Attendance at Fragile X Specialty Clinics: Facilitators and Barriers

Author:

Kidd Sharon A.1,Raspa Melissa2,Clark Renée3,Usrey-Roos Holly4,Wheeler Anne C.5,Liu Jessica A.6,Wylie Amanda7,Sherman Stephanie L.8

Affiliation:

1. Sharon A. Kidd, University of California, San Francisco;

2. Melissa Raspa, RTI International;

3. Renée Clark, University of North Carolina, Chapel Hill;

4. Holly Usrey-Roos, National Fragile X Foundation, Washington, DC;

5. Anne C. Wheeler, RTI International;

6. Jessica A. Liu, Sutter Health, Walnut Creek, CA;

7. Amanda Wylie, RTI International;

8. Stephanie L. Sherman, Emory University.

Abstract

Abstract The objectives were to describe the demographic characteristics of children with Fragile X syndrome (FXS) and to determine predictors of attendance at Fragile X (FX) clinics. Findings from the Community Support Network (CSN) and Our Fragile X World (OFXW) samples showed that children who attended FX Clinics were mostly male, high-school aged or younger, and white, non-Hispanic. Using logistic regression models, awareness about FX Clinic services, guardian education, and income (CSN), and child age, family income, and total number of co-occurring conditions (OFXW) were predictors of clinic attendance. Demographic and child characteristics accounted for a large portion of the explained variance. Importantly, symptom severity and parent knowledge about services were independent predictors beyond the demographic characteristics of families.

Publisher

American Association on Intellectual and Developmental Disabilities (AAIDD)

Subject

Psychiatry and Mental health,Neurology (clinical),Arts and Humanities (miscellaneous),Developmental and Educational Psychology,Neuropsychology and Physiological Psychology,General Medicine,Pediatrics, Perinatology and Child Health

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