CClinicalTrials.gg
CompletedNCT04273126Updated Jun 12, 2024

Helping Families Pilot of a Family Resilience Program for Families Experiencing Homelessness

An interventional study of Adapted Family Resilience Intervention in Family Relationship and Coping Skills, sponsored by University of California, Los Angeles. Completed at 1 site in United States. Open to participants aged 8 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-12.

Sponsored by University of California, Los Angeles · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
73
Allocation
Not applicable
Ages
8 Years and older
Sex
All
01

Study summary

The goal of this study is to pilot an adapted family resilience program among families with a recent history of homelessness in Los Angeles County and to assess for feasibility and acceptability. The investigators have adapted a family resilience program called Families Overcoming Under Stress (FOCUS), a trauma-informed intervention designed for families experiencing trauma, parental substance use, and homelessness. Our primary hypothesis is that the adapted family resilience program will be feasible and acceptable to families with a recent history of homelessness. Families that are eligible to participate in the study will be assigned to the adapted family resilience intervention. The intervention program consists of around 8-10 modules lasting up to one hour each. The program provides psychoeducation and teaches resilience skills including communication, problem solving, goal setting, and how to deal with stress. Families will be asked to fill out 3 surveys (one at the beginning of the program, one at the end of the program, and at 6 months follow-up). Some families may also be asked to participate in a hour long interview after the completion of the program for feedback on the program.

At this time, all assessments and intervention are being conducted remotely due to the pandemic.

02

Conditions studied

  • Family Relationship
  • Coping Skills

Keywords

  • resilience, psychological
  • homelessness
03

In context

Lead sponsor

University of California, Los Angeles is the lead sponsor of 1,142 studies on the registry; 192 are open to participants now.

Of its 91 completed or terminated interventional studies of FDA-regulated products, 66 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
8 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • English speaking
  • Family has a history of homelessness within the past two years (homelessness defined by the Department of Health and Human Services definition)
  • Parent/guardian/caregiver has custody of and cares for a youth between the ages of 8-17
  • Both youth and parent/guardian/caregiver are able to take part in an 8 module session intervention

Exclusion criteria

Exclusion Criteria:

  • Does not meet inclusion criteria
  • Has taken part in a Families OverComing Under Stress (FOCUS) intervention previously
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
73 participants (actual)

Study arms

  • Experimental
    Intervention

    This arm consists of approximately 8-10 modules lasting approximately one hour and consisting of psychoeducation and core components including communication, problem solving, goal setting, and dealing with stress, tailored to families with experiences of homelessness and parental substance use.

    Behavioral: Adapted Family Resilience Intervention

Interventions

  • BehavioralAdapted Family Resilience Intervention

    The program consists of approximately 8-10 modules lasting approximately one hour. Sessions focus on psychoeducation and key resilience skills.

06

What researchers measure

Primary outcomes

  1. Feasibility of the adapted family resilience intervention for families experiencing homelessness and parental SUDs through retention rates of participants.

    Feasibility is defined as the extent to which the adapted intervention can be implemented with families with an experience of homelessness and parental SUDs, assessed through measuring rate of retention of participants.

    Time frame: 6 months

  2. Feasibility of the adapted family resilience intervention for families experiencing homelessness and parental SUDs through completion of program core components.

    Feasibility is defined as the extent to which the adapted intervention can be implemented with families with an experience of homelessness and parental SUDs, assessed through measuring number of program core components completed by participants.

    Time frame: 3 months

  3. Acceptability of the adapted family resilience intervention to families experiencing homelessness and parental SUDs through qualitative interviews with youth and parents inquiring about intervention acceptability.

    The investigators will assess acceptability of implementing the adapted intervention with families experiencing homelessness and parental SUDs by conducting qualitative interviews with a subset of parent and youth participants completing the intervention. The interviews will explore acceptability of the intervention to families experiencing homelessness and parental substance use disorders and recommendations for improvement. The interviews will be audio-recorded, transcribed, and analyzed using thematic content analysis.

    Time frame: 3 months

  4. Acceptability of the adapted family resilience intervention through a self-report intervention acceptability measure.

    Acceptability is defined as the perception that the adapted intervention is agreeable and satisfactory.The investigators will administer a self-report measure of the acceptability of core components of the intervention to be completed following the intervention by parents and youth, with higher score indicating greater acceptability of the intervention to families experiencing homelessness and parental SUDs. Each individual item is scaled with a range of 1 (low) to 5 (high).

