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NCT07048574Recruiting

TIDES 2.0: Prevalence and Longitudinal Course of Depression, Anxiety, and Behavior Problems in Children With Cystic Fibrosis Under 12 Years of Age

State University of New York at Buffalo

Start Date

6/2/2025

Completion Date

6/30/2028

Summary

This is a longitudinal, observational epidemiological study designed to estimate the prevalence of depression, anxiety, and behavior problems in children ages 18 months through 11 years with cystic fibrosis (CF).

Detailed Description

Integration of mental health (MH) screening and treatment into cystic fibrosis (CF) care represents over 10 years of research and clinical progress, driven by elevated rates of depression and anxiety in the International Depression Epidemiological Study, MH guidelines, and CF Foundation implementation support to screen adolescents and adults in all CF Centers. Benefits of screening include earlier identification, greater access to care, reduced stigma, and positive uptake from the CF community. However, TIDES did not include children with CF under 12 years. Depression and anxiety have increased dramatically in young children, with new guidelines for MH screening of children in primary care. Given the pediatric MH crisis and the widespread adoption of cystic fibrosis fibrosis transmembrane conductance regulator (CFTR) modulator therapy, which have been associated with adverse events, there is an urgent need to gather MH data in children with CF \<12 years. Thus, the goals of this study are to evaluate the national, longitudinal prevalence of depression, anxiety, and behavior problems in children with CF 18 months through 11 years, evaluate and compare the performance of two widely used brief screeners (criterion validity, sensitivity, specificity) to identify the optimal measures for this population, and characterize neuropsychiatric adverse events (AEs) associated with CFTR modulator therapy in this age group. Purposive randomized sampling will be used to recruit 600 children (half 18 mos.-5 yrs. and half 6-11 yrs.) at 16 CF Centers across the US. This study will estimate the prevalence of children above the clinical cut-score on each symptom domain (depression, anxiety, behavior problems) and evaluate their longitudinal course and predictors. Rigorous mixed methods will be used to describe any potential AEs perceived by parents or children to be associated with CFTR modulator therapy. This study will provide the groundwork to extend mental health screening and care to younger children with CF.

Eligibility Criteria

Age Range: No minimum to 11 years

Inclusion Criteria: 1. Child with a diagnosis of Cystic fibrosis (CF) actively followed by the CF care team at a participating site 2. Child is age 18 months thru 11 years 3. English and/or Spanish speaking 4. Parent/legal guardian willing and able to give informed consent, and for minor participants ages 7 thru 11 years able to give assent. Exclusion Criteria: * Unable or unwilling to participate in study procedures, or at Site PI discretion.

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Conditions

Cystic Fibrosis (CF)

Locations

Children's Hospital of Orange County

Orange, California 92868

United States

Children's Hospital Colorado

Aurora, Colorado 80045

United States

Joe DiMaggio

Hollywood, Florida 33021

United States

Nemours Foundation

Orlando, Florida 32827

United States

Indiana University

Bloomington, Indiana 47405

United States

Massachusetts General Hospital

Boston, Massachusetts 02114

United States

University at Buffalo

Buffalo, New York 14215

United States

University of North Carolina School of Medicine

Chapel Hill, North Carolina 27599

United States

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio 45229

United States

Brown University Health

Providence, Rhode Island 02903

United States

UT Southwestern

Plano, Texas 75235

United States

Children's Hospital of Richmond at Virginia Commonwealth University

Richmond, Virginia 23219

United States

Seattle Children's Hospital

Seattle, Washington 98105

United States