Skip to main content
Iranian Journal of Child Neurology logoLink to Iranian Journal of Child Neurology
. 2017 Autumn;11(4):52–57.

Does Parent Report Gross Motor Function Level of Cerebral Palsy Children Impact on the Quality of Life in these Children?

Marzieh PASHMDARFARD 1, Malek AMINI 2, Reza shervin BADV 3, Narges Ghaffarzade NAMAZI 3, Mehdi RASSAFIANI 4
PMCID: PMC5703629  PMID: 29201124

Abstract

Objective

The aim of this study was to assess the effect of parent report gross motor function level of cerebral palsy (CP) children on the parent report quality of life of CP children.

Materials & Methods

Sampling of this cross-sectional study was done in occupational therapy clinics and CP children’s schools in 2016 in Zanjan, Iran. Samples size was 60 CP children aged 6-12 yr and for sampling method, a non-probability convenience was used. For assessing the quality of life of CP children the cerebral palsy quality of life (CP QOL) questionnaire and for assessing the level of gross motor function of CP children the Gross Motor Function Classification System Family Report Questionnaire (GMFCSFRQ) were used.

Results

The average age of children (22 males and 30 females) was 8.92 yr old (minimum 6 yr and maximum 12 yr). The relationship between the level of gross motor function and participation and physical health was direct and significant (r=0.65). The relationship between functioning, access to services and family health with the level of gross motor function was direct but was not significant (P>0.05) and the relationship between pain and impact of disability and emotional well-being with the level of gross motor function was significant (P<0.05).

Conclusion

There was no strong correlation between the level of gross motor function and quality of life of children with cerebral palsy. It means that the level of gross motor function cannot be used as a predictor of quality of life for children with cerebral palsy alone.

Key Words: Gross motor function, Quality of life, Cerebral palsy

Introduction

Cerebral palsy (CP) is one of the most common childhood disorders that occur in the growing incidence of lesions in the brain (1). The prevalence of CP is approximately 2-2.5 people per 1000 live births (1). It begins early in life, but all affect the scope of one's life (1). Children with CP may experience wide range of disorders such as postural disorders, coordination disorders, sensory and intellectual disorders in their lifetime. Generally, this kind of cognitive and motor impairments which include those factors are most reasons that lead to limiting the children with CP in participating in all life areas (2, 3). Most people with CP are facing with limits on walking and other physical activities. The general idea is that the experience of such restrictions affects people's quality of life (2). Children with CP due to movement restrictions in terms of mobility and self-care are dependent on others and these restrictions affect their participation in activities of daily living (ADL) and consequently affect their quality of life (4-6).

World Health Organization(WHO) defines quality of life as one's perception of his/her own position in relation to the objectives, expectations, values, and concerns, in the cultural and social context in his/her life. Quality of life is a multidimensional structure and is an overall assessment of well-being (2, 7). The United Cerebral Palsy Association (1991) adopted the mission statement: “to affect positively the quality of life of CP children’’ QOL has become the most important outcome of treatments and interventions for children with CP (8).

The main goal of rehabilitation interventions, especially occupational therapy is to improve the quality of life and participation of children with CP in different aspects of life areas (9). Since the main problems of children with CP are disorders such as walking and manipulation, and particularly more focus of rehabilitation interventions and occupational therapy is on motor components such as strength and flexibility of muscles and joints, the question arises that, is focusing on promoting skills and motor components of children with CP ultimately leads to improvement of their quality of life or not? Therefore, this study aimed to determine the relationship between the level of Gross Motor Function of children with CP and their level of quality of life.

Materials & Methods:

The sample size in this study was 60 parents of children with CP. In this cross-sectional study, the sampling was done in occupational therapy clinics and exceptional children’s schools in 2016 in Zanjan, Iran.

The project proposal legislated with the ethics code ‘ZUMS.REC.1395.75’ in Zanjan University of Medical Sciences. Then an introduction letter from Zanjan University of Medical Sciences was taken and referred to occupational therapy clinics and exceptional children’s schools for sampling and getting information of them.

In this study, a non-probability convenience sampling method was used. This means that after attending the clinics and schools, children who had inclusion criteria of this study were enrolled (Table 1).

Table 1.

