Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05372978
Other study ID # H21-02584
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2, 2022
Est. completion date December 2023

Study information

Verified date May 2022
Source University of British Columbia
Contact Jiaying Zhao, PhD
Phone 604-827-2203
Email jiayingz@psych.ubc.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary goal of the study is to determine the impacts of a one-time unconditional cash transfer on the well-being of people experiencing homelessness.


Description:

The goal of this project is to examine the effect of cash-transfers for people experiencing homelessness in Metro Vancouver. In partnership with Foundations for Social Change, we will distribute a one-time unconditional cash transfer of $8,500 to each of the 200 participants, with 200 additional participants in a control group who will not receive the cash transfer. To evaluate the effect of the cash transfer, participants will complete surveys 1, 2, 3, 6, 9, and 12 months after the cash transfer, and we will track important life outcomes such as housing, employment, health, cognitive function, and well-being.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. Participants must be homeless at the time of recruitment. 2. Participants must be between 18 and 65 years of age, inclusive. 3. Participants must be a Canadian citizen or permanent resident in Canada Exclusion Criteria: The following participants will be excluded: 1. Participants who report severe problematic substance use (score = 6 on DAST). 2. Participants who report severe problematic alcohol use (score = 20 on AUDIT). 3. Participants who report severe psychiatric symptoms (score above 2 on item 5 or above 4 on items 13 or 14 on CSI). 4. Participants who report problematic gambling behavior (score = 8 on PGSI).

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cash transfer
Participants will receive a one-time unconditional cash transfer of $8,500.

Locations

Country Name City State
Canada University of British Columbia Vancouver British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Foundations for Social Change

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stable housing Number of days spent in stable housing. 1-3 months
Primary Homelessness Number of days spent homeless. 1-3 months
Primary Savings Total value of financial assets. 1-3 months
Primary Total Spending Amount of money spent on regular and one-time purchases. 1-3 months
Primary Spending on Rent Amount of money spent on rent. 1-3 months
Primary Spending on temptation goods Amount of money spent on temptation goods, such as drugs, alcohol, and cigarettes. 1-3 months
Primary Cost of shelter use Estimated societal cost of shelter use based on number of days staying in shelter 1-3 months
See also
  Status Clinical Trial Phase
Completed NCT02793739 - Hyaluronic Acid Filler for Dorsal Finger Volume Loss N/A
Not yet recruiting NCT02426528 - R.CULT.HEA - URban Environment, CULTural Social Use of Space and HEAlth / Well-being Effect on Population N/A
Terminated NCT02036697 - Hemodynamic Effects of Low Dose Spinal Anesthesia for Cesarean Section N/A
Completed NCT02011035 - Evaluating the Clinical Efficacy and Safety of Colflex Phase 1
Completed NCT02762916 - CONTECI Program: A New Way to Control Peripheral Arterial Disease Using New Technologies N/A
Completed NCT01874132 - Study of the Long-term Effects of Exercise on Heath Indicators in Older People N/A
Completed NCT01373541 - Effect of InFatâ„¢ Product on Stool Biochemistry and Stool Characteristics in Formula-fed Term Infants in China N/A
Completed NCT05264844 - Peripheral Venous Catheter and Masking Tape N/A
Completed NCT03037112 - Resetting the Default: Improving Provider-patient Communication to Reduce Antibiotic Misuse N/A
Completed NCT03116607 - Pharmaceutical Intervention Program at Readmission and User Satisfaction in a Emergency Department N/A
Completed NCT04935541 - Dexmedetomidine vs. Remifentanil Undergoing Cataract Surgery in Geriatrics N/A
Completed NCT03360773 - Emotional Fluctuations in the Flow of Daily Life. Ecological Analysis of Depressive Symptoms in the General Population.
Active, not recruiting NCT02459327 - Integrated Model for Promoting Parenting and Early School Readiness in Pediatrics N/A
Not yet recruiting NCT06416943 - 3D Port-A Catheter Model for New Staff N/A
Active, not recruiting NCT05284591 - Non-interventional Study to Evaluate Patient and Healthcare Provider Satisfaction of Daratumumab Use in the Treatment of First-line Daratumumab, Lenalidomide, Dexamethasone (DRd) Multiple Myeloma Patients in Germany Depending on Application Route (sc or iv)
Completed NCT05953870 - This is a Study to Evaluate if Music Therapy Can Reduce Stress and Increase Satisfaction of Patients Undergoing Ambulatory Surgery N/A
Not yet recruiting NCT02929173 - Effect of Different Types of Crowns on Patient Satisfaction and Clinical Assesment Phase 2
Completed NCT04757428 - Clinical Evaluation of Lithium Disilicate (e.Max) and Hybrid Nano-ceramic (Grandio) CAD/CAM Endocrowns N/A
Completed NCT02696122 - Quality of Recovery After General or Spinal Anesthesia for Inguinal Hernia Repair N/A
Completed NCT00874068 - The Effects of Dietary Palmitic Acid Triacylglyceride Position on Bone Strength Parameters in Infants N/A