Klinik Araştırma
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Relationship Between Child, Caregiver Characteristics and Caregiver Fatigue and Quality of Life Parameters in Children with Cerebral Palsy

Yıl 2025, Cilt: 15 Sayı: 3, 401 - 408, 24.09.2025
https://doi.org/10.33631/sabd.1529710

Öz

Aim: The aim of the study is to examine caregiver fatigue and quality of life in children with cerebral palsy (CP) with and without ambulation according to the sociodemographic characteristics of the child and caregiver.
Material and Methods: 60 children with CP and their caregivers included in the study. After sociodemographic information of children with CP and caregivers were recorded, gross motor function levels of individuals were classified according to Gross Motor Classification System (GMFCS). GMFCS levels I and II were grouped as ambulatory, and levels III, IV and V as non-ambulatory. Functional independence levels of children were assessed with Functional Independence Measure for Children (weeFIM), fatigue level of caregivers was assessed with Fatigue Severity Scale (FSS), and quality of life parameters including pain, physical activity, energy level, sleep, social isolation, and emotional reactions were assessed with Nottingham Health Profile (NHP).
Results: In the ambulatory group, there was a statistically significant positive correlation between the fatigue level of the caregiver and the duration of the child's participation in the physiotherapy (r=0.333, p=0.038,) and age (r=0.406, p=0.010). In the non-ambulatory group, there was a statistically significant positive correlation between the caregiver's age (r=0.500, p=0.021), body mass index (r=0.748, p<0.001), child’s age (r=0.500, p=0.021), duration of the child's participation in the physiotherapy (r=0.459, p=0.036) and fatigue level of the caregiver. In the non-ambulatory group, there was a statistically significant positive correlation between the duration of the child's participation in physiotherapy and the caregiver's NHP scores (r=0.437, p=0.047).
Conclusion: In caregivers of ambulatory and non-ambulatory children with CP, duration of the child's participation in physiotherapy is associated with the caregiver's fatigue level. In non-ambulant children, it was concluded that the child's age, body mass index, and duration of the child's participation in the physiotherapy were associated with the caregiver's pain, social isolation and quality of life.

