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Articles

Coaching in context: parent perspectives

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Pages 16-30 | Received 02 Jul 2021, Accepted 12 Nov 2021, Published online: 02 Dec 2021

References

  • Blanes, L., Carmagnani, M. I. S., & Ferreira, L. M. (2007). Health-related quality of life of primary caregivers of persons with paraplegia. Spinal Cord, 45(6), 399–403. https://doi.org/10.1038/sj.sc.3102038
  • Boschen, K. A., Tonack, M., & Gargaro, J. (2010). The impact of being a support provider to a person living in the community with a spinal cord injury. Rehabilitation Psychology, 50(4), 397–407. https://doi.org/10.1037/0090-5550.50.4.397
  • Bourke-Taylor, H., Howie, L., & Law, M. (2010). Impact of caring for a school-aged child with a disability: Understanding mothers’ perspectives. Australian Occupational Therapy Journal, 57(2), 127–136. https://doi.org/10.1111/j.1440-1630.2009.00817.x
  • Cadematori, C., Alpajora, B., Sivori, T., Betz, S., Gerhardt, N., Dunn, W., & Mulcahey, M. (2021). Preliminary examination of coaching in context with clients with spinal cord injury. Spinal Cord Series and Cases, 7, 27. https://doi.org/10.1038/s41394-021-00391-9
  • Dalvand, H., Hosseini, S. A., Rassafiani, M., Samadi, S. A., Khankeh, H. R., & Kelly, G. (2015). Co-occupations: The caregiving challenges of mothers of children with cerebral palsy. British Journal of Occupational Therapy, 78(7), 450–459. https://doi.org/10.1177/0308022614562793
  • Foster, L., Dunn, W., & Lawson, L. M. (2013). Coaching mothers of children with autism: A qualitative study for occupational therapy practice. Physical & Occupational Therapy in Pediatrics, 33(2), 253–263. https://doi.org/10.3109/01942638.2012.747581
  • Gajraj-Singh, P. (2011). Psychological impact and the burden of caregiving for persons with spinal cord injury (SCI) living in the community in Fiji. Spinal Cord, 49(8), 928–934. https://doi.org/10.1038/sc.2011.15
  • Gorzkowski, J., Kelly, E. H., Klaas, S. J., & Vogel, L. C. (2011). Obstacles to community participation among youth with spinal cord injury. The Journal of Spinal Cord Medicine, 34(6), 576–585. https://doi.org/10.1179/2045772311Y.0000000037
  • Graham, F., Rodger, S., & Ziviani, J. (2009). Coaching parents to enable children’s participation: An approach for working with parents and their children. Australian Occupational Therapy Journal, 56(1), 16–23. https://doi.org/10.1111/j.1440-1630.2008.00736.x
  • Graham, F., Rodger, S., & Ziviani, J. (2010). Enabling occupational performance of children through coaching parents: Three case reports. Physical and Occupational Therapy in Pediatrics, 30(1), 4–15. https://doi.org/10.3109/01942630903337536
  • Green, S. E. (2007). ‘We’re tired, not sad’: Benefits and burdens of mothering a child with a disability. Social Science and Medicine, 64(1), 150–163. https://doi.org/10.1016/j.socscimed.2006.08.025
  • Holmbeck, G., Greenley, R. N., Coakley, R. M., Greco, J., & Hagstrom, J. (2006). Family functioning in children and adolescents with spina bifida: An evidence-based review of research and interventions. Journal of Developmental Behavioral Pediatrics, 27(3), 249–277. https://doi.org/10.1097/00004703-200606000-00012
  • House, L. A., Russell, H. F., Kelly, E. H., Gerson, A., & Vogel, L. C. (2009). Rehabilitation and future participation of youth following spinal cord injury: Caregiver perspectives. Spinal Cord, 47(12), 882–886. https://doi.org/10.1038/sc.2009.64