    Time frame: 3 months

Secondary outcomes

  1. Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST)

    Self reported measure administered to parents in the study to assess for substance use across lifetime and in the past 3 months. Each of the 8 item responses vary in scoring. The total substance involvement score (global continuum of risk) can be calculated by summing up the responses to all items. A higher score indicates higher risk for problems related to substance use.

    Time frame: Baseline, 3 month, 6 month

  2. Addiction Severity Index (ASI)

    Self reported measure administered to parents to assess for drug and alcohol use in the past 30 days and lifetime of regular use. The ASI does not yield a composite score but assesses days of use and extended periods of use.

    Time frame: Baseline, 3 month, 6 month

  3. General Anxiety Disorder (GAD-7)

    Self reported measure administered to parents to assess anxiety level. Each of the 7 item responses are scored from 0 (not at all) to 3 (nearly every day), yielding a total score ranging from 0-21. A higher score suggests higher level of anxiety.

    Time frame: Baseline, 3 month, 6 month

  4. Patient Health Questionnaire (PHQ-9)

    Self reported measure administered to parents to assess depression severity. Each of the 9 item responses are scored from 0 (not at all) to 3 (nearly every day), yielding a total score ranging from 0-27. A higher score suggests higher level of depression.

    Time frame: Baseline, 3 month, 6 month

  5. PTSD Checklist for the DSM-V (Diagnostic and Statistical Manual)

    Self-reported measure administered to parents that assesses the severity of PTSD symptoms over the past month. The PTSD Checklist for DSM-5 (PCL-5), the responses are scored from 0 (not at all) to 4 (extremely). To assess total symptom severity, scores for each of the 20 items are summed, the range is 0-80, with higher levels indicating higher severity.

    Time frame: Baseline, 3 month, 6 month

  6. Short Form 12 (SF-12)

    Self reported measure administered to parents to assess health and well-being. The SF-12 is scored as physical (PCS-12) and mental (MCS-12) component summary scales. The PCS-12 and MCS-12 scores use norm-based scoring with 50 being the population mean. The possible scores for PCS-12 and MCS-12 could range from 0 (worst) to 100 (best), with scores above and below 50 being above and below average.

    Time frame: Baseline, 3 month, 6 month

  7. Connor-Davidson Resilience Scale (CD-RISC)

    Self reported measure administered to parents to assess resilience. Each of the 10 item responses are scored from 0 (not true at all) to 4 (true nearly all of the time), yielding a total score that ranges from 0-40. A higher score indicates more resilience.

    Time frame: Baseline, 3 month, 6 month

  8. Medical Outcomes Study Social Support Survey (MOS-SSS)

    Self-reported measure administered to parents to assess social support. Each of the of 8 item responses are scored from 1 (none of the time) to 5 (all of the time), yielding a total score that ranges from 8-40. A higher score for an individual scale or for the overall support index indicates more support.

    Time frame: Baseline, 3 month, 6 month

  9. Monitoring the Future Scale (Substance Use Scale)

    Self reported measures to assess substance use in the past 30 days and lifetime for youth for each selected substance. For the 29 items, responses range from from "0 occasions of use" to "40 or more occasions of use."

    Time frame: Baseline, 3 month, 6 month

  10. Monitoring the Future Scale (Perceived Risk Scale)

    Self reported measure to assess perceived risks of substance use for youth for each selected substance. For the 6 items, each response ranges from "no risk" to "great risk", with the option to select "can't say, drug unfamiliar."

    Time frame: Baseline, 3 month, 6 month

  11. Monitoring the Future Scale (Disapproval Scale)

    Self reported measure to assess disapproval of substance use for youth. For each of the 17 items, responses range from "not disapprove" to "strongly disapprove."

    Time frame: Baseline, 3 month, 6 month

  12. Strength and Difficulties Questionnaire (SDQ)

    Self reported measure to assess psychological strengths and difficulties of children/youth. Parents will complete the measure for their children. The measure will also be delivered to youth (age 11-14). Each of the 25 item responses are scored from 0 (not true) to 2 (certainly true). The items are divided into 5 subscales (emotional problems, conduct problems, hyperactivity, peer problems, and prosocial). The first four subscales refer to difficulties that children may have and may be group together in a general subscale of difficulties (20 items). The subscale of prosocial skills refer to positive and adaptive behaviors. For each of the 5 subscales, the score can range from 0-10. The score of the difficulties subscale ranges from 0 to 40. Higher scores suggest higher emotional and behavioral symptoms.

