety Disorder (GAD)-7 modules, which refer to problems experienced "over the past 2 weeks" (PHQ: 1. "little interest or pleasure doing things", 2. "feeling down, depressed, and hopeless"; GAD: 1. "feeling nervous, anxious, or on edge", 2. "not being able to stop or control worrying"); two or more previous instances of incarceration over the past 12 months; history of substance use over the previous 12 months, indicated by weekly or more than weekly consumption of i) more than five alcoholic drinks per day, or ii) prescription drugs for non-medical reasons, or iii) illegal drugs; or affirmative response to questions asking about previous diagnosis by a health professional for a mental health condition, existence of urgent needs for healthcare over the three weeks following discharge, or concern about personal safety during discharge from the jail. Two questions gauge respondent interest in attending the SRC: interest in having (i) a safe place to stay upon discharge or (ii) a place to go to receive connections with social services upon discharge. An individual who responds affirmatively to both "interest" questions is automatically eligible for the SRC; to be eligible with an affirmative response to only one "interest" question, the respondent must have at least one indicator of vulnerability. Individuals who do not respond affirmatively to either question about interest are not eligible for the SRC.
Detainees who are eligible and interested in services are then randomized to treatment and control groups. Individuals who are randomized to treatment have individual meetings with TASC social workers in a private office close to the discharge area, where the SRC is explained and offered. TASC provides opportunities to interview and receive service-linkages in the CCJ office for all randomized individuals. In addition to individuals randomized to control, those randomized to treatment who choose not to visit the off-site SRC facility are offered linkages during their private interview with TASC.
The SRC is located on the CCJ campus, one half mile from the point of CCJ discharge. Participants accepting the SRC treatment are transported from the CCJ exit to the facility in TASC vehicles. The facility has the capacity to provide an overnight stay, meal, and shower to twelve individuals per night and provides a private environment where TASC case-workers can meet with discharged individuals. This environment provides TASC staff an opportunity to conduct a more intensive needs-screening to identify appropriate service-linkages, including connection with organizations providing substance use treatment and mental health services. An advanced practice nurse is available at the SRC to address immediate medical needs and ensure continued access to necessary prescription medications. On pre-specified days HAH recruits from the SRC to populate a non-SRC study; individuals recruited from the SRC and individuals randomized to SRC control on days HAH is recruiting are excluded from the SRC study.
Intention-to-treat (ITT) and treatment-on-treated (TOT) analyses will be conducted for specified outcomes. In addition to an ITT group indicator, all models include covariates for demographic information (age, race, Hispanic/Latino indicator) acquired from the CCSO, an indicator variable for whether the individual could qualify for SRC treatment based on that measure ("qualified" (1) vs. "not qualified" or "no response (0)), and an indicator for whether that measure was missing ("no response" (1) vs. "not qualified"or "qualified" (0)) (i.e. PHQ/depression score, GAD anxiety score, previous mental health diagnosis, alcohol use, prescription drug use, illegal drug use, acute health needs, or concern for personal safety). Age (18-24, 25-35, 36-45, 46-55, over 55), race ("black", "white", "other", "unknown"), and ethnicity ("Hispanic/Latino", "not Hispanic/Latino", "unknown") are coded as categorical variables. All models will include an interaction term between age and ITT status. Arrest and hospitalization outcomes will be measured using data from the Illinois State Police and Illinois Department of Public Health acquired via probabilistic matching on demographic identifiers. As a robustness check for count outcomes, researchers will evaluate sensitivity of results to the inclusion of an offset representing the number of days individuals an individual is vulnerable to the outcome. Unexposed time (invulnerable to re-arrest or emergency department visit) is defined as time spent incarcerated or hospitalized.
- Conditions
- Mental Health, Mental Health Services, Substance Use, Continuity of Patient Care, Recidivism
- Being tested
- TASC Service Linkages - Discharge Area Only, SRC Overnight Stay, TASC Services Linkages - SRC Onsite, APN Appointment
- Keywords
- Recidivism, Substance use, Jail, Mental health, Continuity of care, Chicago, Needs Assessment
- Medical subject headings
- Psychological Well-Being, Substance-Related Disorders, Recidivism
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
TASC Service Linkages - Discharge Area OnlyBehavioural
Individuals will meet with TASC Care Coordinators in the discharge area of the Cook County Jail. Individuals will be screened for housing, health and behavioral health needs and then linked to appropriate community-based services.