Inclusion and exclusion criteria

Inclusion criteria Exclusion criteria
Age range of children be 6-12 yr old Not wanting to continue collaborating in the study
Children diagnosed by a neurologist or pediatric neurologist to be a cerebral palsy patient Failure to complete the full questionnaire
Not Having epilepsy or seizure disorder that is resistant to treatment Filling the questionnaire by others instead of the parents or caregivers of CP children
Lack of other disorders such as progressive neuromuscular disorders
Not having Orthopedic surgical pathology and Botox injections in the past 12 months
Lack of blindness and deafness
Having the IQ over than 70%

First of all the consent forms were taken from the parents of children with CP and after those two questionnaires: (Cerebral Palsy Quality of Life (CP QOL) and GMFCS Family Report Questionnaire) were completed by CP children parents’ randomly. The two questionnaires were given to 60 parents of children with CP that had inclusions criteria, but because the 8 of these samples did not complete the questionnaire, were excluded from study and finally, 52 samples remained for final analysis.

Outcome measures

CP QOL: In order to collect information about the quality of life of children with CP, CP QOL questionnaire was used. Validity and reliability of this questionnaire in Iran were assessed, that test-retest reliability for the subscales has been reported 0.74- 0.84(10). CP QOL Questionnaire has 65 items that assesses the CP children’s quality of life in 7 categories: (Social well-being and acceptance (12 items), Functioning (12 items), Participation and physical health (11 items), Emotional well-being (6 items), Access to services (12 items), Pain and impact of disability (8 items), Family health (4 items))(10).

GMFCS Family Report Questionnaire: In order to collect information about the level of gross motor function of children with CP, GMFCS Family Report Questionnaire was used (11). Validity and reliability of this questionnaire in Iran were assessed, and the Intraclass Correlation Coefficient (ICC=0.92) for the total score of the questionnaire was reported (12). GMFCS Family Report Questionnaire is an observational standard classification system that categorizes children with CP in 5 levels based on the current gross motor abilities, limitations in gross motor functions and the need for technology and assistive devices (11).

Data analysis method

For data analysis, the SPSS ver. 21 (Chicago, IL, USA) was used. To determine the normal distribution of data, the Kolmogorov-Smirnov test (K-S) and to measure the relationship between variables, Spearman correlation test was used.

Results

Descriptive Statistics

The mean age of children was 8.92 yr (min: 6 and max: 12 yr), and 22 of the children were male and 30 were female (Table 2).

Table 2.

Democratic characteristic of samples

Frequency Percent (100%)
Age (yr) 6 yr old 5 9.6
7 yr old 9 17.3
8 yr old 9 17.3
9 yr old 9 17.3
10 yr old 8 15.4
11 yr old 6 11.5
12 yr old 6 11.5
Gross Motor Function Levels
(GMFCS levels)
I 12 23.1
II 2 3.8
III 6 11.5
IV 15 28.8
V 17 32.7
Gender Male 22 42.3
Female 30 57.7
Type of Cerebral Palsy Hemiplegia 14 26.9
Diplegia 25 48.1
Quadriplegia 13 25.0

Statistics analysis

The data distribution was not normal (P<0.05). To analyze the relationship between variables the Spearman test was used. The results of analysis of the relationship between the level of gross motor function and quality of life of children with CP are given in Table 3. The relationship between participation and physical health with the level of gross motor function was direct and significant (r=0.65). The relationship between functioning, access to services and family health with the level of gross motor function were direct but were not significant (P>0.05). The relationship between pain and impact of disability and emotional well-being with the level of gross motor function was significant (P<0.05) (Table 3).

Table 3.

Correlation between the Domains of CP- QOL, and GMFCS

Domains of CP QOL-Child P r2 (%) r SD Mean n
Social well-being and acceptance 0.03 7.8 0.28** 21.09 101.57 52
Functioning 0.21 2.5 0.16 8.45 32.94 52
Participation and physical health 0.00 42 0.65** 22.39 91.26 52
Emotional well being 0.002 16 -0.41** 6.18 4.48 52
Pain and impact of disability 0.01 10 -0.33** 14.66 41.55 52
Access to service 0.41 1.4 0.12 15.49 41.90 52
Family health 0.71 0.16 0.04 8.78 28.09 52
**

P<0.05

Discussion

The aim of this study was to examine the relationship between the level of gross motor function and quality of life of children with CP in Zanjan, Iran. The quality of life of children with CP is lower than to healthy peers (12). The best way to assess the quality of life of children with CP is using a questionnaire that is able to measure the quality of life of children with CP in all physical, psychological, social, and other aspects of their life (13). For achieving more accuracy, the parent report version of CP QOL-Child questionnaire was used. The results of this study showed that the relationship between social well-being and acceptance item of quality of life with gross motor function level of CP children was weak; this result is similar to another study (14).

