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NCT05259436 · ClinicalTrials.gov registry record · NA
Collaborative Approach to Examining Adversity and Building Resilience Study
A NA study of Caregiver Stress and Early Life Adversity, sponsored by University of California, San Francisco.
- Active
- Registry status
- NA
- Development phase
- 300
- Enrollment target
- 4
- Study locations
NCT05259436: Active NA study of Caregiver Stress and Early Life Adversity, sponsored by University of California, San Francisco.
NCT05259436 is a NA study of Caregiver Stress and Early Life Adversity that is active but no longer recruiting, run by University of California, San Francisco. The registered enrollment target is 300 participants, above the 168-participant average among 5 other Caregiver Stress trials with a reported enrollment target (79% higher). The trial reports 4 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05259436, a NA study of Caregiver Stress and Early Life Adversity, is active but no longer recruiting, sponsored by University of California, San Francisco.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 300 participants
- Enrollment target
- 4
- Study locations
Study Summary
To examine the behavioral, psychosocial, and biologic impact of resilience-promoting interventions associated with primary care.
Primary Outcome
Caregiver reported survey validated measure of parenting stress. The Parenting Stress Index - Short Form (PSI) is a 36-item self-report measure completed by parents to measure stress level within the context of parenting. Participants respond to items on a 5-point Likert scale. Responses to each item in a sub-category are totaled to calculate three subcategory scores, which are summed to represent a total parenting stress score. Higher scores indicate higher levels of parenting stress.
Conditions Studied
Interventions
- BEHAVIORAL Caregiver-child Intervention
- BEHAVIORAL Enhanced Primary Care
Study Locations (4)
California
- UCSF Benioff Children's Hospital Oakland - Oakland
- LifeLong Medical Care - Richmond
- Zuckerberg San Francisco General Hospital and Trauma Center - San Francisco
- Santa Barbara Neighborhood Clinics - Santa Barbara
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2022-04-11 |
| Est. Completion | 2025-06-30 |
| Phase | NA |
What the registry record for NCT05259436 still lists
NCT05259436 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, above the 168-participant average among 5 other Caregiver Stress trials with a reported enrollment target (79% higher).
The record links to 2 conditions, with Caregiver Stress appearing as the primary indexed condition, and to 2 interventions - of which Caregiver-child Intervention is the first listed.
NCT05259436 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT05259436 about?
NCT05259436 is a clinical study titled "Collaborative Approach to Examining Adversity and Building Resilience Study". To examine the behavioral, psychosocial, and biologic impact of resilience-promoting interventions associated with primary care.
What is the current status of trial NCT05259436?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 300 participants. The study started on 2022-04-11. Estimated completion is 2025-06-30.
What conditions does trial NCT05259436 study?
This clinical trial studies the following conditions: Caregiver Stress, Early Life Adversity.
What interventions are being tested in trial NCT05259436?
The interventions under investigation include: Caregiver-child Intervention (BEHAVIORAL), Enhanced Primary Care (BEHAVIORAL).
Who is sponsoring clinical trial NCT05259436?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05259436 being conducted?
This trial has 4 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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