SRC Overnight StayBehavioural
Individuals receiving SRC services will have the option to stay at the SRC overnight. At the SRC, individuals will be able to rest, have a meal, receive a change of clothes, and take a shower in a therapeutic, non-coercive environment.
TASC Services Linkages - SRC OnsiteBehavioural
While at the SRC, individuals will meet with TASC Care Coordinators. Individuals will be screened for housing, health and behavioral health needs and then linked to appropriate community-based services.
APN AppointmentBehavioural
Individuals at the SRC will be able to meet with an Advanced Practice Nurse. As part of that visit, the APN will be able to prescribe medications or reroute prescriptions previously administered by the Cook County Jail's hospital, Cermak, to a participant's desired location as needed.
| Study group | Role | What they receive |
|---|---|---|
| Usual Care (Control) | Active comparator | Usual care. These individuals will receive linkages to community-based services only. These linkages will be made while in the Discharge Area of the Cook County Jail. Individuals randomized on days Heartland Alliance Health recruits at SRC for non-SRC study are excluded from population.
Receives: TASC Service Linkages - Discharge Area Only Receives: Behavioral: TASC Service Linkages - Discharge Area Only |
| Supportive Release Center (Treatment) | Experimental | These individuals will receive SRC services: an overnight stay at the SRC, linkages to community-based services made at the SRC or in the discharge area of the CCJ if they choose not to visit the SRC facility, and access to an Advanced Practice Nurse. Individuals randomized on days Heartland Alliance Health recruits at SRC for non-SRC study are excluded from population.
Receives: TASC Service Linkages - Discharge Area Only -OR- SRC Overnight Stay, TASC Services Linkages - SRC Onsite, APN Appointment Receives: Behavioral: TASC Service Linkages - Discharge Area Only; Behavioral: SRC Overnight Stay; Behavioral: TASC Services Linkages - SRC Onsite; Behavioral: APN Appointment |
What is being measured
The primary outcome is the main question the study is designed to answer.
Re-arrest count
Number of re-arrests within 365 days of study enrollment, measured at the individual level using Illinois State Police arrest records. Follow-up will begin the day an individual is first randomized (index randomization) and ITT group membership will be based upon index treatment assignment. Given expected dispersion and excess zeroes in the final dataset, the ITT treatment effect will be modeled using zero-inflated negative binomial regression. ITT analyses will be supplemented by a TOT analysis treating randomization as an instrument. Covariates for this outcome will include ordinal measures of arrest history (0, 1-2, 3-5, 6-10, and >10 arrests) and days incarcerated (0, 1-7, 8-14, 15-30, and >30 days) during the 365 days prior to index randomization.
Measured: 365 days
Secondary outcomes (4)
Emergency department (ED) visits
Number of emergency department visits within 365 days of study enrollment, measured at the individual level using hospitalization records from Illinois Department of Public Health. Follow-up will begin the day an individual is first randomized (index randomization) and ITT group membership will be based upon index treatment assignment. Given expected dispersion and excess zeroes in the final dataset, the ITT treatment effect will be modeled using zero-inflated negative binomial regression. ITT analyses will be supplemented by a TOT analysis treating randomization as an instrument. Covariates for this outcome will include ordinal measures of ED utilization (0, 1-2, 3-5, 6-10, and >10 visits) and days hospitalized (0, 1-7, 8-14, 15-30, and >30 days) during the 365 days prior to index randomization. Emergency department visits that occur during periods of incarceration will be included in the count outcome.
Measured: 365 days
Days until re-arrest
Days until first re-arrest, measured at the individual level using Illinois State Police arrest records. Follow-up will begin the day an individual is first randomized (index randomization) and last for 365 days, after which all individuals not re-arrested will be treated as censored. The hazard ratio associated with treatment assignment (ITT) will be estimated via Cox proportional hazard model. ITT analyses will be supplemented by a TOT analysis treating randomization as an instrument. Model covariates are identical to those included in the primary outcome analysis (count, re-arrests).
Measured: 365 days
Re-arrest count, unique randomizations
Number of re-arrests within 365 days of study enrollment, measured at the randomization level using Illinois State Police arrest records. Follow-up will begin the day a randomization occurs and ITT group membership will be based upon randomization status. Given expected dispersion and excess zeroes in the final dataset, the ITT treatment effect will be modeled using zero-inflated negative binomial regression. To account for correlation between randomizations of the same individual, researchers will employ a 2-level model with random effects at level 2 (individuals). ITT analyses will be supplemented by a TOT analysis treating randomization as an instrument. Model covariates are identical to those included in the primary outcome analysis (count, re-arrests).
