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Yıl 2023, Cilt: 6 Sayı: 2, 218 - 224, 27.06.2023
https://doi.org/10.33438/ijdshs.1265907

Öz

Kaynakça

  • Barutcu, A., Barutcu, S., Kolkiran, S., & Ozdener, F. (2021). Evaluation of anxiety, depression and burden on caregivers of children with cerebral palsy. Developmental neurorehabilitation, 24(8), 555-560.
  • Bourke‐Taylor, H., Howie, L., Law, M., & Pallant, J. F. (2012). Self‐reported mental health of mothers with a school‐aged child with a disability in Victoria: A mixed method study. Journal of paediatrics and child health, 48(2), 153-159.
  • Bumin, G., Günal, A., & Tükel, Ş. (2008). Anxiety, depression and quality of life in mothers of disabled children. Journal of SDU Faculty of Medicine, 15(1), 6-11.
  • Byrne, M. B., Hurley, D. A., Daly, L., & Cunningham, C. G. (2010). Health status of caregivers of children with cerebral palsy. Child: care, health and development, 36(5), 696-702.
  • Caicedo, C. (2014). Families with special needs children: family health, functioning, and care burden. Journal of the American Psychiatric Nurses Association, 20(6), 398-407.
  • Cangür, Ş., Civan, G., Çoban, S., Mazhar, K. O. Ç., Karakoç, H., Budak, S., ... & Ankaralı, H. (2013). Comparative evaluation of the participation of families with physically and/or mentally handicapped individuals in social life in Düzce. Duzce University Journal of Health Sciences Institute 3(3), 1-9.
  • Coller, R. J., Berry, J. G., Kuo, D. Z., Kuhlthau, K., Chung, P. J., Perrin, J. M., Hoover, C. G., Warner, G., Shelton, C., Thompson, L. R., Garrity, B., & Stille, C. J. (2020). Health system research priorities for children and youth with special health care needs. Pediatrics (Evanston), 145(3)
  • Dehghan, L., Dalvand, H., Feizi, A., Samadi, S. A., & Hosseini, S. A. (2016). Quality of life in mothers of children with cerebral palsy: The role of children’s gross motor function. Journal of child health care, 20(1), 17-26.
  • Erkin, G., Elhan, A. H., Aybay, C., Sirzai, H., & Ozel, S. (2007). Validity and reliability of the turkish translation of the pediatric evaluation of disability inventory (PEDI). Disability and Rehabilitation, 29(16), 1271-1279.
  • Farajzadeh, A., Maroufizadeh, S., & Amini, M. (2020). Factors associated with quality of life among mothers of children with cerebral palsy. International journal of nursing practice, 26(3), e12811.
  • Gençer Özkan, C. (2020). The validity and reliability of the adult carer quality of life questionnaire in caregivers of chronically disabled children (Master's thesis, Institute of Health Sciences).
  • Gulati, S., & Sondhi, V. (2018). Cerebral Palsy: An Overview. In Indian Journal of Pediatrics (Vol. 85, Issue 11, pp. 1006–1016). Springer.
  • Haimour, A. I., & Abu-Hawwash, R. M. (2012). Evaluating quality of life of parents having a child with disability. International Interdisciplinary Journal of Education, 1(2), 37-43.
  • Haley, S. M., Coster, W. I., Kao, Y., Dumas, H. M., Fragala-Pinkham, M. A., Kramer, J. M., Ludlow, L. H., & Moed, R. (2010). Lessons from use of the pediatric evaluation of disability inventory: Where do we go from here? Pediatric Physical Therapy, 22(1), 69-75.
