Comparative study on the therapeutic effects of two lower limb rehabilitation robots, Relink muscle armor and Lokomat, on improving lower limb motor function in children with cerebral palsy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300073972

Enrollment

Unknown

Registered

2023-07-26

Start date

2023-08-01

Completion date

Unknown

Last updated

2023-07-30

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

Conditions

cerebral palsy

Interventions

2:Kinesiotherapy+paraffin therapy+neuromuscular electric stimulation therapy+massage therapy+Relink muscle nail lower limb Exoskeleton robot training

1:Exercise therapy+paraffin therapy+neuromuscular electric stimulation therapy+massage therapy+Lokomat lower limb Exoskeleton robot training

Eligibility

Sex/Gender

All

Age

3 Years to 10 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria (all of the following conditions must be met): ? Conforming to the diagnostic and classification criteria for cerebral palsy, with a GMFCS rating of II - III, and a modified Ashworth spasticity grading scale rating of I - III. ? Age 3-10 years old, able to understand instructions and cooperate in completing training. ? Able to walk for 6 minutes with or without auxiliary equipment. ? Those who have not undergone surgical correction surgery or botulinum toxin injection treatment in the past 6 months. ? The family members have informed consent and voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria (meeting any of the following conditions): ? Complications with important organs such as heart, liver, and kidney. ? It is accompanied by severe epilepsy, genetic metabolic disease and severe Skeleton disease. ? Concomitant severe coagulation dysfunction and thrombotic disease. ? Concomitant severe unhealed skin lesions of the lower limbs. ? Combined with acute or progressive Nervous system disease. ? The researchers believe that there are other factors that are not suitable for children to participate in this study.

Design outcomes

Primary

Measure	Time frame
10-meter walking test;6-minute walking test;Gross motor function test score;Child balance scale score;Modified Tardieu Scale;Edinburgh Visual Gait Score;Physiological consumption index;	—

Countries

China

Contacts

Public ContactZhu Dengna

The Third Affiliated Hospital of Zhengzhou University

zhudengna@126.com+86 138 3814 1626

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026