A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical Trials

Author:

Raspa Melissa1,Bann Carla M.1,Gwaltney Angela1,Benke Timothy A.2,Fu Cary3,Glaze Daniel G.4,Haas Richard5,Heydemann Peter6,Jones Mary7,Kaufmann Walter E.8,Lieberman David9,Marsh Eric9,Peters Sarika10,Ryther Robin11,Standridge Shannon12,Skinner Steven A.13,Percy Alan K.14,Neul Jeffrey L.15

Affiliation:

1. Melissa Raspa, Carla M. Bann, and Angela Gwaltney, RTI International

2. Timothy A. Benke, University of Colorado School of Medicine

3. Cary Fu, Vanderbilt Kennedy Center

4. Daniel G. Glaze, Baylor College of Medicine

5. Richard Haas, University of California San Diego

6. Peter Heydemann, Rush University Medical Center

7. Mary Jones, Benioff Children's Hospital

8. Walter E. Kaufmann, Greenwood Genetic Center

9. David Lieberman and Eric Marsh, Children's Hospital Boston

10. Sarika Peters, Vanderbilt Kennedy Center

11. Robin Ryther, Washington University School of Medicine

12. Shannon Standridge, Cincinnati Children's Hospital

13. Steven A. Skinner, Greenwood Genetic Center

14. Alan K. Percy, University of Alabama at Birmingham

15. Jeffrey L. Neul, Vanderbilt Kennedy Center

Abstract

Abstract Rett syndrome (RTT) is a neurodevelopmental disorder that primarily affects females. Recent work indicates the potential for disease modifying therapies. However, there remains a need to develop outcome measures for use in clinical trials. Using data from a natural history study (n = 1,075), we examined the factor structure, internal consistency, and validity of the clinician-reported Motor Behavior Assessment scale (MBA). The analysis resulted in a five-factor model: (1) motor dysfunction, (2) functional skills, (3) social skills, (4) aberrant behavior, and (5) respiratory behaviors. Item Response Theory (IRT) analyses demonstrated that all items had acceptable discrimination. The revised MBA subscales showed a positive relationship with parent reported items, age, and a commonly used measure of clinical severity in RTT, and mutation type. Further work is needed to evaluate this measure longitudinally and to add items related to the RTT phenotype.

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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