The Resilience Clinic Evaluation

Caregiver Stress Clinical Trial

Official title:

The Resilience Clinic: Program Evaluation and Quality Improvement

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05690256
• Other study ID #: 22-37781
• Status: Recruiting
• Phase: N/A
• Start date: May 25, 2023
• Est. completion date: November 30, 2023

Study information

• Verified date: May 2023
• Source: University of California, San Francisco
• Contact: Joan J Jeung, MD
• Phone: 415-353-8835
• Email: Joan.Jeung[@]ucsf.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Early life adversity can affect children's physical and mental health. The Resilience Clinic is a support program for young children and their caregivers who have been exposed to significant adversity, aiming to prevent the harmful effects of stress and improve child health, behavior, and development while also reducing caregiver stress. This study seeks to evaluate the Resilience Clinic, assessing the intervention's impact on child health, behavior, and development and caregiver stress and mental health.

Description:

Early-life trauma and related adversities are prevalent and associated with negative health, developmental, and behavioral outcomes in children. Research to design and test practical, scalable healthcare interventions that mitigate toxic stress is needed to promote improved health and developmental outcomes in children.

The Resilience Clinic is an interactive, caregiver-child psychoeducational intervention for parents and other adult caregivers of young children (ages 0-5 years) with exposure to traumatic events or other significant adversity. The aim of this primary-care based intervention is to prevent or mitigate the toxic stress response, thus promoting child resilience in the face of adversity, with the goal of improving child health, behavioral, and developmental outcomes.

The overall aim of this study is to evaluate the the efficacy and operational feasibility of the revised Resilience Clinic (RC). This is a non-randomized clinical trial comparing intervention caregiver-child dyads to a prospective control group drawn from a concurrent clinical trial (NCT05259436, The Collaborative Approach to Examining Adversity and Building Resilience Study (CARE), PI Thakur). In the intervention group, we will conduct pre-post intervention comparisons along with comparisons between the intervention group and the control group drawn from the CARE study. A subgroup analysis will compare two intervention arms (clinic based vs community-based intervention) to each other and the control condition. This clinical trial is supplemented by a mixed-methods quality improvement (QI) tools, including process measures (attendance and billing/claims data) to evaluate operational and financial feasibility; participant surveys/interviews/focus groups to assess acceptability; and analysis of quality improvement meeting notes.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: November 30, 2023
• Est. primary completion date: November 30, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 2 Years to 5 Years

Eligibility

Inclusion Criteria:

• Caregiver: 18 years old and older, primary caregiver, English or Spanish speaking

• Child: 2 to 5 years, PEARLS score > 1 or verbal disclosure of PEARLS adversity to primary care clinician/staff

Exclusion Criteria:

• Caregiver: active suicidality, other psychiatric issues

• Child: significant medical co-morbidities (i.e. disease requiring immunomodulators, chemo or radiation therapy, or hormonal therapy)

Related Conditions & MeSH terms

• Caregiver Stress
• Early Life Adversity

Intervention

Behavioral:
• Resilience Clinic
A psychoeducational caregiver-child intervention based in primary care, designed to mitigate toxic stress and promote child resilience. Participants engage in 6 weekly visits in primary care using an interactive curriculum based in the evidence-based Circle of Security Parenting along with mindfulness principles.
• Enhanced primary care
In addition to usual pediatric primary care, enhanced primary care (the control condition for this study) provides navigational services to link to community resources based on screening for unmet social needs (e.g., food insecurity, housing, financial strain).

Locations

Country	Name	City	State
United States	Asian Health Services	Oakland	California
United States	La Clinica de la Raza	Oakland	California
United States	UCSF Benioff Children's Hospital Oakland	Oakland	California
United States	UBCP-Bancroft Pediatrics	San Leandro	California

Sponsors (7)

Lead Sponsor	Collaborator
University of California, San Francisco	Asian Health Services, Kerry's Kids, La Clínica de La Raza Inc., Population Health Innovation Lab, UBCP Bancroft Pediatrics, UCSF Benioff Children's Hospital Oakland

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Parenting Stress Index Short Form (PSI) score	36-item caregiver-report questionnaire validated as a measure of parenting stress (level of stress within the context of parenting). Responses indicated on a 5-point Likert scale. Higher scores indicate higher levels of parenting stress.	baseline/enrollment and 2 week and 3-month follow-up after intervention ends
Primary	Change in Child Behavior Checklist (CBCL)-Preschool form total problems scale score	Caregiver-report questionnaire validated as a measure of child behavioral challenges; part of the Achenbach System of Empirically Based Assessment (ASEBA). The CBCL-Preschool form is validated for children ages 1.5-5 years based on behavior from the prior 2 months.	baseline/enrollment and 2 week and 3-month follow-up after intervention ends
Secondary	Change in Behavior Rating Inventory of Executive Function, Preschool Version (BRIEF-P) score	Caregiver-report questionnaire, validated as a measure of executive functioning in preschool aged children (ages 2-5:11)	baseline/enrollment and 2 week and 3-month follow-up after intervention ends
Secondary	Change in Patient-Reported Outcomes Measurement Information System (PROMIS) global health score	PROMIS is a set of person-centered measure evaluating the physical, mental, and social health of adults and children. This study uses the first question on the global scale, with a minimum value of 1 and maximum of 5; higher scores indicate better general health.	baseline/enrollment and 2 week and 3-month follow-up after intervention ends
Secondary	Change in Ages and Stages Questionnaire (ASQ)-3rd Edition scores	Caregiver-report questionnaire validated as a measure for risk of developmental delay in children ages 0-60 months.	baseline/enrollment to 3 month follow-up after intervention ends
Secondary	Change in Caregiver depression score on the Patient Health Questionnaire (PHQ)-8 scale	Questionnaire validated as a measure of depressive symptoms; higher scores indicate higher self-report depressive symptoms. Will be given to questionnaires to assess their depressive symptoms.	baseline/enrollment and 2 week and 3-month follow-up after intervention ends
Secondary	Change in Caregiver anxiety score on the Generalized Anxiety Disorder (GAD) scale	Questionnaire validated as a measure of anxiety symptoms; high scores indicate higher levels of anxiety. Will be given to caregivers to assess their anxiety symptoms.	baseline/enrollment and 2 week and 3-month follow-up after intervention ends
Secondary	Change in Perceived Stress Scale (PSS) total score- Caregiver general stress	Self-report questionnaire that measures global perceived stress based on feelings and thoughts during the last month. Higher scores indicate higher perceived stress. Will be given to caregivers as a measure of their general perceived stress.	baseline/enrollment and 2 week and 3-month follow-up after intervention ends
Secondary	Change in telomere length (children)	Telomere are nucleoproteins that protect the ends of chromosomes and can be used as a biomarker of cellular aging. Chronic stress has been associated with shorter telomere length. DNA will be extracted from cheek cells (obtained by buccal swab) in children.	baseline/enrollment to 3 month follow-up after intervention ends