Skip to content

ambulation of SCI paraplegic patients with LEX mark 3

evaluation of rehabilitation and gait of SCI paraplegic patients using LEX mark 3 device

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190225042840N1
Enrollment
8
Registered
2019-10-18
Start date
2019-09-11
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Condition 1: paraplegic patients with thoracic spinal cord injury. Condition 2: lumbar spinal cord injury. Concussion and edema of thoracic spinal cord, sequela Concussion and edema of lumbar spinal cord, sequela

Interventions

Intervention group: Paraplegic patients using a functional electrical stimulation device for rehabilitation.

Sponsors

Brain Mapping Center of Loghman Hakim Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: paraplegic patients with loss of sense in lower extremities. paraplegic patients with loss of voluntary movements. normal function of upper extremities.

Exclusion criteria

Exclusion criteria: autonomic dysreflexia presence of malignancy in lower extremities at electrode junctions presence of ulcer in lower extremities at electrode junctions any kind of deformity in lower extremities,trunk or upper extremities

Design outcomes

Primary

MeasureTime frame
The third variable of the study is the number of sessions needed to train patients to use the device. Timepoint: In this study, the number of sessions required for patients after completing their training is evaluated and calculated. The total number of sessions will be calculated when patients have the necessary ability to use the device to get up and walk. Method of measurement: The number of patient training sessions will be recorded in the office and the number of sessions will be calculated based on the days recorded.;The ambulation pace of patients is the result of the distance traveled by the duration of walking in each session. Timepoint: At the end of each training session, the distance traveled by the patients is recorded and divided to the duration of travel. Method of measurement: This variable is obtained by dividing the distance traveled by time. The unit of measurement is meters per second.;The first variable is the distance traveled by the patient using the device.Its definition includes the displacement performed by patients by lower extremities and with the aid of the device. Timepoint: The time to measure this variable is at the end of each training session. Method of measurement: The distance traveled by patients will be measured and recorded.;The second variable in this study is the duration of walking and standing of each patient. Its definition includes amount of time spent by the patient walking and standing during a session. Timepoint: The time to measure this variable is at the end of each training sessions. Method of measurement: Minutes are route of measurement and reporting this variable.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSam Alahyari

Shahid Beheshti University of Medical Sciences

allahyarisam@yahoo.com+98 21 2293 8669

Outcome results

None listed

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