  • Hastings, R. P. (2003). Child behaviour problems and partner mental health as correlates of stress in mothers and fathers of children with autism. Journal of Intellectual Disability Research, 47(4-5), 231-237.
  • Isa, S. N. I., Aziz, A. A., Ab Rahman, A., Ibrahim, M. I., Ibrahim, W. P. W., Mohamad, N., ... & Van Rostenberghe, H. (2013). The impact of children with disabilities on parent health-related quality of life and family functioning in Kelantan and its associated factors. Journal of Developmental & Behavioral Pediatrics, 34(4), 262-268.
  • Joseph, S., Becker, S., Elwick, H., & Silburn, R. (2012). Adult carers quality of life questionnaire ACQoL development of an evidencebased tool. Mental Health Review Journal, 17(2), 57-69.
  • Lindley, L. C., & Mark, B. A. (2010). Children with special health care needs: Impact of health care expenditures on family financial burden. Journal of child and family studies, 19, 79-89.
  • Li-Tsang, C. W. P., Yau, M. K. S., & Yuen, H. K. (2001). Success in parenting children with developmental disabilities: Some characteristics, attitudes and adaptive coping skills. The British Journal of Development Disabilities, 47(93), 61-71.
  • Ones, K., Yilmaz, E., Cetinkaya, B., & Caglar, N. (2005). Assessment of the quality of life of mothers of children with cerebral palsy (primary caregivers). Neurorehabilitation and Neural Repair, 19(3), 232-237.
  • Schulz, R., & Sherwood, P. R. (2008). Physical and mental health effects of family caregiving. Journal of Social Work Education, 44(sup3), 105-113.
  • Sen, E., & Yurtsever, S. (2007). Difficulties experienced by families with disabled children. Journal for Specialists in Pediatric Nursing, 12(4), 238-252.
  • Sertel, M., Şimşek, T. T., Yümin, E. T., & Bayraktaroğlu, F. (2016). Investigation of the relationship between body image, depression level and life satisfaction in mothers with chronically disabled children. Journal of Social Policy Studies, (37), 33-50.
  • Shirai, Y., Silverberg Koerner, S., & Baete Kenyon, D. (2009). Reaping caregiver feelings of gain: The roles of socio-emotional support and mastery. Aging and Mental Health, 13(1), 106-117.
  • Sonune, S. P., Gaur, A. K., & Shenoy, A. (2021). Prevalence of depression and quality of life in primary caregiver of children with cerebral palsy. Journal of family medicine and primary care, 10(11), 4205.
  • Stevenson, R. D., Conaway, M., Chumlea, W. C., Rosenbaum, P., Fung, E. B., Henderson, R. C., Worley, G., Liptak, G., O'Donnell, M., Samson-Fang, L., Stallings, V. A., NAGCP Study, & North American Growth in Cerebral Palsy Study. (2006). Growth and health in children with moderate-to-severe cerebral palsy. Pediatrics (Evanston), 118(3), 1010-1018.
  • Tekinarslan, I. C. (2013). A comparison study of depression and quality of life in Turkish mothers of children with Down syndrome, cerebral palsy, and autism spectrum disorder. Psychological Reports, 112(1), 266-287.
  • Yılmaz, O., Yıldırım, S. A., Öksüz, C., Atay, S., & Turan, E. (2010). Mothers' depression and health‐related quality of life in neuromuscular diseases: role of functional independence level of the children. Pediatrics International, 52(4), 648-652.
  • Yilmaz, H., Erkin, G., & Nalbant, L. (2013). Depression and anxiety levels in mothers of children with cerebral palsy: A controlled study. European Journal of Physical and Rehabilitation Medicine, 49(6), 823-827.

