NRF for Improved Re-Entry Outcomes for Offenders With Brain Injury (Brain Injury RE)

Sponsor
Icahn School of Medicine at Mount Sinai (Other)
Overall Status
Recruiting
CT.gov ID
NCT05708092
Collaborator
Brain Injury Association of Pennsylvania (Other)
765
2
2
44.4
382.5
8.6

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the effectiveness of NeuroResource Facilitation, a novel/innovative intervention, in reducing recidivism in offenders with brain injury (BI).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: NeuroResource Facilitation (NRF)
N/A

Detailed Description

The prevalence of brain injury (BI) is significantly greater in justice-involved populations, and a substantial proportion of prisoners have likely experienced a BI during their lifetime. A history of BI has a statistically significant association with increased use of correctional, medical and psychological services including crisis intervention; an increased frequency of institutional misconducts; and higher recidivism rates. Brain injury in justice-involved populations is frequently undiagnosed, and therefore untreated, which contributes to the cycle of recidivism. Identifying BI opens up new resources to ex- offenders that can more effectively help them to become productive in their lives in the community. In partnership with the Icahn School of Medicine at Mount Sinai, the Brain Injury Association of Pennsylvania, and the Pennsylvania Department of Corrections (PADOC), this project will implement a randomized clinical trial to determine if a case management intervention called Neurorehabilitation Facilitation (NRF) is effective in reducing recidivism by ten percent in offenders with acquired BI. Offenders in two Pennsylvania prisons (State Correctional Institution (SCI) sites in PA, SCI Phoenix, SCI Chester, SCI Frackville, and SCI Mahanoy) will be screened for BI and cognitive impairment, and those who screen positive will be randomized to receive the intervention or to receive standard of care (SoC). Two thirds of those randomized will receive the intervention and the remaining one third will serve as controls. All participants will be followed for up to three years following their release to examine the immediate and long-term reduction in recidivism.

The primary hypothesis is that NRF, as compared to SoC, will result in a 10% reduction in average 1-year recidivism, estimated by the 2013

Department of Corrections (DOC) report as 35-38%. Understanding that additional factors will contribute to the effect of NRF, the required sample was based on the primary analysis, a logistic regression of the binary response variable recidivism, adjusted for additional independent variables (described below) in the model with estimated R-squared=0.10. An effect size of 10% reduction corresponds to an odds ratio in this model of 0.643. With two thirds (67%) of cases randomized to NRF, and one third (33%) randomized to SoC, a total sample of N=688 provides 80% power at alpha set at 0.05. Anticipating that there will be a loss of approximately 10% of randomized cases to attrition, N=764 cases will be randomized, with n=509 cases randomized to NRF and 255 randomized to SoC.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
765 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Masking Description:
Only the follow up data collector will be blinded to the randomization assignment of all participants. At the beginning of each interview, the participant will be instructed to not share whether they were assigned to a NRF or SOC.
Primary Purpose:
Treatment
Official Title:
NeuroResource Facilitation for Improved Re-Entry Outcomes for Offenders With Brain Injury: A Multi-Site Randomized Controlled Trial.
Actual Study Start Date :
Mar 22, 2022
Anticipated Primary Completion Date :
Dec 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: NeuroResource Facilitation

As part of the NRF intervention group, participants will receive specialized care management, both in prison and after the participant goes home. While in the State Correctional Institution (SCI), participants will meet weekly to monthly depending on resource needs, and how close participant is to release with a NeuroResource Facilitator in person who will help participants to understand more about their challenges. Participants may also be referred to a group run by the Facilitator in conjunction with staff from the prison. The facilitator will also tell the participant about resources that are available to help after the participant's release and help participants get connected to them.

Behavioral: NeuroResource Facilitation (NRF)
NRF is defined as a specialized service that promotes access to services and coordinates care specific to the needs of individuals with brain injury. Possible resources include vocational services, medical assistance, Social Security (SSI or SSDI if appropriate), and other organizations that can support reentry. If needed to gain access to services and organizations, the facilitator will also provide participants with a summary that includes results from brain injury screenings questionnaire, neurocognitive (thinking abilities) tests, and symptoms. The researchers will share information and coordinate with prison and parole staff about participation in the study. Participant's information will also be shared with resources that could help participants after release, such as funding sources and brain injury services. After release from SCI, the NRF facilitator will assist the participant with all the preparation and logistics associated with the resources the participant applied to.