  • Kelly, E. H., Anderson, C. J., Garma, S. I., Russell, H. F., Klaas, S. J., Gorzkwoski, J. A., & Vogel, L. C. (2011). Relationships between the psychological characteristics of youth with spinal cord injury and their primary caregivers. Spinal Cord, 49(2), 200–205. https://doi.org/10.1038/sc.2010.78
  • Kelly, E. H., Mulcahey, M. J., Klaas, S., Russell, H. F., Anderson, C. J., & Vogel, L. C. (2012). Psychosocial outcomes among youth with spinal cord injury and their primary caregivers. Topics in Spinal Cord Injury Rehabilitation, 18(1), 67–72. https://doi.org/10.1310/sci1801-67
  • Kelly, E. H., Riordan, A. L., Zebracki, K., Thorpe, S., & Vogel, L. C. (2016). Relationships between caregiver characteristics and health-related quality of life among youth with spinal cord injury. Topics in Spinal Cord Injury Rehabilitation, 22(2), 149–157. https://doi.org/10.1310/sci2016-00012
  • McDonald, C. M., Haberman, D., & Brown, N. (2013). Self-efficacy: Empowering parents of children with cystic fibrosis. Journal of Cystoc Fibrosis, 12(5), 538–543. https://doi.org/10.1016/j.jcf.2012.11.014
  • Miller, W., & Rollnick, S. (2013). Motivational interviewing: Helping people change behavior. Guilford Press.
  • Nelson, A. (2002). A metasynthesis: Mothering other than normal children. Qualitative Health Research, 12(4), 515–530. https://doi.org/10.1177/104973202129120043
  • Nicolais, C. J., Perrin, P. B., Panyavin, I., Nicholls, E. G., Leonor, S., Plaza, O., Quintero, L. M., & Arango-Lasprilla, J. C. (2016). Family dynamics and psychosocial functioning in children with SCI/D from Colombia, South America. Journal of Spinal Cord Medicine, 39(1), 58–65. https://doi.org/10.1179/2045772314Y.0000000291
  • Post, M. W. M., Bloemen, J., & de Witte, L. P. (2005). Burden of support for partners of persons with spinal cord injuries. Spinal Cord, 43(5), 311–319. https://doi.org/10.1038/sj.sc.3101704
  • Potvin, M. C., Prelock, P. A., & Savard, L. (2018). Supporting children with autism and their families: A culturally-responsive family driven interprofessional process. Pediatric Clinics of North America, 65(1), 47–57. https://doi.org/10.1016/j.pcl.2017.08.020
  • Raj, J. T., Manigandan, C., & Jacob, K. S. (2006). Leisure satisfaction and psychiatric morbidity among informal carers of people with spinal cord injury. Spinal Cord, 44, 676–679.
  • Seligman, M. E. P., & Csikszentmihalyi, M. (2014). Positive psychology: An introduction. American Psychologist, 55(1), 5–14. https://doi.org/10.1007/978-94-017-9088-8_18
  • Tsay, S. L., & Hung, L. O. (2004). Empowerment of patients with end-stage renal disease – A randomized controlled trial. International Journal of Nursing Studies, 41(1), 59–65. https://doi.org/10.1016/s0020-7489(03)00095-6
  • Unalan, H., Gencosmanoglu, B., Akgun, K., Karamehmetoglu, S., Tuna, H., Ones, K., Rahimpenah, A., Uzun, E., & Tuzun, F. (2001). Quality of life of primary caregivers of spinal cord injury survivors living in the community: Controlled study with short form-36 questionnaire. Spinal Cord, 39(6), 318–322. https://doi.org/10.1038/sj.sc.3101163
  • Vermaes, I., Janssens, J., Bosman, A., & Gerris, J. (2005). Parents’ psychological adjustment in families of children with Spina Bifida: A metaanalysis. BMC Pediatrics, 5(1), 32. https://doi.org/10.1186/1471-2431-5-32

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