The Investigation of Relationship between Functional Mobility Levels of Children with Chronic Disability and Caregivers’ Quality of Life

Yıl 2023, Cilt: 6 Sayı: 2, 218 - 224, 27.06.2023
https://doi.org/10.33438/ijdshs.1265907

Öz

Purpose: This study aims to look at the relationship between carers' quality of life and the functional mobility levels of children with chronic disabilities.Methods: The study included 30 children (22 boys, 8 girls) with chronic disabilities and their caregivers. The socio-demographic characteristics of the children and caregivers were collected.Caregivers' quality of life was evaluated with the Adult Carer Quality of Life Questionnaire (AC-QoL), and children’s functional mobility was evaluated with the mobility subscale of the Pediatric Evaluation Of Disability Inventory (PEDI-Mobility). Results: The age of the children included in the study was 7.0 (5.0-12.0) years and the age of their caregivers was 38.00 (32.75-41.25) years. The AC-QoL score of caregivers was 85.00 (72.00-93.50) out of a total of 120 points, and the PEDI-Mobility score was 33.00 (3.75-53.00) out of a total of 58 points. In the correlation analysis, no significant correlation was found between the PEDI-Mobility total score and the AC-QoL total score (p>0.05).However, there was a negative correlation between the PEDI-Mobility total score and the AC-QoL “ability to care” subscale score(r= -0.403; p=0.027). Conclusion: According to the results of the study, no relationship was found between the functional levels of children and the quality of life of their caregivers. Studies with a larger sample size and consideration of aspects including sociocultural level, economic considerations, and health services that may affect the quality of life of families are regarded to be necessary in order to achieve more conclusive findings on this subject.

