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Homeless Youth Study - Stepping Stone 2.0

Not Applicable
Completed
Conditions
Mental Health Issue (E.G., Depression, Psychosis, Personality Disorder, Substance Abuse)
Interventions
Behavioral: Mobile self-help intervention
Registration Number
NCT03776422
Lead Sponsor
Rush University Medical Center
Brief Summary

Housing instability is both a cause and consequence of mental health problems. As such youth experiencing housing instability (e.g., homeless or marginally housed) have higher rates of mental health problems.Because of their circumstances, these youth also face significant barriers to mental health care and are therefore less likely to receive the treatment that they need. Mobile technology may offer a novel platform for increasing access to mental health care in this population. The primary goals of this pilot study are to (1) establish the feasibility and acceptability of delivering automated mental health interventions via smartphone technology, (2) examine the extent to which automated mental health interventions delivered via mobile technology improve mental health in homeless, marginally-housed, and exiting foster youth.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • 16-25 years

  • English-speaking

  • Youth must meet one of the following risk criteria

    • Experiencing housing instability as defined by:

      • lacking a fixed, regular, and adequate nighttime residence OR whose primary nighttime residence is a shelter, institution, or a "public or private place not designed for, or ordinarily used as, a regular sleeping accommodation for human beings"
      • sharing the housing of other persons due to loss of housing [or] economic hardship.
      • frequent moves, poor housing quality (e.g., living in severely overcrowded housing).
    • Imminently leaving the foster care system

  • Willingness and ability to comply with requirements of the study protocol

Exclusion Criteria

* Inability to understand study procedures and participate in the informed consent process.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Mobile self-help interventionMobile self-help interventionThis study uses automated self-help interventions designed as a kit of smartphone tools.
Primary Outcome Measures
NameTimeMethod
Program adherenceBaseline to Endpoint (6 months)

Program adherence will be assessed based on usage data determining how often participants utilized the study applications, and how often they completed daily surveys and rated daily tips.

Program satisfactionMidpoint (3 months) and Endpoint (6 months)

Program satisfaction will be assessed using a self-report questionnaire that participants will be asked to complete at the midpoint and endpoint of the study. Participants will be asked to report the extent to which they benefited from the study, how helpful the mobile applications were, and if they would recommend the study to others. These responses are recorded on 5-point likert type scales with higher ratings indicating higher satisfaction.

Secondary Outcome Measures
NameTimeMethod
Anxiety symptomsBaseline (0 months), Midpoint (3 months), Endpoint (6 months)

Anxiety symptoms will be assessed using the adaptive PROMIS Bank v1.0 for anxiety.

Alcohol useBaseline (0 months), Midpoint (3 months), Endpoint (6 months)

Alcohol use will be assessed using the Alcohol Use Disorders Identification Test (AUDIT-C).

Cannabis useBaseline (0 months), Midpoint (3 months), Endpoint (6 months)

Cannabis use will be assessed using the Cannabis Use Disorder Identification Test - Revised (CUDIT-R).

Risky sexual behaviorBaseline (0 months), Midpoint (3 months), Endpoint (6 months)

Risky sexual behaviors will be assessed using the sexual behavior items from the Centers for Disease Control and Prevention's Youth Risk Behavior Survey (2011).

Satisfaction with life: Satisfaction with Life Scale (SWLS)Baseline (0 months), Midpoint (3 months), Endpoint (6 months)

General satisfaction with life will be assessed using the Satisfaction with Life Scale (SWLS). This measure is 5 items, with each item rated on a scale from 1-7. All 5 items are summed to achieve a total score of 5-35. Higher scores indicate higher satisfaction with one's life circumstances.

PTSD symptomsBaseline (0 months), Midpoint (3 months), Endpoint (6 months)

PTSD symptoms will be assessed using the The Primary Care PTSD Screen for DSM-5 (PC-PTSD-5).

Psychosocial flourishingBaseline (0 months), Midpoint (3 months), Endpoint (6 months)

Psychological resources and strengths will be assessed using the Flourishing Scale (FS). This measure is 8 items, with each item rated on a scale from 1-7. All 8 items are summed to achieve a total score of 8-56. Higher scores indicate that an individual has more psychological resources and strengths.

Depression symptomsBaseline (0 months), Midpoint (3 months), Endpoint (6 months)

Depression symptoms will be assessed using the adaptive PROMIS Bank v1.0 for depression.

Trial Locations

Locations (1)

Rush University Medical Center

πŸ‡ΊπŸ‡Έ

Chicago, Illinois, United States

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