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OpenTrials
Completed

NCT Number: NCT03201237

Comparison of Short- and Long-time Action Observation Training on Upper Limb Function in Children With Cerebral Palsy

To compared short- and long-time action observation training (AOT) in terms of grip strength, the Jebsen Taylor Hand Function Test (JTHF), the Quality of Upper Extremities Skills Test (QUEST), and the ABILHAND-Kids test.

Completed

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Key information

Age range

6 year–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Inje University

Gimhae, Gyeongsangnam-do, 621-749, South Korea

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ages between 6 and 15 years
  • confirmed diagnosis of spastic CP
  • below grade 2 on the modified Ashworth scale
  • between grade 4 and 8 on the house functional classification system
  • ability to understand the assessor's instructions.

Exclusion criteria

  • severe spasticity in UL (MAS>2)
  • orthopedic surgery in the UL within 6 months
  • absence of sensory

Treatment and study plan

Action Observation training

Other

Each child observed a task video and then performed a task

Primary outcomes

  1. Change of grip strength

    Time frame: 6 months

    Power of hand grip

Sponsors and collaborators

Lead sponsor

Inje University

Other

Registry information

Official study title

Main Researcher for Action Observation Training (AOT)

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Jun 28, 2017
Registry last updated
Jun 28, 2017

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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