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N/A N=8 Treatment

Social Work Assistance and Stipends for Housing (SASH)

Opioid-Related Disorders · Housing Problems

Enrolled (actual)
8
Serious AEs
0.0%
Results posted
Apr 2025
Primary outcome: Primary: Methadone Doses — 4.58 percent of missed doses

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Stipend and Social Work Supports (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Maryland, Baltimore
Primary completion
Jan 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Methadone Doses
34.11
PRIMARY
Methadone Doses
34.11
PRIMARY
Methadone Doses
34.11
PRIMARY
OUD Checklist Scores
7.2
PRIMARY
OUD Checklist Scores
7.2
PRIMARY
OUD Checklist Scores
7.2
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Urine Toxicology Tests
3
PRIMARY
Quality of Life Scores
32
PRIMARY
Quality of Life Scores
32
PRIMARY
Quality of Life Scores
32
PRIMARY
Housed vs Unhoused at 6 Months
3 .125
PRIMARY
Housed vs Unhoused at 6 Months
3 .125

Summary

SASH is a clinical trial feasibility study that will provide an intervention to improve Opioid Use Disorder (OUD), Quality of Life (QOL), and housing outcomes for homeless patients receiving Medication for Opiate Use Disorder (MOUD). The main questions of the study are does a $500 housing stipend for individuals on MOUD increase treatment retention, improved quality of life and prevent homelessness.

Eligibility Criteria

Inclusion Criteria

  • Experienced homelessness during at least 15 of the 30 days preceding enrollment
  • Is a patient at the University of Maryland Addiction Treatment Program (ATP) receiving methadone treatment.

Exclusion Criteria

-

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05803603). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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