A validation study of a modified Bouchard activity record that extends the concept of 'uptime' to Rett syndrome

QR Code

A validation study of a modified Bouchard activity record that extends the concept of 'uptime' to Rett syndrome

Aim - The aim of this study was to investigate the validity of using a Bouchard activity record (BAR) in individuals with Rett syndrome to measure physical activity, as compared with pragmatic criterion standard measures of walking status and step counts recorded using the StepWatch activity monitor...

Full description

Bibliographic Details
Main Authors:	Lor, L., Hill, Kylie, Jacoby, P., Leonard, H., Downs, Jennepher
Format:	Journal Article
Published:	Blackwell Publishing Ltd 2015
Online Access:	http://hdl.handle.net/20.500.11937/46404

Similar Items

Validating the Rett Syndrome Gross Motor Scale
by: Downs, Jennepher, et al.
Published: (2016)

Initial assessment of the StepWatch Activity Monitor™ to measure walking activity in Rett syndrome
by: Downs, Jennepher, et al.
Published: (2012)

The trajectories of sleep disturbances in Rett syndrome
by: Wong, K., et al.
Published: (2015)

Measurement of Sedentary Behaviors or "downtime" in Rett Syndrome
by: Stahlhut, M., et al.
Published: (2017)

From epidemiology to real world outcomes for the management of scoliosis in Rett syndrome
by: Downs, Jennepher, et al.
Published: (2016)

Quantification of walking-based physical activity and sedentary time in individuals with Rett syndrome
by: Downs, Jennepher, et al.
Published: (2017)

Rett syndrome: Establishing a novel outcome measure for walking activity in an era of clinical trials for rare disorders
by: Downs, Jennepher, et al.
Published: (2015)

Early Determinants of Fractures in Rett Syndrome
by: Downs, Jennepher, et al.
Published: (2008)

Quantitative and qualitative insights into the experiences of children with Rett syndrome and their families
by: Downs, Jennepher, et al.
Published: (2016)

Longitudinal hand function in Rett syndrome
by: Downs, Jennepher, et al.
Published: (2011)

Parental experiences of scoliosis management in Rett syndrome
by: Ager, S., et al.
Published: (2009)

Valproate and the risk of fracture in Rett syndrome
by: Leonard, H., et al.
Published: (2010)

Clinical and biological progress over 50 years in Rett syndrome
by: Leonard, H., et al.
Published: (2017)

The diagnostic odyssey to Rett Syndrome: The experience of an Australian family
by: Knott, M., et al.
Published: (2012)

Twenty years of surveillance in Rett syndrome: what does this tell us?
by: Anderson, A., et al.
Published: (2014)

A preliminary study on use of anticonvulsants and risk of fracture in Rett syndrome
by: Jian, Le, et al.
Published: (2007)

Early development and regression in Rett Syndrome
by: Lee, J.Y.L., et al.
Published: (2013)

Longitudinal bone mineral content and density in Rett syndrome and their contributing factors
by: Jefferson, Amanda, et al.
Published: (2015)

Building the repertoire of measures of walking in Rett syndrome
by: Stahlhut, M., et al.
Published: (2017)

Linking MECP2 and Pain Sensitivity : The Example of Rett Syndrome
by: Downs, Jennepher, et al.
Published: (2010)

Family satisfaction following spinal fusion in Rett syndrome
by: Downs, Jennepher, et al.
Published: (2016)

Parental perspectives on the communication abilities of their daughters with Rett syndrome.
by: Urbanowicz, A., et al.
Published: (2016)

Respiratory morbidity in Rett syndrome: an observational study
by: MacKay, J., et al.
Published: (2018)

A qualitative investigation of recovery after femoral fracture in Rett syndrome
by: Horne, T., et al.
Published: (2017)

Trends in diagnosis of Rett Syndrome in Australia
by: Fehr, S., et al.
Published: (2011)

Use of equipment and respite services and caregiver health among Australian families living with Rett syndrome
by: Urbanowicz, A., et al.
Published: (2011)

An exploration of the use of eye gaze and gestures in females with Rett syndrome
by: Urbanowicz, A., et al.
Published: (2016)

Determinants of quality of life in Rett syndrome: New findings on associations with genotype
by: Mendoza, J., et al.
Published: (2021)

Spinal fusion in girls with Rett syndrome: postoperative recovery and family experiences
by: Marr, C., et al.
Published: (2015)

The sibling experience: Living with Down syndrome or Rett syndrome in the family
by: Glasson, E., et al.
Published: (2016)

Perspectives on hand function in girls and women with Rett syndrome
by: Downs, Jennepher, et al.
Published: (2014)

Using a large international sample to investigate epilepsy in Rett syndrome
by: Bao, X., et al.
Published: (2013)

Atypical Presentations and Specific Genotypes Are Associated With a Delay in Diagnosis in Females With Rett Syndrome
by: Fehr, S., et al.
Published: (2010)

How can clinical ethics guide the management of comorbidities in the child with Rett syndrome?
by: Downs, Jennepher, et al.
Published: (2016)

Stereotypical hand movements in 144 subjects with Rett syndrome from the population-based Australian database
by: Carter, P., et al.
Published: (2010)

Experience of Gastrostomy Using a Quality Care Framework: The Example of Rett Syndrome
by: Downs, Jennepher, et al.
Published: (2014)

Gross Motor profile in Rett Syndrome as Determined by Video Analysis
by: Downs, Jennepher, et al.
Published: (2008)

Choice making in Rett syndrome: A descriptive study using video data
by: Urbanowicz, A., et al.
Published: (2016)

Altered Attainment of Developmental Milestones Influences the Age of Diagnosis of Rett Syndrome
by: Fehr, S., et al.
Published: (2011)

The Natural History of Scoliosis in Females with Rett Syndrome
by: Downs, Jennepher, et al.
Published: (2015)