Kaynakça

  • Barutcu, A., Barutcu, S., Kolkiran, S., & Ozdener, F. (2021). Evaluation of anxiety, depression and burden on caregivers of children with cerebral palsy. Developmental neurorehabilitation, 24(8), 555-560.
  • Bourke‐Taylor, H., Howie, L., Law, M., & Pallant, J. F. (2012). Self‐reported mental health of mothers with a school‐aged child with a disability in Victoria: A mixed method study. Journal of paediatrics and child health, 48(2), 153-159.
  • Bumin, G., Günal, A., & Tükel, Ş. (2008). Anxiety, depression and quality of life in mothers of disabled children. Journal of SDU Faculty of Medicine, 15(1), 6-11.
  • Byrne, M. B., Hurley, D. A., Daly, L., & Cunningham, C. G. (2010). Health status of caregivers of children with cerebral palsy. Child: care, health and development, 36(5), 696-702.
  • Caicedo, C. (2014). Families with special needs children: family health, functioning, and care burden. Journal of the American Psychiatric Nurses Association, 20(6), 398-407.
  • Cangür, Ş., Civan, G., Çoban, S., Mazhar, K. O. Ç., Karakoç, H., Budak, S., ... & Ankaralı, H. (2013). Comparative evaluation of the participation of families with physically and/or mentally handicapped individuals in social life in Düzce. Duzce University Journal of Health Sciences Institute 3(3), 1-9.
  • Coller, R. J., Berry, J. G., Kuo, D. Z., Kuhlthau, K., Chung, P. J., Perrin, J. M., Hoover, C. G., Warner, G., Shelton, C., Thompson, L. R., Garrity, B., & Stille, C. J. (2020). Health system research priorities for children and youth with special health care needs. Pediatrics (Evanston), 145(3)
  • Dehghan, L., Dalvand, H., Feizi, A., Samadi, S. A., & Hosseini, S. A. (2016). Quality of life in mothers of children with cerebral palsy: The role of children’s gross motor function. Journal of child health care, 20(1), 17-26.
  • Erkin, G., Elhan, A. H., Aybay, C., Sirzai, H., & Ozel, S. (2007). Validity and reliability of the turkish translation of the pediatric evaluation of disability inventory (PEDI). Disability and Rehabilitation, 29(16), 1271-1279.
  • Farajzadeh, A., Maroufizadeh, S., & Amini, M. (2020). Factors associated with quality of life among mothers of children with cerebral palsy. International journal of nursing practice, 26(3), e12811.
  • Gençer Özkan, C. (2020). The validity and reliability of the adult carer quality of life questionnaire in caregivers of chronically disabled children (Master's thesis, Institute of Health Sciences).
  • Gulati, S., & Sondhi, V. (2018). Cerebral Palsy: An Overview. In Indian Journal of Pediatrics (Vol. 85, Issue 11, pp. 1006–1016). Springer.
  • Haimour, A. I., & Abu-Hawwash, R. M. (2012). Evaluating quality of life of parents having a child with disability. International Interdisciplinary Journal of Education, 1(2), 37-43.
  • Haley, S. M., Coster, W. I., Kao, Y., Dumas, H. M., Fragala-Pinkham, M. A., Kramer, J. M., Ludlow, L. H., & Moed, R. (2010). Lessons from use of the pediatric evaluation of disability inventory: Where do we go from here? Pediatric Physical Therapy, 22(1), 69-75.
  • Hastings, R. P. (2003). Child behaviour problems and partner mental health as correlates of stress in mothers and fathers of children with autism. Journal of Intellectual Disability Research, 47(4-5), 231-237.
  • Isa, S. N. I., Aziz, A. A., Ab Rahman, A., Ibrahim, M. I., Ibrahim, W. P. W., Mohamad, N., ... & Van Rostenberghe, H. (2013). The impact of children with disabilities on parent health-related quality of life and family functioning in Kelantan and its associated factors. Journal of Developmental & Behavioral Pediatrics, 34(4), 262-268.
  • Joseph, S., Becker, S., Elwick, H., & Silburn, R. (2012). Adult carers quality of life questionnaire ACQoL development of an evidencebased tool. Mental Health Review Journal, 17(2), 57-69.
  • Lindley, L. C., & Mark, B. A. (2010). Children with special health care needs: Impact of health care expenditures on family financial burden. Journal of child and family studies, 19, 79-89.
  • Li-Tsang, C. W. P., Yau, M. K. S., & Yuen, H. K. (2001). Success in parenting children with developmental disabilities: Some characteristics, attitudes and adaptive coping skills. The British Journal of Development Disabilities, 47(93), 61-71.
  • Ones, K., Yilmaz, E., Cetinkaya, B., & Caglar, N. (2005). Assessment of the quality of life of mothers of children with cerebral palsy (primary caregivers). Neurorehabilitation and Neural Repair, 19(3), 232-237.
  • Schulz, R., & Sherwood, P. R. (2008). Physical and mental health effects of family caregiving. Journal of Social Work Education, 44(sup3), 105-113.
  • Sen, E., & Yurtsever, S. (2007). Difficulties experienced by families with disabled children. Journal for Specialists in Pediatric Nursing, 12(4), 238-252.
  • Sertel, M., Şimşek, T. T., Yümin, E. T., & Bayraktaroğlu, F. (2016). Investigation of the relationship between body image, depression level and life satisfaction in mothers with chronically disabled children. Journal of Social Policy Studies, (37), 33-50.
  • Shirai, Y., Silverberg Koerner, S., & Baete Kenyon, D. (2009). Reaping caregiver feelings of gain: The roles of socio-emotional support and mastery. Aging and Mental Health, 13(1), 106-117.
  • Sonune, S. P., Gaur, A. K., & Shenoy, A. (2021). Prevalence of depression and quality of life in primary caregiver of children with cerebral palsy. Journal of family medicine and primary care, 10(11), 4205.
  • Stevenson, R. D., Conaway, M., Chumlea, W. C., Rosenbaum, P., Fung, E. B., Henderson, R. C., Worley, G., Liptak, G., O'Donnell, M., Samson-Fang, L., Stallings, V. A., NAGCP Study, & North American Growth in Cerebral Palsy Study. (2006). Growth and health in children with moderate-to-severe cerebral palsy. Pediatrics (Evanston), 118(3), 1010-1018.
  • Tekinarslan, I. C. (2013). A comparison study of depression and quality of life in Turkish mothers of children with Down syndrome, cerebral palsy, and autism spectrum disorder. Psychological Reports, 112(1), 266-287.
  • Yılmaz, O., Yıldırım, S. A., Öksüz, C., Atay, S., & Turan, E. (2010). Mothers' depression and health‐related quality of life in neuromuscular diseases: role of functional independence level of the children. Pediatrics International, 52(4), 648-652.
  • Yilmaz, H., Erkin, G., & Nalbant, L. (2013). Depression and anxiety levels in mothers of children with cerebral palsy: A controlled study. European Journal of Physical and Rehabilitation Medicine, 49(6), 823-827.
Toplam 29 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Engelliler için Beden Eğitimi, Spor ve Fiziksel Aktivite
Bölüm Original Article
Yazarlar