Kaynakça

  • McIntyre S, Goldsmith S, Webb A, Ehlinger V, Hollung SJ, McConnell K, et al. Global prevalence of cerebral palsy: a systematic analysis. Dev Med Child Neurol. 2022;64(12):1494-506.
  • Rosenbaum P, Paneth N, Leviton A, Goldstein M, Bax M. A report: the definition and classification of cerebral palsy April 2006. Dev Med Child Neurol Suppl. 2007;49(109):8-14.
  • Pruitt DW, Tsai T. Common medical comorbidities associated with cerebral palsy. Phys Med Rehabil Clin N Am. 2009;20(3):453-67.
  • Malik BA, Zafar S, Razzaq A, Butt MA, Khan MS, Mughal S. Frequently associated problems of cerebral palsy. Ann Punjab Med Coll. 2007;1(2):14-8.
  • Ones K, Yilmaz E, Cetinkaya B, Caglar N. Assessment of the quality of life of mothers of children with cerebral palsy (primary caregivers). Neurorehabil Neural Repair. 2005;19(3):232-7.
  • Liu F, Shen Q, Huang M, Zhou H. Factors associated with caregiver burden among family caregivers of children with cerebral palsy: a systematic review. BMJ Open. 2023;13(4):e065215.
  • Albayrak I, Biber A, Çalışkan A, Levendoglu F. Assessment of pain, care burden, depression level, sleep quality, fatigue and quality of life in the mothers of children with cerebral palsy. J Child Health Care. 2019;23(3):483-94.
  • Garip Y, Ozel S, Tuncer OB, Kilinc G, Seckin F, Arasil T. Fatigue in the mothers of children with cerebral palsy. Disabil Rehabil. 2017;39(8):757-62.
  • Mohammed SS, Abdelwahab MS, Zaky NA, Abdelazeim FH. Impact of mother’s care burden, fatigue and Child’s functional level on quality of life in spastic cerebral palsy. Physiother Res Int. 2024;29(1):e2067.
  • Khayatzadeh MM, Rostami HR, Amirsalari S, Karimloo M. Investigation of quality of life in mothers of children with cerebral palsy in Iran: association with socio-economic status, marital satisfaction and fatigue. Disabil Rehabil. 2013;35(10):803-8.
  • Agiati E, Huripah E. Burnout of parent who have children with cerebral palsy disability in bandung city. Asian Soc Work J. 2019;4(2):35-43.
  • Yun C-K. Relationship between the quality of life of the caregiver and motor function of children with cerebral palsy. Phys Ther Rehabil Sci. 2017;6(1):26-32.
  • Tseng M-H, Chen K-L, Shieh J-Y, Lu L, Huang C-Y, Simeonsson RJ. Child characteristics, caregiver characteristics, and environmental factors affecting the quality of life of caregivers of children with cerebral palsy. Disabil Rehabil. 2016;38(24):2374-82.
  • Mohammed FMS, Ali SM, Mustafa MAA. Quality of life of cerebral palsy patients and their caregivers: a cross sectional study in a rehabilitation center Khartoum-Sudan (2014–2015). J Neurosci Rural Pract. 2016;7(3):355.
  • Palisano R, Rosenbaum P, Barlett D, Livingston M. Kaba motor fonksiyon sınıflandırma sistemi (genişletilmiş ve yeniden düzenlenmiş şekli). Kerem Günel M, Mutlu A, Livanelioğlu A, El Ö, Baydar M, Peker Ö, et al. translators. CanChild Centre for Childhood Disability Research, McMaster University; 2007 [cited 2025 Sep 21]. Available from: https://www.bobathterapistleri.org/resimekleme/Belge/2152020223841911.pdf
  • Palisano R, Rosenbaum P, Walter S, Russell D, Wood E, Galuppi B. Gross motor function classification system for cerebral palsy. Dev Med Child Neurol. 1997;39(4):214-23.
  • Ottenbacher KJ, Msall ME, Lyon NR, Duffy LC, Granger C V, Braun S. Interrater agreement and stability of the functional independence measure for children (weefimTM): use in children with developmental disabilities. Arch Phys Med Rehabil. 1997;78(12):1309-15.
  • Aybay C, Erkin G, Elhan AH, Sirzai H, Ozel S. ADL assessment of nondisabled Turkish children with the WeeFIM instrument. Am J Phys Med Rehabil. 2007;86(3):176-82.
  • Tur BS, Küçükdeveci AA, Kutlay Ş, Yavuzer G, Elhan AH, Tennant A. Psychometric properties of the WeeFIM in children with cerebral palsy in Turkey. Dev Med Child Neurol. 2009;51(9):732-8.
  • Krupp LB, Larocca NG, Muir Nash J, Steinberg AD. The fatigue severity scale: application to patients with multiple sclerosis and systemic lupus erythematosus. Arch Neurol. 1989;46(10):1121-3.
  • Armutlu K, Korkmaz NC, Keser I, Sumbuloglu V, Akbiyik DI, Guney Z, et al. The validity and reliability of the Fatigue Severity Scale in Turkish multiple sclerosis patients. Int J Rehabil Res. 2007;30(1):81-5.
