The candidate is a Research Assistant Professor at the University of Florida. She has a professional degree in occupational therapy and a Ph.D. in Rehabilitation Science. Her long- term goal is to become firmly established as an independent investigator designing clinical studies that examine the relationships between activity, participation and quality of life (QoL) with pathophysiology, muscle strength and functional ability in children with chronic illnesses and disability. The candidate will primarily be mentored by Dr. Krista Vandenborne, with Dr. Barbara Curbow serving as secondary mentor. Each mentor, as well as the candidate's advisory committee, will help her transition from junior faculty member to an independent investigator through a combination of activities including: didactic coursework, mentored laboratory and internal/external training experiences, one-on-one meetings with mentors, attendance at seminars and conferences, execution of the research plan and manuscript preparation and grant writing. Four national experts were selected to serve on the mentoring advisory committee in order to provide the breadth of content expertise necessary for carrying out the career development and research plans. A very important component of the career development plan includes training at the National Institutes of Health for a three-month period in both year 1 and year 2 in the lab of Dr. Kenneth H. Fischbeck, Senior Investigator, Division of Intramural Research at NINDS, as well as the lab of Dr. Eric Hoffman, Research Center for Genetic Medicine, Children's National Medical Center (CNMC). The University of Florida has a strong commitment to rehabilitation research and is committed to supporting the candidate through the course of this mentored award.
The specific aims of this research proposal are to: 1) Evaluate activity, participation, quality of life, pathophysiology, muscle strength, and functional ability in boys with Duchenne Muscular Dystrophy (DMD) compared to healthy age-matched boys;2) Determine the relationships between activity, participation and quality of life with quantitative MR measures of muscle and disease severity (strength and functional ability) in boys with DMD compared to healthy age-matched boys;3) Evaluate disease progression in boys with DMD using a longitudinal study design for measures of physical activity, participation, quality of life, pathophysiology, muscle strength and functional ability;and 4) Explore environmental and parental perceptions, attributes and behaviors that facilitate and/or inhibit levels of activity, participation, muscle strength, functional ability and quality of life in boys with DMD. Thirty ambulatory boys with DMD and 10 age- matched controls will be enrolled and physical activity, participation in daily life activities, quality of life, muscle pathology, strength and functional ability will be quantified and relationships determined between the variables and changes that occur over time. This study is designed to investigate the impact of muscle dysfunction and impaired functional ability on participation and quality of life in boys with DMD and to serve as a future guide for evaluating intervention effectiveness through comprehensive measurement of disease progression. Moreover, information from these studies will provide important clinical implications to target therapeutic interventions for children and families.
Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy and is characterized by progressive muscle damage and a loss of muscle function in male children. Traditionally, clinical and intervention studies in DMD have focused on physiological and functional measures that are affected by the disease, but fail to explore how the disease impacts a child's participation or provide important information about """"""""real world"""""""" abilities. This project stresses the importance of integrating both quantitative biological and functional measures of disease progression and assessments of activity, participation and QoL into future clinical studies and trials to determine the effectiveness of new therapies and interventions being developed for DMD.
|Bendixen, Roxanna M; Butrum, Jocelyn; Jain, Mina S et al. (2017) Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy. Neuromuscul Disord 27:278-285|
|Bendixen, Roxanna M; Houtrow, Amy (2016) Parental Reflections on the Diagnostic Process for Duchenne Muscular Dystrophy: A Qualitative Study. J Pediatr Health Care :|
|Kreider, Consuelo M; Bendixen, Roxanna M; Young, Mary Ellen et al. (2016) Social networks and participation with others for youth with learning, attention, and autism spectrum disorders. Can J Occup Ther 83:14-26|
|Reynolds, Stacey; Kreider, Consuelo M; Meeley, Lauren E et al. (2015) Taste perception and sensory sensitivity: Relationship to feeding problems in boys with Barth Syndrome. J Rare Disord 3:1-9|
|Kreider, Consuelo M; Bendixen, Roxanna M; Mann, William C et al. (2015) Mixed-Method Exploration of Social Network Links to Participation. OTJR (Thorofare N J) 35:151-9|
|Kreider, Consuelo M; Bendixen, Roxanna M; Lutz, Barbara J (2015) Holistic Needs of University Students with Invisible Disabilities: A Qualitative Study. Phys Occup Ther Pediatr 35:426-41|
|Kreider, Consuelo M; Bendixen, Roxanna M; Huang, Yu Yun et al. (2014) Review of occupational therapy intervention research in the practice area of children and youth 2009-2013. Am J Occup Ther 68:e61-73|
|Lim, Yoonjeong; Velozo, Craig; Bendixen, Roxanna M (2014) The level of agreement between child self-reports and parent proxy-reports of health-related quality of life in boys with Duchenne muscular dystrophy. Qual Life Res 23:1945-52|
|Bendixen, Roxanna M; Lott, Donovan J; Senesac, Claudia et al. (2014) Participation in daily life activities and its relationship to strength and functional measures in boys with Duchenne muscular dystrophy. Disabil Rehabil 36:1918-23|
|Reynolds, Stacey; Kreider, Consuelo M; Bendixen, Roxanna (2012) A mixed-methods investigation of sensory response patterns in Barth syndrome: a clinical phenotype? Am J Med Genet A 158A:1647-53|
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