Skip to main content
OpenTrials
Completed

NCT Number: NCT06443398

Spine of Caregivers of Children with Cerebral Palsy

The purpose of this study was to assess pain (rest, activity, and night pain using the Visual Analog Scale), disability (neck using the Neck Disability Index; lumbar using the Oswestry Disability Index), and curvature (cervical, thoracic, and lumbar using the Spinal Mouse) in primary caregivers of children with cerebral palsy.

Completed

Looking for future studies?

Notify Me

Key information

Age range

25 year–54 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Kırşehir Ahi Evran University Physical Therapy and Rehabilitation Center

Kırşehir, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Primary caregiver between the ages of 25-54
  • Has a child diagnosed with Cerebral Palsy between the ages of 0-18
  • Does not have inflammatory pain
  • Without pain originating from abdominal-pelvic organs
  • Volunteer caregivers were included

Exclusion criteria

  • Having acute fracture and malignancy
  • Had a surgical operation (related to spine disorders)
  • Having a care burden for more than one disabled individual
  • Caregivers with chronic illnesses (such as neurological, psychological disorders) were excluded

Treatment and study plan

There is no intervention in the study

Other

There is no intervention in the study

Primary outcomes

  1. Life Quality

    Time frame: 16 week

    Parents' quality of life was measured using the Nottingham Health Profile. The scale has two parts. 0 represents the best health status, 100 the worst. Score on the scale and health status have an inverse relationship. As the score increases, the health status deteriorates.

  2. Disability

    Time frame: 16 week

    Functional problems related to the neck were assessed using the Neck Disability Index. The scale has 10 items. There are 6 options in each item and each option is scored between 0 and 5 depending on the severity of the limitation. Although the total score of the survey varies between 0 and 50, a higher score indicates an increase in limitation.

  3. Disability

    Time frame: 16 week

    Oswestry Disability Index was used to determine the degree of disability. The scale consists of a total of 10 items measuring the severity of pain, personal care, lifting, walking, sitting, standing, social life, sleeping, travel and pain degree. Each item is rated between 0-5. As the total score increases, the disability level increases. The maximum score is 50 points; Between 31 and 50 points is considered severe, between 11 and 30 points is considered moderate, and between 1 and 10 points is considered mild.

  4. Spine

    Time frame: 16 week

    Spine evaluation was performed with a spinal mouse device. The device is a computer-aided electromagnetic device that can be held by hand and used to measure spinal mobility in various postures.

Secondary outcomes

  1. Socio-demographic Form

    Time frame: 16 week

    Sociodemographic information of the caregivers, such as name, surname, age, gender, height, weight, BMI, and educational status, were recorded.

  2. Pain Intensity

    Time frame: 16 week

    The pain intensity of the patients was measured using the Visual Analogue Scale. The pain intensity score ranges from 0 to 10. An increase in the score indicates an increase in pain; a decrease in the score indicates a decrease in pain.

  3. Gross Motor Function Classification

    Time frame: 16 week

    Gross Motor Function Classification System (Children with Cerebral Palsy are classified in 5 levels (1-5) according to their motor skills, functional abilities, assistive technology and wheelchair requirements)

Sponsors and collaborators

Lead sponsor

Kirsehir Ahi Evran Universitesi

Other

Registry information

Official study title

Evaluation of the Spine of Primary Caregivers of Children with Cerebral Palsy

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jun 5, 2024
Registry last updated
Oct 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.