Social well-being and acceptance item of quality of life may be influenced by the factors such as culture, economic level, and social context. In this study, the relationship between the participation and physical health with the level of gross motor function was direct and significant that is consistent with the study in Hamedan, Iran (14). According to the results, in the procedure of rehabilitation, if the therapists pay attention to promoting the gross motor functions and skills of CP children, their participation skills, and their physical well-being will improve, especially the skills that need more mobility. The items of participation and physical health consist the activities that require movement and mobility. The significant correlation of participation and physical health with the level of gross motor function is unexpected. Nevertheless, the relationship between functioning, access to services and family health with the level of gross motor function were direct but were not significant and the relationship between them is so weak.

The CP children’s quality of life is a multidimensional concept influenced by many factors such as physical status, environmental issues and context and factors such as the level of gross motor function and the level of spasticity have much less impact on quality of life (15). Therefore, occupational therapists should not pay attention only to the Gross motor function of children with CP, and they have to pay attention to other concepts of their quality of life by environmental adaptations, educating the parents and caregivers etc. therapists by conducting a comprehensive and multidimensional intervention can promote the CP children’s quality of life. However, the improvement in gross motor skills of children with CP affects improving the quality of life in all aspects of the physical and psychological life (5). The quality of life of children with CP and their parents are lower than their healthy peers are, but the factors that affect the CP children’s quality of life and the factors that affect their parent’s quality of life are different.

The main factors that affect the children with CP quality of life are as follows: Low levels of health and socioeconomic levels compared to healthy peers. In addition, the main factors that affect their parents quality of life are difficulty in accessing to rehabilitation services, low level of socio economic status, and their children’s disability, but there is not any relationship between the severity of disability and their parent’s quality of life (16). The quality of life of children with CP in all aspect of life areas (physical and psychosocial) are similar to their healthy peers but the level of their parent’s quality of life is lower than other parents, and the probable reason was because of the low level of gross motor function of children with CP and their disability compared with healthy children (17). Different results may be because of cultural and attitudinal factors that govern the society. The relationship between pain and impact of disability with the level of gross motor function was significant but diverse; likely whatever the level of gross motor function of children with CP is high the level of pain and the impact of pain on disability are low. The result of this study is aligned with other that indicated the main reason for the low quality of life of children with CP is pain (18). The significant relationship between pain and gross motor function of children with CP may be because, when the level of gross motor function is low and the severity of spasticity is high then the mobility of the body will decrease and the probability of deformity and contracture rises out and these factors can increase the feeling of pain. Using GMFCS and the level of gross motor function in children with CP were good predictor of quality of life of the CP children's parents, not the children with CP (19).

In Conclusion, there is not a strong correlation between level of gross motor function and quality of life of children with CP (20). It should be considered on the treatment of these children that the level of gross motor function could not be alone a predictor of quality of life of children with CP. In the rehabilitation interventions of children with CP, occupational therapists should not focus only on gross motor function of children with CP but also for promoting the quality of life of these children, they have to pay attention to the cultural, environmental, economic, social and physical condition of children with CP and their parents and caregivers.

Conflict of Interest

The authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Acknowledgment

This study was funded by a grant from Deputy of Research and Technology Zanjan University of Medical Sciences (ZUMS), (Grant No: A-11-1097-1), Iran. Thereby authors thank and appreciate the cerebral palsy children and families who participated in this study.

Authors’ contribution

Marzieh Pashmdarfard and Malek Amini, project design and supervise, final approval of the version to be published and interpreting and discussing results.

Reza shervin Badv and Narges Ghaffarzade Namazi, data collection.

Mehdi Rassafiani, providing the assessment tools of study.

