The effects of body weight supported overground walking training on gait kinematic and kinetics in chronic hemiplegic patients: single center, single blind, randomized controlled parallel study

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002046

Enrollment

Registered

2016-09-09

Start date

2016-04-14

Completion date

Unknown

Last updated

2021-05-24

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

Conditions

None listed

Interventions

Medical Device : Ground-based walking group receives walking training on the ground as the rehabilitation protocol, whereas partial body weight support group receives a rehabilitation training that ut

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: inclusion criteria - Adults (19 years and older) - Post-stroke patients (At least 6 months after the initial stroke) - Patients who are able to walk 10m independently without a walking assistance device - Patients who voluntarily participated in the clinical trial

Exclusion criteria

Exclusion criteria: exclusion criteria - Patients who showed a full recovery after a stroke ? Exclusion of patients at a full recovery state with a score of 0-1 according to the modified Rankin Scale (mRS) - Patients with internal or musculoskeletal complications (Arthrogryposis, severe pain, etc.) that restrict participation in exercises - Patients with bilateral hemiplegia due to either multiple stroke syndrome or recurrent strokes - Patients with weight over 120kg - Patients with visual impairment - Patients with lower limb fracture experiences within the recent 2 months - Patients with hip instability or history of hip dislocation - Patients with ischial decubitus ulcers or lower limb ulcers - Patients with lower limb amputations - Patients with severe acute diseases (internal/external) - Patients with neurodegenerative diseases that result in walking impairment, such as Parkinson’s disease - Patients with severe depression - Patients with severe aphasia or cognitive impairment who meet level-2 criteria (difficulty in following verbal instructions) - Patients with implantable electronic medical devices, such as a pacemaker - Patients who use electrical life support equipment, such as a cardiopulmonary bypass (CPB) machine - Patients who use wearable medical devices, such as a cardiac monitor - High fever patients - Pregnant patients (including lactating women and those with pregnancy plans)

Design outcomes

Primary

Measure	Time frame
3D-gait analysis	—

Secondary

Measure	Time frame
10-meter walking test;Timed up and go test (TUG);TecnoBody;FAC (Functional Ambulatory Category)	—

Countries

Korea, Republic of

Contacts

Public ContactKim Yop

Chonnam National University Hospital

office4@naver.com+82-62-220-5186

Outcome results