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Quality of Life and Functional Performance in Children With Spastic Cerebral Palsy

Quality of Life and Functional Performance in Children With Spastic Cerebral Palsy in Relation to Care Burden and Fatigue of Their Mothers

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05381233
Enrollment
200
Registered
2022-05-19
Start date
2022-01-01
Completion date
2024-07-15
Last updated
2022-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Evaluations

Brief summary

Caregiver Burden (CB) is expressed as a multidimensional response related to caregiving, including physical, psychological, emotional, social, and economic problems and has been identified as a public health concern. All these factors negatively affect caregiver health and indirectly affect the care of the disabled child .To provide better support for parents of children with CP, we must understand the difficulties faced those parents and identify the key and common areas where assistance can be rendered.

Detailed description

The symptoms of CP vary from person to person. A person with severe CP might need to use special equipment to be able to walk, or might not be able to walk at all and might need lifelong care. A person with mild CP, on the other hand, might walk a little awkwardly, but might not need any special help. CP does not get worse over time, though the exact symptoms can change over a person's lifetime.

Interventions

OTHERArabic Version of Zarit burden Inventory measure

assessment

OTHERArabic Version of Chalder Fatigue Scale (CFQ version 11)

assessment

Sponsors

Sara Shawki Mohamed
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
2 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Age older then 18 years. * there BMI will be ranged from 18.5 too 24.9 kg/m2 (Misra et al., 2009) . * They are the main caregiver for there children. * They are of low or middle socioeconomic status according too socioeconomic status scale (El-Gilany et al., 2012). * Having at least 7months of experience in taking care of the child. * They have no congenital spinal anomalies or lower limb deformities.

Exclusion criteria

* Children wif congenital anomalies and chromosomal disease. * Children wif recent musculoskeletal surgery. * Any associated problems.

Design outcomes

Primary

MeasureTime frameDescription
Gross motor function classification System (GMFCS)3 monthsWhich are a Standardized method too, classify gross motor function in children with (CP) aged from 2 too, 18years. Teh GMFCS are a 5-level system designed too, reflect differences in gross motor function that are meaningful in teh daily lives of children with CP and there families, with an emphasis on sitting and walking. A classification are made by determining which level best corresponds too, a childs present gross motor function (Palisano et al., 1997). dis scale will be used for detecting teh CP child functional performance level
Arabic Version of Zarit burden Inventory measure3 monthsIt are one of the most commonly used measures of caregiver burden (Knight et al., 2000). The care burden of all the participants will be evaluated by the Zarit burden Inventory measures (ZBI). The ZBI assesses the stress suffered by those whom give care too the persons in need. Initially developed and validated more TEMPthan 25 years ago (Zarit et al., 1980)

Countries

Egypt

Contacts

Primary Contactemad ismail, doctoral
emad9111@live.com01146808839

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026