    Time frame: Baseline, 3 month, 6 month

  13. Screen for Child Anxiety Related Emotional Disorders (SCARED)

    Self reported measure to assess childhood anxiety disorders, including panic, generalized anxiety, separation anxiety, social phobia, and school phobia among children . Each of the 41 item responses are scored from 0 (not true or hardly ever true) to 2 (very true or often true), yielding a total score ranging from 0-82.

    Time frame: Baseline, 3 month, 6 month

  14. Mood and Feelings Questionnaire (MFQ)

    Self reported measure to assess depression in children and youth. Each of the 13 item responses are scored from 0 (not true) to 2 (true), yielding a total score ranging from 0-26. A higher score suggests more severe depressive symptoms.

    Time frame: Baseline, 3 month, 6 month

  15. Resistance to Peer Influence Scale

    Self reported measure to assess resistance to peer influence for youth.The measure presents respondents with a series of 10 pairs of statements and asks them to choose the statement that is the best descriptor. After indicating the best descriptor, the respondent is then asked whether the description is "Really True" or "Sort of True." Responses are then coded on a 4-point scale, ranging from "Really true" for one descriptor to "Really true" for the other descriptor, and averaged. A higher score suggests greater resistance to peer influence.

    Time frame: Baseline, 3 month, 6 month

  16. Children's Coping Strategies Checklist-Revision 1 (CCSC-R1)

    Self reported measure to assess coping strategies among youth. Each of the 54 item responses are scored from 1 (never) to 4 (always). Scoring for the four major factors of coping is reached by taking the mean.

    Time frame: Baseline, 3 month, 6 month

  17. Resilience Youth Development Module (RYDM) of the California Healthy Kids Survey (CHKS)

    Self reported measure to assess internal assets for children and youth. Each of the 12 item responses are scored from 1 (not at all true) to 4 (very much true), yielding a score that ranges from 12 to 48. A higher score indicates higher levels of internal assets.

    Time frame: Baseline, 3 month, 6 month

  18. Deviant Peer Affiliation Scale

    Self reported measure to assess deviant peer affiliations for youth (age 12-14). Each of the 3 item responses are scored from 1 (very few) to 5 (almost all), with the exception of one reverse-coded item. The total score is computed by averaging across all items. A higher score suggests greater deviant peer affiliations.

    Time frame: Baseline, 3 month, 6 month

  19. McMaster Family Assessment Device (FAD)

    Self reported measure to assess family functioning for parents and youth over 12. Each of the 12 item responses are scored from 1 (strongly agree) to 4 (strongly disagree). The scores are added up and then divided by the number of items, giving a total score ranging from 1 to 4. A higher score indicates worse functioning.

    Time frame: Baseline, 3 month, 6 month

  20. Parental Sense of Competence Scale (PSOC)

    Self reported measure for parents to assess parenting self-esteem. Each of the 17 item responses are scored from 1 (strongly disagree) to 6 (strongly agree), yielding a total score that ranges from 17-102. A higher score suggests greater self-esteem.

    Time frame: Baseline, 3 month, 6 month

  21. Parental Monitoring Scale

    Self reported measure to assess adolescents' perception of their parents' monitoring. Each of the 6 item responses are scored from 1 (never) to 5 (always). A composite score is obtained by averaging responses to the 6 items. A higher score indicates higher perceived perception of parent monitoring. This scale is also delivered to parents, in order to assess the parent's perception of their supervision. A composite scale score is obtained in the same manner. Higher score indicates higher perceived perception of their monitoring.

    Time frame: Baseline, 3 month, 6 month

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Study locations

1 site
  • UCLA
    Los Angeles, California 90095, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04273126
Lead sponsor
University of California, Los Angeles
Collaborators
National Institute on Drug Abuse (NIDA), American Academy of Child Adolescent Psychiatry.
Responsible party
Roya Ijadi-Maghsoodi, MD, MSHPM (Assistant Professor in Residence, University of California, Los Angeles) — Principal investigator
First posted
Feb 17, 2020
Start date
Feb 19, 2020
Primary completion
Apr 3, 2023
Completion
Apr 3, 2023
Last update
Jun 12, 2024

Study contacts

Roya Ijadi-Maghsoodi, MD, MSHPM
principal investigator · University of California, Los Angeles

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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