  • Gencay-Can A, Can SS. Validation of the Turkish version of the fatigue severity scale in patients with fibromyalgia. Rheumatol Int. 2012;32(1):27-31.
  • Hunt S, McKenna SP, McEwen J. The Nottingham Health Profile user’s manual. revised ed. Manchester University Press; 1989.
  • Kücükdeveci AA, McKenna SP, Kutlay S, Gürsel Y, Whalley D, Arasil T. The development and psychometric assessment of the Turkish version of the Nottingham Health Profile. Int J Rehabil Res. 2000;23(1):31-8.
  • Schober P, Boer C, Schwarte LA. Correlation coefficients: appropriate use and interpretation. Anesth Analg. 2018;126(5):1763-8.
  • Ahmadizadeh Z, Rassafiani M, Khalili MA, Mirmohammadkhani M. Factors associated with quality of life in mothers of children with cerebral palsy in Iran. Hong Kong J Occup Ther. 2015;25:15-22.
  • Aaronson LS, Teel CS, Cassmeyer V, Neuberger GB, Pallikkathayil L, Pierce J, et al. Defining and measuring fatigue. Image J Nurs Scholarsh. 1999;31(1):45-50.
  • Ersin I, Yumin ET, Turkoglu SA. An investigation of factors affecting quality of life in parents of chronically disabled children. Ann Med Res. 2022;29(6):574-9.
  • Pasin T, Dogruoz Karatekin B, Pasin O. Chronic fatigue syndrome in caregivers of children with cerebral palsy and affecting factors. North Clin Istanbul. 2023;10(5): 642-650.
  • Marrón EM, Redolar-Ripol D, Boixadós M, Nieto R, Guillamón N, Hernández E, et al. Burden on caregivers of children with cerebral palsy: predictors and related factors. Univ Psychol. 2013;12(3):767-77.
  • Singogo C, Mweshi M, Rhoda A. Challenges experienced by mothers caring for children with cerebral palsy in Zambia. S Afr J Physiother. 2015;71(1):274.
  • Davis E, Shelly A, Waters E, Boyd R, Cook K, Davern M. The impact of caring for a child with cerebral palsy: quality of life for mothers and fathers. Child Care Health Dev. 2010;36(1):63-73.
  • Mwinbam MM, Suglo JN, Agyeman YN, Kukeba MW. Family caregivers’ experience of care with a child with cerebral palsy: the lived experiences and challenges of caregivers in a resource-limited setting in northern Ghana. BMJ Paediatr Open. 2023;7(1):e001807.
  • Dlamini MD, Chang Y-J, Nguyen TTB. Caregivers’ experiences of having a child with cerebral palsy. A meta-synthesis. J Pediatr Nurs. 2023;73:157-68.
  • Bursalı A, Güngör S. Serebral palsi ve aile (anne, kıdemli ortopedi ve travmatoloji uzmanı ile psikolog gözüyle serebral palsi). TOTBID Derg. 2021;20(3): 362-365.
  • Demircioğlu G, Atılgan E, Tarakcı D. Hastane ve özel eğitim ortamında fizyoterapi hizmeti alan Serebral palsi’li çocukların ailelerinin beklentileri, stres ve memnuniyet düzeylerinin araştırılması. Sağlık Bilim Meslek Derg. 2018;5(19):288-94.
  • Hurvitz EA, Green LB, Hornyak JE, Khurana SR, Koch LG. Body mass index measures in children with cerebral palsy related to gross motor function classification: a clinic-based study. Am J Phys Med Rehabil. 2008;87(5):395-403.
  • Gugała B. Caregiver burden versus intensity of anxiety and depression symptoms in parents of children with cerebral palsy as well as factors potentially differentiating the level of burden: a cross-sectional study (Poland). BMJ Open. 2021;11(6): e036494.
  • Gokcin Eminel A, Kahraman T, Genc A. Physical workload during caregiving activities and related factors among the caregivers of children with cerebral palsy. Ir J Med Sci. 2021;190(2):701-9.
  • Terzi R, Tan G. Musculoskeletal system pain and related factors in mothers of children with cerebral palsy. Agri. 2016;28(1):18-24.
  • Farajzadeh A, Maroufizadeh S, Amini M. Factors associated with quality of life among mothers of children with cerebral palsy. Int J Nurs Pract. 2020;26(3):1-9.
  • Glinac A, Matović L, Delalić A, Mešalić L. Quality of life in mothers of children with cerebral palsy. Acta Clin Croat. 2017;56(2):299-307.
  • Eker L, Tüzün EH. An evaluation of quality of life of mothers of children with cerebral palsy. Disabil Rehabil. 2004;26(23):1354-9.
  • Terra VC, Cysneiros RM, Schwartzman JS, Teixeira MCTV, Arida RM, Cavalheiro EA, et al. Mothers of children with cerebral palsy with or without epilepsy: a quality of life perspective. Disabil Rehabil. 2011;33(5):384-8.