No Intervention: Standard of Care

As part of the SoC, participants will receive the re-entry services normally receive if not in the study including (but not limited to) Treatment Services, Educational and Vocational Training, Mental Health Management, Reentry and Transitional Services, Population Management and Community Corrections.

Outcome Measures

Primary Outcome Measures

  1. Number of Recidivism [at year 1]

    According to the PADOC, rearrest is measured as the first instance of arrest after inmates are released from state prison and reincarceration is measured as the first instance of returning to state prison after an offender is released from state prison. Overall recidivism is measured as the first instance of any type of rearrest or reincarceration after inmates are released from state prison.

  2. Number of Recidivism [at year 3]

    According to the PADOC, rearrest is measured as the first instance of arrest after inmates are released from state prison and reincarceration is measured as the first instance of returning to state prison after an offender is released from state prison. Overall recidivism is measured as the first instance of any type of rearrest or reincarceration after inmates are released from state prison.

Secondary Outcome Measures

  1. Number of Productive Activities Hours [up to 36 months post release]

    Productive Activities Hours include competitive employment (hours worked), and volunteer work (hours worked), brain injury clubhouses (hours attended), vocational training program (hours attended), and education (hours attended).

  2. Number or Participants Engaged in Productive Activity [up to 36 months post release]

    The number of participants who engage in vocational training program or education activity at end of program.

  3. Number of Participants Engaged with Services [up to 36 months post release]

    Engagement with Services. Engagement with Services includes community-based specialized NeuroRehabilitation services (physical therapy, occupational therapy, speech therapy, cognitive rehabilitation therapy, neuropsychology), and vocational rehabilitation services (job development, job placement, job coaching).

  4. Number of Participants Connected to Health/Medical Resources [up to 36 months post release]

    The connection to Health/Medical resources will also be measured, "safety net" resources (SNAP, MA, SSI, food bank, etc).

  5. Number of participants in Community Support [up to 36 months post release]

    Community Support - Participation in support groups and recovery resources, including religious activities, recreation, and access to transportation.

  6. Number of Participants in Stable Housing [up to 36 months post release]

    Community Support - whether the ex-offender has stable housing

  7. Number of Parole Obligations Met [up to 36 months post release]

    Parole Obligations - the extent to which the ex- offender has satisfied the obligations of Parole will be tracked, such as whether they have completed all mandated treatment

  8. Number of Participants Discharged from Supervision [up to 36 months post release]

    Number of participants that have been or (are likely to be) discharged from supervision.

  9. Date of Reception [up to 36 months post release]

    The day on which an individual was initially received into the custody

  10. Date Committed [up to 36 months post release]

    The day on which an individual was committed to sentenced

  11. Date of entry into Department of Corrections [up to 36 months post release]

    The day on which an individual was admitted into the Department of Corrections

  12. Number of Participants with particular Classification of Offense [up to 36 months post release]

    Number of Participants with particular Classification of Offense as listed by the Department of Corrections

  13. Number of participants who are Guilty but mentally ill [up to 36 months post release]

    Number of participants who are guilty but mentally ill

  14. Number of Participants Recommended for aftercare [up to 36 months post release]

    Number of Participants Recommended to receive aftercare

  15. Status of Participants after Program completion [up to 36 months post release]

    Status of Participants after Program completions as determined by the Department of Corrections

  16. Program category [up to 36 months post release]

    Program category as as determined by the Department of Corrections

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18+ years old

  • Proficient in English

  • History of brain injury (OSU-TBI-ID)

  • Significant cognitive impairment (RBANS and Trails A&B)

  • Within 6 months of release

  • Returning to 6 county area (Bucks, Chester, Delaware, Montgomery, Philadelphia and Schuylkill)

Exclusion Criteria:
  • Non-English Speaking

  • Under 18 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 Icahn School of Medicine at Mount Sinai New York New York United States 10065
2 Brain Injury Association of Pennsylvania Carlisle Pennsylvania United States 17015

Sponsors and Collaborators

  • Icahn School of Medicine at Mount Sinai
  • Brain Injury Association of Pennsylvania

Investigators

  • Principal Investigator: Maria Kajankova, PhD, Icahn School of Medicine at Mount Sinai

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Maria Kajankova, Associate Professor, Icahn School of Medicine at Mount Sinai
ClinicalTrials.gov Identifier:
NCT05708092
Other Study ID Numbers:
  • STUDY-21-00561
  • 2020-75-CX-0007
First Posted:
Feb 1, 2023
Last Update Posted:
Feb 1, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 1, 2023