Measured: 365 days
Engagement with homelessness services
Existence of formal contact within 30 days of study enrollment, measured at the individual level using utilization records from the All Chicago Homeless Management Information System (HMIS). Follow-up will begin the day an individual is first randomized upon discharge from jail (index randomization) and ITT group membership will be based upon index treatment assignment. The ITT treatment effect will be modeled using a simple logistic model, regressing engagement status on treatment status. We will conduct secondary analysis including covariates for age, race, and offense history.
Measured: 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Aug 2018
- Study start6 Nov 2017
- Primary completion31 Mar 2021
- Study completion31 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Mental HealthStudies of the same condition, open and under way.
- More trials run by University of ChicagoThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Individually-randomized, two-group parallel study
- Masking
- None (open label)
- Enrolment
- 15,195 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Chicago
- Sponsor type
- University, hospital or other
- Collaborators
- Treatment Alternatives for Safe Communities Inc, Heartland Health Research Alliance, Sheriff's Office of Cook County, Illinois, Robert R McCormick Foundation, Pritzker Family Foundation, Laura and John Arnold Foundation, Center for the Advancement of Critical Time Intervention
- Responsible party
- Sponsor
- Investigators
- David Meltzer, MD, PhD, Principal investigator, University of ChicagoHarold Pollack, PhD, Principal investigator, University of Chicago
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03616990
- Sponsor's protocol ID
- IRB16-0536
- Acronym
- SRC
- Status last verified
- Apr 2025
- First submitted
- 30 Jul 2018
- Last updated
- 11 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Supportive Release Center Study
- ClinicalTrials.gov ID
- NCT03616990
- Acronym / sponsor ID
- SRC / IRB16-0536
- Conditions
- Mental Health, Mental Health Services, Substance Use, Continuity of Patient Care, Recidivism
- Keywords
- Recidivism, Substance use, Jail, Mental health, Continuity of care, Chicago, Needs Assessment
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 15,195 participants (actual)
- Lead sponsor
- University of ChicagoUniversity, hospital or other
- Collaborators
- Treatment Alternatives for Safe Communities Inc, Heartland Health Research Alliance, Sheriff's Office of Cook County, Illinois, Robert R McCormick Foundation, Pritzker Family Foundation, Laura and John Arnold Foundation, Center for the Advancement of Critical Time Intervention
- Study start
- 6 Nov 2017 (actual)
- Primary completion
- 31 Mar 2021 (actual)
- Study completion
- 31 Dec 2025 (estimated)
- First posted
- 6 Aug 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The Supportive Release Center (SRC) is a collaboration between the University of Chicago Urban Health Lab, Treatment Alternatives for Safe Communities, Heartland Alliance Health, and the Cook County Sheriff's office. The aim of the SRC is to identify individuals with mental illnesses, substance use disorders, and other vulnerabilities as they are released from the Cook County Jail (CCJ), provide an improved environment to assess needs of these individuals, and facilitate effective linkages with social services following release, including medical care and substance use or mental health treatment. The SRC improves the current standard of care offered at the CCJ by introducing mechanisms to facilitate engagement with post-release services and address individuals' immediate acute needs. The primary objective of this randomized controlled trial is to evaluate the impact of assignment to the SRC on the number of arrests within one year of study enrollment among eligible men being released from the Cook County Jail. Researchers hypothesize that the SRC is more effective than usual care at facilitating and ensuring receipt of transition services and care, and that receipt of this treatment will decrease the number of arrests within one year of study enrollment.
Detailed description
The University of Chicago Health Lab is working with service providers - Treatment Alternatives for Safe Communities (TASC) and Heartland Alliance Health (HAH) - and the Cook County Sheriff's Office (CCSO), to implement a randomized controlled trial of a Supportive Release Center (SRC) compared to usual care for persons leaving the Cook County Jail (CCJ) with mental health, substance use disorder, or acute health needs. The primary aim of this randomized controlled trial is to evaluate the impact of assignment to the SRC, compared with not being offered a placement at the SRC (and consequent usual care), on the number of arrests within one year of study enrollment among eligible men being discharged from CCJ.