Serebral Palsili Çocuklarda Çocuk ve Bakım Veren Özellikleri ile Bakım Verenin Yorgunluk ve Yaşam Kalitesi Parametreleri Arasındaki İlişki

Yıl 2025, Cilt: 15 Sayı: 3, 401 - 408, 24.09.2025
https://doi.org/10.33631/sabd.1529710

Öz

Amaç: Çalışmanın amacı ambule olan ve olmayan Serebral Palsili (SP) çocuklarda, çocuk ve bakım verenin sosyodemografik özelliklerine göre bakım verenin yorgunluk ve yaşam kalitesini incelemektir.
Gereç ve Yöntemler: Çalışmaya SP tanısı almış 60 çocuk ve bakım veren dahil edildi. SP’li çocukların ve bakım verenlerin sosyodemografik bilgileri kaydedildikten sonra çocukların kaba motor fonksiyon düzeyleri Kaba Motor Fonksiyon Sınıflama Sistemi’ne (KMFSS) göre sınıflandırıldı. KMFSS seviye 1, 2 ve 3 olanlar ambule, seviye 4 ve 5 olanlar ambule olmayan olarak gruplandırıldı. Çocukların fonksiyonel bağımsızlık düzeyleri Çocuklar için Fonksiyonel Bağımsızlık Ölçütü (ÇİFBÖ) ile, bakım verenin yorgunluk düzeyi, Yorgunluk Şiddeti Ölçeği (YŞÖ) ile; ağrı, fiziksel aktivite, enerji düzeyi, uyku, sosyal izolasyon, emosyonel reaksiyonlar gibi yaşam kalitesi parametreleri Nottingham Sağlık Profili (NSP) ile değerlendirildi.
Bulgular: Ambule grupta bakım verenin yorgunluk düzeyi ile çocuğun fizyoterapi alma yılı (r=0,333, p=0,038,) ve yaşı (r=0,406, p= 0,010) arasında pozitif yönde istatistiksel olarak anlamlı korelasyon vardı. Ambule olmayan grupta bakım verenin yaşı (r=0,500, p=0,021), vücut kitle indeksi (r=0,748, p<0,001), çocuğun yaşı (r=0,500, p=0,021), çocuğun fizyoterapi alma yılı (r=0,459, p=0,036) ile bakım verenin yorgunluk düzeyi arasında pozitif yönde istatistiksel olarak anlamlı korelasyon vardı. Ambule olmayan grupta çocuğun fizyoterapi alma yılı ile bakım verenin NSP puanları arasında pozitif yönde istatistiksel olarak anlamlı korelasyon vardı (r=0,437, p=0,047).
Sonuç: Ambule olan ve olmayan SP’li çocuğa bakım verenlerde, çocuğun fizyoterapi alma yılı ile bakım verenin yorgunluk düzeyi ilişkilidir. Ambule olmayan çocuklarda çocuğun yaşının, vücut kitle indeksinin, fizyoterapi alma yılının bakım verenin ağrısı, sosyal izolasyonu ve yaşam kalitesi ile ilişkili olduğu sonucuna ulaşıldı.

