Autism Spectrum Disorder Clinical Trial
Official title:
Developing a Culturally Adapted Intervention for Latino Youth Transitioning to Adulthood
The purpose of this study is to evaluate the acceptability, feasibility (e.g., satisfaction, completion rate, barriers to recruitment, treatment fidelity) of the culturally refined Launching! to Adulthood (¡Iniciando! la Adultez) program, to test for a preliminary signal of effect between baseline and post-treatment for the Launching! to Adulthood (¡Iniciando! la Adultez) program and to identify preliminary neural mechanisms of action, including biomarkers of brain structure and connectivity, in terms of treatment response for 15 Latino young adults participating in the ¡Iniciando! therapy program.
| Status | Recruiting |
| Enrollment | 58 |
| Est. completion date | January 31, 2025 |
| Est. primary completion date | April 30, 2024 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 25 Years |
| Eligibility | Inclusion Criteria: - confirmed case of ASD - a score of >14 on the Social Communication Questionnaire-Lifetime (SCQ-L110) completed with the mother or father - meet DSM-5 criteria for ASD based on a Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 ASD symptom checklist - previous diagnosis of ASD from a licensed mental health or medical professional - speak English - have a parent willing to participate (treatment group only) - score >85 on verbal intelligence quotient (IQ) on the Kaufman Brief Intelligence Test (KBIT-2) Exclusion Criteria: - history of a psychotic disorder or current psychotic symptoms - suicidal ideation with intent or plan - current alcohol or other substance use disorder rated severe - concurrent enrollment in another clinical trial for autism spectrum disorder - expression of unwillingness to complete study procedures - For fMRI, unable to undergo fMRI scanning due to metallic devices or objects (cardiac pacemaker or neurostimulator, some artificial joints, metal pins, surgical clips, or other implanted metal parts) or claustrophobic to the scanner. |
| Country | Name | City | State |
|---|---|---|---|
| United States | The University of Texas Health Science Center at Houston | Houston | Texas |
| Lead Sponsor | Collaborator |
|---|---|
| The University of Texas Health Science Center, Houston | UTHealth Houston Seed Grant and Autism Speaks Fellowship |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in adaptive behavior as assessed by the Adaptive Behaviour Assessment System, Third Edition | This is a 239 item questionnaire and each is scored from 0(is not able to do this behavior) to 3 [(always able to do this behavior)(or almost always)] a higher number indicating better outcome | baseline, mid-treatment (5 weeks after baseline) , post-treatment (10 weeks after baseline), 3 month follow up, 6 month follow up | |
| Primary | Change in Quality of life as assessed by the Autism Spectrum Quality of Life (ASQoL) questionnaire | This is a 9 item questionnaire. Questions 1-5 and 9 are each scored from 1(not at all) to 5(totally) a higher number indicating better outcome and questions 6-8 are reverse scored from 5(never) to 1(always) a higher score indicating worse outcome | baseline, mid-treatment (5 weeks after baseline) , post-treatment (10 weeks after baseline), 3 month follow up, 6 month follow up | |
| Primary | Change in Anxiety as assessed by the Generalized Anxiety Disorder-7 (GAD7) | This is a 7 item questionnaire and each is scored from 0(not at all) to 4(nearly every day) for a maximum score of 21 , higher score indicating more anxiety | baseline, mid-treatment(5 weeks after baseline) , post-treatment (10 weeks after baseline), 3 month follow up, 6 month follow up | |
| Primary | Change in depression as assessed by the Patient Health Questionnaire (PHQ-9) | This is a 9 item questionnaire and each is scored from 0(not at all) to 3(nearly every day) for a maximum score of 27, higher number indicating worse outcome | baseline, mid-treatment(5 weeks after baseline) , post-treatment (10 weeks after baseline), 3 month follow up, 6 month follow up | |
| Secondary | Change in caregiver burden as assessed by the Rapid Screen for Caregiver Burden (CBI) | This is a 24 item questionnaire, each item is given a score between 0 (not at all descriptive) and 4 (very descriptive), where higher scores indicate greater caregiver burden | baseline, mid treatment (5 weeks after baseline) , post-treatment (10 weeks after baseline), 3 month follow up, 6 month follow up | |
| Secondary | Change in efficacy of coping with life's challenges as assessed by the Coping Self-Efficacy Scale (CSES) | This is a 26 item questionnaire and each is scored on a 11-point scale from 0(cannot do at all)-10 (certain can do) and higher number indicates better outcome | baseline, mid treatment (5 weeks after baseline) , post-treatment (10 weeks after baseline),3 month follow up, 6 month follow up | |
| Secondary | Change in stress as assessed by the Riverside Acculturation Stress Inventory (RASI) | This is a 15-item scale and each is scored on a 5-point scale ranging from 1 (strongly disagree) to 5 (strongly agree) higher number indicates worse outcome | baseline, mid treatment (5 weeks after baseline) , post-treatment (10 weeks after baseline), 3 month follow up, 6 month follow up | |
| Secondary | Change in goal attainment Goal Attainment Scaling (GAS) | This is scored on a 5-point scale, with the degree of attainment captured for each goal area: If the patient achieves the expected level, this is scored at 0. If they achieve a better than expected outcome this is scored at: +1 (somewhat better) +2 (much better) If they achieve a worse than expected outcome this is scored at: -1 (somewhat worse) or -2 (much worse) Goals may be weighted to take account of the relative importance of the goal to the individual, and/or the anticipated difficulty of achieving it. | week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 9, week 10 |
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