The recruitment strategy for the SRC intervention is integrated into the jail discharge process. Individuals are discharged from the CCJ in groups, such that they may wait several hours before being discharged. After being escorted to the discharge area, detained individuals are consented to participate in the SRC study and asked to take a survey designed to identify needs, vulnerabilities, and interest in receiving services. During consent, individuals are informed that their CCJ Booking ID will be used to acquire data from the CCSO, Chicago Police Department, Illinois Criminal Justice Information Authority, and Illinois State Police to determine their history of arrest, time spent in jail, and instances of re-arrest following study enrollment. In conjunction with demographic information linked from CCSO, this ID can be used to track healthcare and social service utilization via databases administered by Cook County Health and Hospital System (CCHHS), the Centers for Medicare and Medicaid Services, the Illinois Department of Healthcare and Family Services, the Illinois Department of Public Health, the Chicago Fire Department, and collaborating service-providers (TASC and HAH).
Eligibility for the SRC intervention requires survey responses indicating both (1) vulnerability, suggesting potential need for the SRC, and (2) interest in attending the SRC. Vulnerability that suggests potential need for the SRC is ascertained by four independent criteria: a response of "more than half the days" or "nearly every day" to questions (1) and (2) from either the PHQ-9 depression or Generalized Anxiety Disorder (GAD)-7 modules, which refer to problems experienced "over the past 2 weeks" (PHQ: 1. "little interest or pleasure doing things", 2. "feeling down, depressed, and hopeless"; GAD: 1. "feeling nervous, anxious, or on edge", 2. "not being able to stop or control worrying"); two or more previous instances of incarceration over the past 12 months; history of substance use over the previous 12 months, indicated by weekly or more than weekly consumption of i) more than five alcoholic drinks per day, or ii) prescription drugs for non-medical reasons, or iii) illegal drugs; or affirmative response to questions asking about previous diagnosis by a health professional for a mental health condition, existence of urgent needs for healthcare over the three weeks following discharge, or concern about personal safety during discharge from the jail. Two questions gauge respondent interest in attending the SRC: interest in having (i) a safe place to stay upon discharge or (ii) a place to go to receive connections with social services upon discharge. An individual who responds affirmatively to both "interest" questions is automatically eligible for the SRC; to be eligible with an affirmative response to only one "interest" question, the respondent must have at least one indicator of vulnerability. Individuals who do not respond affirmatively to either question about interest are not eligible for the SRC.
Detainees who are eligible and interested in services are then randomized to treatment and control groups. Individuals who are randomized to treatment have individual meetings with TASC social workers in a private office close to the discharge area, where the SRC is explained and offered. TASC provides opportunities to interview and receive service-linkages in the CCJ office for all randomized individuals. In addition to individuals randomized to control, those randomized to treatment who choose not to visit the off-site SRC facility are offered linkages during their private interview with TASC.
The SRC is located on the CCJ campus, one half mile from the point of CCJ discharge. Participants accepting the SRC treatment are transported from the CCJ exit to the facility in TASC vehicles. The facility has the capacity to provide an overnight stay, meal, and shower to twelve individuals per night and provides a private environment where TASC case-workers can meet with discharged individuals. This environment provides TASC staff an opportunity to conduct a more intensive needs-screening to identify appropriate service-linkages, including connection with organizations providing substance use treatment and mental health services. An advanced practice nurse is available at the SRC to address immediate medical needs and ensure continued access to necessary prescription medications. On pre-specified days HAH recruits from the SRC to populate a non-SRC study; individuals recruited from the SRC and individuals randomized to SRC control on days HAH is recruiting are excluded from the SRC study.