Kaynakça

  • McIntyre S, Goldsmith S, Webb A, Ehlinger V, Hollung SJ, McConnell K, et al. Global prevalence of cerebral palsy: a systematic analysis. Dev Med Child Neurol. 2022;64(12):1494-506.
  • Rosenbaum P, Paneth N, Leviton A, Goldstein M, Bax M. A report: the definition and classification of cerebral palsy April 2006. Dev Med Child Neurol Suppl. 2007;49(109):8-14.
  • Pruitt DW, Tsai T. Common medical comorbidities associated with cerebral palsy. Phys Med Rehabil Clin N Am. 2009;20(3):453-67.
  • Malik BA, Zafar S, Razzaq A, Butt MA, Khan MS, Mughal S. Frequently associated problems of cerebral palsy. Ann Punjab Med Coll. 2007;1(2):14-8.
  • Ones K, Yilmaz E, Cetinkaya B, Caglar N. Assessment of the quality of life of mothers of children with cerebral palsy (primary caregivers). Neurorehabil Neural Repair. 2005;19(3):232-7.
  • Liu F, Shen Q, Huang M, Zhou H. Factors associated with caregiver burden among family caregivers of children with cerebral palsy: a systematic review. BMJ Open. 2023;13(4):e065215.
  • Albayrak I, Biber A, Çalışkan A, Levendoglu F. Assessment of pain, care burden, depression level, sleep quality, fatigue and quality of life in the mothers of children with cerebral palsy. J Child Health Care. 2019;23(3):483-94.
  • Garip Y, Ozel S, Tuncer OB, Kilinc G, Seckin F, Arasil T. Fatigue in the mothers of children with cerebral palsy. Disabil Rehabil. 2017;39(8):757-62.
  • Mohammed SS, Abdelwahab MS, Zaky NA, Abdelazeim FH. Impact of mother’s care burden, fatigue and Child’s functional level on quality of life in spastic cerebral palsy. Physiother Res Int. 2024;29(1):e2067.
  • Khayatzadeh MM, Rostami HR, Amirsalari S, Karimloo M. Investigation of quality of life in mothers of children with cerebral palsy in Iran: association with socio-economic status, marital satisfaction and fatigue. Disabil Rehabil. 2013;35(10):803-8.
  • Agiati E, Huripah E. Burnout of parent who have children with cerebral palsy disability in bandung city. Asian Soc Work J. 2019;4(2):35-43.
  • Yun C-K. Relationship between the quality of life of the caregiver and motor function of children with cerebral palsy. Phys Ther Rehabil Sci. 2017;6(1):26-32.
  • Tseng M-H, Chen K-L, Shieh J-Y, Lu L, Huang C-Y, Simeonsson RJ. Child characteristics, caregiver characteristics, and environmental factors affecting the quality of life of caregivers of children with cerebral palsy. Disabil Rehabil. 2016;38(24):2374-82.
  • Mohammed FMS, Ali SM, Mustafa MAA. Quality of life of cerebral palsy patients and their caregivers: a cross sectional study in a rehabilitation center Khartoum-Sudan (2014–2015). J Neurosci Rural Pract. 2016;7(3):355.
  • Palisano R, Rosenbaum P, Barlett D, Livingston M. Kaba motor fonksiyon sınıflandırma sistemi (genişletilmiş ve yeniden düzenlenmiş şekli). Kerem Günel M, Mutlu A, Livanelioğlu A, El Ö, Baydar M, Peker Ö, et al. translators. CanChild Centre for Childhood Disability Research, McMaster University; 2007 [cited 2025 Sep 21]. Available from: https://www.bobathterapistleri.org/resimekleme/Belge/2152020223841911.pdf
  • Palisano R, Rosenbaum P, Walter S, Russell D, Wood E, Galuppi B. Gross motor function classification system for cerebral palsy. Dev Med Child Neurol. 1997;39(4):214-23.
  • Ottenbacher KJ, Msall ME, Lyon NR, Duffy LC, Granger C V, Braun S. Interrater agreement and stability of the functional independence measure for children (weefimTM): use in children with developmental disabilities. Arch Phys Med Rehabil. 1997;78(12):1309-15.
  • Aybay C, Erkin G, Elhan AH, Sirzai H, Ozel S. ADL assessment of nondisabled Turkish children with the WeeFIM instrument. Am J Phys Med Rehabil. 2007;86(3):176-82.
  • Tur BS, Küçükdeveci AA, Kutlay Ş, Yavuzer G, Elhan AH, Tennant A. Psychometric properties of the WeeFIM in children with cerebral palsy in Turkey. Dev Med Child Neurol. 2009;51(9):732-8.
  • Krupp LB, Larocca NG, Muir Nash J, Steinberg AD. The fatigue severity scale: application to patients with multiple sclerosis and systemic lupus erythematosus. Arch Neurol. 1989;46(10):1121-3.
  • Armutlu K, Korkmaz NC, Keser I, Sumbuloglu V, Akbiyik DI, Guney Z, et al. The validity and reliability of the Fatigue Severity Scale in Turkish multiple sclerosis patients. Int J Rehabil Res. 2007;30(1):81-5.
  • Gencay-Can A, Can SS. Validation of the Turkish version of the fatigue severity scale in patients with fibromyalgia. Rheumatol Int. 2012;32(1):27-31.
  • Hunt S, McKenna SP, McEwen J. The Nottingham Health Profile user’s manual. revised ed. Manchester University Press; 1989.