All authors agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

References

  • 1.Lim Y, Seer M, Wong C. Impact of cerebral palsy on the quality of life in patients and their families. Neurol Asia. 2009;14:27–33. [Google Scholar]
  • 2.Bjornson K, Belza B, Kartin D, Logsdon R, McLaughlin J. Self-reported health status and quality of life in youth with cerebral palsy and typically developing youth. Arch Phys Med Rehab. 2008;89:121–7. doi: 10.1016/j.apmr.2007.09.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.White‐Koning M, Grandjean H, Colver A, Arnaud C. Parent and professional reports of the quality of life of children with cerebral palsy and associated intellectual impairment. Dev Med Child Neurol. 2008;50:618–24. doi: 10.1111/j.1469-8749.2008.03026.x. [DOI] [PubMed] [Google Scholar]
  • 4.Kennes J, Rosenbaum P, Hanna S, Walter S, Russell D, Raina P. Health status of school aged children with cerebral palsy: information from a populationbased sample. Dev Med Child Neurol. 2002;44(4):240–7. doi: 10.1017/s0012162201002018. [DOI] [PubMed] [Google Scholar]
  • 5.Kerr C, McDowell B, McDonough S. The relationship between gross motor function and participation restriction in children with cerebral palsy: an exploratory analysis. Child Care Hlth Dev. 2007;33(1):22–7. doi: 10.1111/j.1365-2214.2006.00634.x. [DOI] [PubMed] [Google Scholar]
  • 6.Mehraban AH, Hassani M, Amini M. The Comparison of Participation in School-Aged Cerebral Palsy Children and normal Peers: A Preliminary Study. Iran J Pediatr. 2016;26(3):e5303. doi: 10.5812/ijp.5303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Bonomi A, Patrick D, Bushnell D, Martin M. Validation of the United States' version of the World Health Organization Quality of Life (WHOQOL) instrument. J Clin Epidemiol. 2000;53(1):1–12. doi: 10.1016/s0895-4356(99)00123-7. [DOI] [PubMed] [Google Scholar]
  • 8.Bjornson K, McLaughlin J. The measurement of healthrelated quality of life (HRQL) in children with cerebral palsy. Eur J Neurol. 2001;8(5):183–93. doi: 10.1046/j.1468-1331.2001.00051.x. [DOI] [PubMed] [Google Scholar]
  • 9.Pashmdarfard M, Amini M, Hassani Mehraban A. Participation of Iranian Cerebral Palsy Children in Life Areas: A Systematic Review. Iran J Child Neurol. 2017;11(1):1–12. [PMC free article] [PubMed] [Google Scholar]
  • 10.Soleimani F, Vameghi R, Kazemnejad A, Fahimi NA, Nobakht Z, Rassafiani M. Psychometric Properties of the Persian Version of Cerebral Palsy Quality of Life Questionnaire for Children. Iran J Child Neurol. 2015;9(1):76–86. [PMC free article] [PubMed] [Google Scholar]
  • 11.Riahi A, Rassafiani M, Binesh M. the cross- cultural validation and Test-retest and Inter Rater reliability of parent version of the Gross Motor Function Classification System for children with cerebral palsy. J Rehab. 2013;13(5):25–30. [Google Scholar]
  • 12.Tuzun E, Eker L, Daskapan A. An assessment of the impact of cerebral palsy on childrens quality of life. Fizyoterapi Rehabilitasyon. 2004;15(1):3–8. [Google Scholar]
  • 13.Livingston M, Rosenbaum P, Russell D, Palisano R. Quality of life among adolescents with cerebral palsy: what does the literature tell us? Dev Med Child Neurol. 2007;49(3):225–31. doi: 10.1111/j.1469-8749.2007.00225.x. [DOI] [PubMed] [Google Scholar]
  • 14.NuraniGharaborghe S, Sarhady M, Hosseini S, Mortazavi SS. Relationship between Quality of Life and Gross Motor Function in Children with Cerebral Palsy age 4-12. Medical Journal of Tabriz University of Medical Sciences and Health Services. 2015;37(2):48–5. [Google Scholar]
  • 15.Dehno N, Dehkordi S, Dadgoo M, Salehi M. Association between spasticity and the level of motor function with quality of life in community dwelling Iranian young adults with spastic cerebral palsy. Med J Islam Repub Iran. 2012;26(4):150–6. [PMC free article] [PubMed] [Google Scholar]
  • 16.Mohammed F, Ali S, Mustafa M. 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):355–61. doi: 10.4103/0976-3147.182778. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Böling S, Varho T, Kiviranta T, Haataja L. Quality of life of Finnish children with cerebral palsy. Disabil Rehabil. 2016;38(7):683–8. doi: 10.3109/09638288.2015.1061607. [DOI] [PubMed] [Google Scholar]
  • 18.Nilsson S, Johnson E, Adolfsson M. Professionals' Perceptions about the Need for Pain Management Interventions for Children with Cerebral Palsyin South African School Settings. Pain Manag Nurs. 2016;17(4):249–61. doi: 10.1016/j.pmn.2016.03.002. [DOI] [PubMed] [Google Scholar]
  • 19.Surender S, Gowda V, Sanjay K, Basavaraja G, Benakappa N, Benakappa A. Caregiver-reported health-related quality of life of children with cerebral palsy and their families and its association with gross motor function: A South Indian study. J Neurosci Rural Pract. 2016;7(22):23–7. doi: 10.4103/0976-3147.178657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Naghdi S, Ansari NN, Raji P, Shamili A, Amini M, Hasson S. Cross-cultural validation of the Persian version of the Functional Independence Measure for patients with stroke. Disability and Rehabilitation. 2016;38(3):289–298. doi: 10.3109/09638288.2015.1036173. [DOI] [PubMed] [Google Scholar]

Articles from Iranian Journal of Child Neurology are provided here courtesy of Shahid Beheshti University of Medical Sciences

RESOURCES