Intention-to-treat (ITT) and treatment-on-treated (TOT) analyses will be conducted for specified outcomes. In addition to an ITT group indicator, all models include covariates for demographic information (age, race, Hispanic/Latino indicator) acquired from the CCSO, an indicator variable for whether the individual could qualify for SRC treatment based on that measure ("qualified" (1) vs. "not qualified" or "no response (0)), and an indicator for whether that measure was missing ("no response" (1) vs. "not qualified"or "qualified" (0)) (i.e. PHQ/depression score, GAD anxiety score, previous mental health diagnosis, alcohol use, prescription drug use, illegal drug use, acute health needs, or concern for personal safety). Age (18-24, 25-35, 36-45, 46-55, over 55), race ("black", "white", "other", "unknown"), and ethnicity ("Hispanic/Latino", "not Hispanic/Latino", "unknown") are coded as categorical variables. All models will include an interaction term between age and ITT status. Arrest and hospitalization outcomes will be measured using data from the Illinois State Police and Illinois Department of Public Health acquired via probabilistic matching on demographic identifiers. As a robustness check for count outcomes, researchers will evaluate sensitivity of results to the inclusion of an offset representing the number of days individuals an individual is vulnerable to the outcome. Unexposed time (invulnerable to re-arrest or emergency department visit) is defined as time spent incarcerated or hospitalized.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Individually-randomized, two-group parallel study
| Arm | Type | Receives |
|---|---|---|
| Usual Care (Control) | Active comparator | Behavioral: TASC Service Linkages - Discharge Area OnlyUsual care. These individuals will receive linkages to community-based services only. These linkages will be made while in the Discharge Area of the Cook County Jail. Individuals randomized on days Heartland Alliance Health recruits at SRC for non-SRC study are excluded from population. Receives: TASC Service Linkages - Discharge Area Only |
| Supportive Release Center (Treatment) | Experimental | Behavioral: TASC Service Linkages - Discharge Area Only, Behavioral: SRC Overnight Stay, Behavioral: TASC Services Linkages - SRC Onsite, Behavioral: APN AppointmentThese individuals will receive SRC services: an overnight stay at the SRC, linkages to community-based services made at the SRC or in the discharge area of the CCJ if they choose not to visit the SRC facility, and access to an Advanced Practice Nurse. Individuals randomized on days Heartland Alliance Health recruits at SRC for non-SRC study are excluded from population. Receives: TASC Service Linkages - Discharge Area Only -OR- SRC Overnight Stay, TASC Services Linkages - SRC Onsite, APN Appointment |
Who may qualify
- Ages
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Male adult being discharged from Cook County Jail
- Individuals indicating a need for services
- Individuals interested in receiving services
Key exclusion criteria (4 listed)
- Individuals who are not leaving Cook County Jail
- Female individuals
- Individuals without acute social needs
- Individuals below 18 years of age
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| TASC Service Linkages - Discharge Area OnlyIndividuals will meet with TASC Care Coordinators in the discharge area of the Cook County Jail. Individuals will be screened for housing, health and behavioral health needs and then linked to appropriate community-based services. | Behavioural | Supportive Release Center (Treatment), Usual Care (Control) |
| SRC Overnight StayIndividuals receiving SRC services will have the option to stay at the SRC overnight. At the SRC, individuals will be able to rest, have a meal, receive a change of clothes, and take a shower in a therapeutic, non-coercive environment. | Behavioural | Supportive Release Center (Treatment) |
| TASC Services Linkages - SRC OnsiteWhile at the SRC, individuals will meet with TASC Care Coordinators. Individuals will be screened for housing, health and behavioral health needs and then linked to appropriate community-based services. | Behavioural | Supportive Release Center (Treatment) |
| APN AppointmentIndividuals at the SRC will be able to meet with an Advanced Practice Nurse. As part of that visit, the APN will be able to prescribe medications or reroute prescriptions previously administered by the Cook County Jail's hospital, Cermak, to a participant's desired location as needed. | Behavioural | Supportive Release Center (Treatment) |
Primary outcome
Re-arrest count
Time frame: 365 days
Number of re-arrests within 365 days of study enrollment, measured at the individual level using Illinois State Police arrest records. Follow-up will begin the day an individual is first randomized (index randomization) and ITT group membership will be based upon index treatment assignment. Given expected dispersion and excess zeroes in the final dataset, the ITT treatment effect will be modeled using zero-inflated negative binomial regression. ITT analyses will be supplemented by a TOT analysis treating randomization as an instrument. Covariates for this outcome will include ordinal measures of arrest history (0, 1-2, 3-5, 6-10, and >10 arrests) and days incarcerated (0, 1-7, 8-14, 15-30, and >30 days) during the 365 days prior to index randomization.
4 secondary outcomes
Emergency department (ED) visits
Time frame: 365 days
Days until re-arrest
Time frame: 365 days
Re-arrest count, unique randomizations
Time frame: 365 days
Engagement with homelessness services
Time frame: 30 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Apr 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
David Meltzer, MD, PhD principal investigator
University of Chicago
Harold Pollack, PhD principal investigator
University of Chicago
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing TASC Service Linkages - Discharge Area Only, SRC Overnight Stay and TASC Services Linkages - SRC Onsite in people with Mental Health and Mental Health Services, run by University of Chicago at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 11 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Re-arrest count (time frame: 365 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Apr 2025; AzTrials last refreshed its copy on 27 Oct 2026.