  • Kücükdeveci AA, McKenna SP, Kutlay S, Gürsel Y, Whalley D, Arasil T. The development and psychometric assessment of the Turkish version of the Nottingham Health Profile. Int J Rehabil Res. 2000;23(1):31-8.
  • Schober P, Boer C, Schwarte LA. Correlation coefficients: appropriate use and interpretation. Anesth Analg. 2018;126(5):1763-8.
  • Ahmadizadeh Z, Rassafiani M, Khalili MA, Mirmohammadkhani M. Factors associated with quality of life in mothers of children with cerebral palsy in Iran. Hong Kong J Occup Ther. 2015;25:15-22.
  • Aaronson LS, Teel CS, Cassmeyer V, Neuberger GB, Pallikkathayil L, Pierce J, et al. Defining and measuring fatigue. Image J Nurs Scholarsh. 1999;31(1):45-50.
  • Ersin I, Yumin ET, Turkoglu SA. An investigation of factors affecting quality of life in parents of chronically disabled children. Ann Med Res. 2022;29(6):574-9.
  • Pasin T, Dogruoz Karatekin B, Pasin O. Chronic fatigue syndrome in caregivers of children with cerebral palsy and affecting factors. North Clin Istanbul. 2023;10(5): 642-650.
  • Marrón EM, Redolar-Ripol D, Boixadós M, Nieto R, Guillamón N, Hernández E, et al. Burden on caregivers of children with cerebral palsy: predictors and related factors. Univ Psychol. 2013;12(3):767-77.
  • Singogo C, Mweshi M, Rhoda A. Challenges experienced by mothers caring for children with cerebral palsy in Zambia. S Afr J Physiother. 2015;71(1):274.
  • Davis E, Shelly A, Waters E, Boyd R, Cook K, Davern M. The impact of caring for a child with cerebral palsy: quality of life for mothers and fathers. Child Care Health Dev. 2010;36(1):63-73.
  • Mwinbam MM, Suglo JN, Agyeman YN, Kukeba MW. Family caregivers’ experience of care with a child with cerebral palsy: the lived experiences and challenges of caregivers in a resource-limited setting in northern Ghana. BMJ Paediatr Open. 2023;7(1):e001807.
  • Dlamini MD, Chang Y-J, Nguyen TTB. Caregivers’ experiences of having a child with cerebral palsy. A meta-synthesis. J Pediatr Nurs. 2023;73:157-68.
  • Bursalı A, Güngör S. Serebral palsi ve aile (anne, kıdemli ortopedi ve travmatoloji uzmanı ile psikolog gözüyle serebral palsi). TOTBID Derg. 2021;20(3): 362-365.
  • Demircioğlu G, Atılgan E, Tarakcı D. Hastane ve özel eğitim ortamında fizyoterapi hizmeti alan Serebral palsi’li çocukların ailelerinin beklentileri, stres ve memnuniyet düzeylerinin araştırılması. Sağlık Bilim Meslek Derg. 2018;5(19):288-94.
  • Hurvitz EA, Green LB, Hornyak JE, Khurana SR, Koch LG. Body mass index measures in children with cerebral palsy related to gross motor function classification: a clinic-based study. Am J Phys Med Rehabil. 2008;87(5):395-403.
  • Gugała B. Caregiver burden versus intensity of anxiety and depression symptoms in parents of children with cerebral palsy as well as factors potentially differentiating the level of burden: a cross-sectional study (Poland). BMJ Open. 2021;11(6): e036494.
  • Gokcin Eminel A, Kahraman T, Genc A. Physical workload during caregiving activities and related factors among the caregivers of children with cerebral palsy. Ir J Med Sci. 2021;190(2):701-9.
  • Terzi R, Tan G. Musculoskeletal system pain and related factors in mothers of children with cerebral palsy. Agri. 2016;28(1):18-24.
  • Farajzadeh A, Maroufizadeh S, Amini M. Factors associated with quality of life among mothers of children with cerebral palsy. Int J Nurs Pract. 2020;26(3):1-9.
  • Glinac A, Matović L, Delalić A, Mešalić L. Quality of life in mothers of children with cerebral palsy. Acta Clin Croat. 2017;56(2):299-307.
  • Eker L, Tüzün EH. An evaluation of quality of life of mothers of children with cerebral palsy. Disabil Rehabil. 2004;26(23):1354-9.
  • Terra VC, Cysneiros RM, Schwartzman JS, Teixeira MCTV, Arida RM, Cavalheiro EA, et al. Mothers of children with cerebral palsy with or without epilepsy: a quality of life perspective. Disabil Rehabil. 2011;33(5):384-8.
Toplam 44 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Hemşirelik (Diğer)
Bölüm Araştırma Makaleleri
Yazarlar

Sezen Tezcan 0000-0003-4046-9201

Eylem Tütün Yümin 0000-0002-6994-9391

Seda Ayaz Taş 0000-0002-2778-0065

Yayımlanma Tarihi 24 Eylül 2025
Gönderilme Tarihi 7 Ağustos 2024
Kabul Tarihi 19 Ağustos 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 15 Sayı: 3

Kaynak Göster

Vancouver Tezcan S, Tütün Yümin E, Ayaz Taş S. Serebral Palsili Çocuklarda Çocuk ve Bakım Veren Özellikleri ile Bakım Verenin Yorgunluk ve Yaşam Kalitesi Parametreleri Arasındaki İlişki. SABD. 2025;15(3):401-8.