Ramil Ahmadov 0000-0003-3811-9229

Nazlı Demir 0000-0003-1057-2814

Merve Kurt 0000-0002-8353-1338

Tülay Tarsuslu 0000-0003-3797-8857

Erken Görünüm Tarihi 6 Haziran 2023
Yayımlanma Tarihi 27 Haziran 2023
Yayımlandığı Sayı Yıl 2023 Cilt: 6 Sayı: 2

Kaynak Göster

APA Ahmadov, R., Demir, N., Kurt, M., Tarsuslu, T. (2023). The Investigation of Relationship between Functional Mobility Levels of Children with Chronic Disability and Caregivers’ Quality of Life. International Journal of Disabilities Sports and Health Sciences, 6(2), 218-224. https://doi.org/10.33438/ijdshs.1265907
AMA Ahmadov R, Demir N, Kurt M, Tarsuslu T. The Investigation of Relationship between Functional Mobility Levels of Children with Chronic Disability and Caregivers’ Quality of Life. International Journal of Disabilities Sports and Health Sciences. Haziran 2023;6(2):218-224. doi:10.33438/ijdshs.1265907
Chicago Ahmadov, Ramil, Nazlı Demir, Merve Kurt, ve Tülay Tarsuslu. “The Investigation of Relationship Between Functional Mobility Levels of Children With Chronic Disability and Caregivers’ Quality of Life”. International Journal of Disabilities Sports and Health Sciences 6, sy. 2 (Haziran 2023): 218-24. https://doi.org/10.33438/ijdshs.1265907.
EndNote Ahmadov R, Demir N, Kurt M, Tarsuslu T (01 Haziran 2023) The Investigation of Relationship between Functional Mobility Levels of Children with Chronic Disability and Caregivers’ Quality of Life. International Journal of Disabilities Sports and Health Sciences 6 2 218–224.
IEEE R. Ahmadov, N. Demir, M. Kurt, ve T. Tarsuslu, “The Investigation of Relationship between Functional Mobility Levels of Children with Chronic Disability and Caregivers’ Quality of Life”, International Journal of Disabilities Sports and Health Sciences, c. 6, sy. 2, ss. 218–224, 2023, doi: 10.33438/ijdshs.1265907.
ISNAD Ahmadov, Ramil vd. “The Investigation of Relationship Between Functional Mobility Levels of Children With Chronic Disability and Caregivers’ Quality of Life”. International Journal of Disabilities Sports and Health Sciences 6/2 (Haziran 2023), 218-224. https://doi.org/10.33438/ijdshs.1265907.
JAMA Ahmadov R, Demir N, Kurt M, Tarsuslu T. The Investigation of Relationship between Functional Mobility Levels of Children with Chronic Disability and Caregivers’ Quality of Life. International Journal of Disabilities Sports and Health Sciences. 2023;6:218–224.
MLA Ahmadov, Ramil vd. “The Investigation of Relationship Between Functional Mobility Levels of Children With Chronic Disability and Caregivers’ Quality of Life”. International Journal of Disabilities Sports and Health Sciences, c. 6, sy. 2, 2023, ss. 218-24, doi:10.33438/ijdshs.1265907.
Vancouver Ahmadov R, Demir N, Kurt M, Tarsuslu T. The Investigation of Relationship between Functional Mobility Levels of Children with Chronic Disability and Caregivers’ Quality of Life. International Journal of Disabilities Sports and Health Sciences. 2023;6(2):218-24.


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