NCT06486584Completed
Contingency Management for Problematic Behavior Reduction in the Community
Source: ClinicalTrials.gov · Last updated 4 Mar 2025
Brief summary (registry, in English)
This study aims to determine the feasibility and effectiveness of implementing a contingency management program in a small group of mentally ill, unhoused individuals with schizophrenia or bipolar disorder and anosognosia (a lack of insight into their mental health) in the City of Tulsa. The primary objective of the study is to decrease disruptive or problematic behaviors (e.g. interactions with police, emergency services, hospitals, shelter staff, 911 calls) by unhoused individuals in the community through monetary incentives. Up to 15 participants will meet weekly for 30 minutes with their case manager to discuss progress on life goals ($10) and for having seven days with no disruptive behaviors (or "trouble-free days") per week at each visit, they will receive an additional baseline payment of $20, increasing with continued success in subsequent weeks by $1 per week.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 15 (actual)
- First submitted
- 27 Jun 2024
- Start date
- 20 Jun 2023
- Primary completion date
- 15 Dec 2023
- Lead sponsor
- Laureate Institute for Brain Research, Inc.
- Diseases
- Schizophrenia, Bipolar disorder
- NCT number
- NCT06486584
What you commit to
- Study type: Interventional
- Participants enrolled: 15
- From 20 Jun 2023 to the primary completion date, 15 Dec 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Unstable medical conditions that would interfere with participation
- Cognitive impairment that would interfere with participation in the study
- History of severe aggression or violent behavior posing a risk to study staff or other participants
- Active suicidal ideation or a history of suicide attempts within the past 12 months
Other
- Inability to provide informed consent
Who the study is looking for
- Age 18-65 years old
- Diagnosis of Schizophrenia Spectrum, Bipolar, or Related Disorders
- Presence of Anosognosia (SUMD: Minimum combined score of 4 on questions 1) and 2); Recent (at least \<6 months) history of disruptive behaviors (at least 1 disruptive behavior per week in \>50% of weeks in the 6-month period prior to enrollment)
- Receive case management services through TDC
- Ability to comply with study procedures
- Willingness to participate in contingency management intervention
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Laureate Institute for Brain Research Coordinator of this site? Confirm its status | Tulsa | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.