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OpenTrials
Completed

NCT Number: NCT07347483

Assessment of Trunk Position Sense, Trunk Control, and Functional Independence in Children With Cerebral Palsy

The purpose of this study is to determine whether there is a difference in trunk proprioception, as assessed by trunk position sense, in children with unilateral and bilateral spastic cerebral palsy, and to evaluate the relationship between trunk position sense, trunk control, and functional independence.

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Key information

Age range

6 year–12 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Sivas Cumhuriyet University

Sivas, 58140, Turkey (Türkiye)

About this study

This cross-sectional and descriptive study was conducted in children with unilateral and bilateral spastic cerebral palsy aged between 6 and 12 years. A total of 78 children (36 girls and 42 boys) with spastic cerebral palsy were included in the study. The gross motor function levels of the participants ranged from Level I to Level IV according to the Gross Motor Function Classification System (GMFCS).

Participants were recruited from children receiving education and rehabilitation services at special education and rehabilitation centers in Kayseri, Turkiye, and only children whose parents or legal guardians provided written informed consent were included.

Demographic and clinical characteristics of the participants were recorded using a structured sociodemographic data form.

Trunk position sense was assessed using a dual inclinometer device to evaluate trunk proprioception. Trunk control was evaluated using the Trunk Impairment Scale, and functional independence was assessed using the motor subscale of the Pediatric Functional Independence Measure (WeeFIM). In addition, muscle tone was assessed bilaterally using the Modified Ashworth Scale.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Have a diagnosis of unilateral or bilateral spastic cerebral palsy,
  • Are aged between 6 and 12 years,
  • Are able to sit independently,
  • Have a cognitive level sufficient to understand and follow verbal instructions,
  • Have not undergone surgical intervention or Botulinum Toxin A injection within the last 6 months,
  • Have parents or legal guardians who have provided written informed consent.

Exclusion criteria

  • Have received Botulinum Toxin or intrathecal baclofen treatment within the last 6 months,
  • Have a history of pelvic, spinal, or upper extremity surgery,
  • Have severe visual or hearing impairments,
  • Have cognitive impairments preventing effective communication,
  • Are unable to sit independently,
  • Do not have parental consent.

Treatment and study plan

Only measurements were taken.

Other

This study does not contain any intervention.

Primary outcomes

  1. Trunk Position Sense

    Time frame: Data collection was conducted between January 2022 and March 2023.

    Trunk proprioception assessed using a dual inclinometer device during trunk flexion movements with the repositioning angle method under eyes-open and eyes-closed conditions.

Secondary outcomes

  1. Trunk Control

    Time frame: January 2022 - March 2023

    Assessed using the Trunk Impairment Scale (TIS) in sitting position.

  2. Functional Independence

    Time frame: January 2022 - March 2023

    Assessed using the motor subscale of the Pediatric Functional Independence Measure (WeeFIM).

  3. Muscle Tone

    Time frame: January 2022 - March 2023

    Assessed bilaterally using the Modified Ashworth Scale (MAS).

Sponsors and collaborators

Lead sponsor

Cumhuriyet University

Other

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jan 16, 2026
Registry last updated
Jan 16, 2026

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.

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