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Effects of body weight supported treadmill training along with electrical stimulation on functional ambulation, pain and quality of life in patients with incomplete traumatic-spinal cord injury.

Effects of Body Weight Supported Treadmill Training along with Electrical Stimulation on Functional Ambulation, Pain and Quality Of Life in Patients with Incomplete Traumatic Spinal Cord Injury

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230615058487N1
Enrollment
81
Registered
2023-07-29
Start date
2023-05-13
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Spinal cord injury. Injury of spinal cord, level unspecified

Interventions

Intervention 1: Intervention group 1: This Intervention group will receive BWSTT along with electrical stimulation (ES) and conventional physical therapy. Intervention 2: Intervention group 2:This Int

Sponsors

Paraplegic Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 55 Years

Inclusion criteria

Inclusion criteria: Patients aged between 16-55 years Both male and female patients Patients with incomplete traumatic SCIs (ASIA scale B, C, D) Patients with stable spines Patients in the sub-acute rehabilitation phase Patients with mild neuropathic pain (1-3 on VAS)

Exclusion criteria

Exclusion criteria: Patients in acute phase of rehabilitation Patients with pressure sores, infections or other complications Patients with visual impairments that may impact participation in rehabilitation

Design outcomes

Primary

MeasureTime frame
Functional ambulation. Timepoint: Before intervention and , 6 ,12 week after intervention. Method of measurement: Walking Index for Spinal Cord Injuries-II,Spinal Cord Independence Measure (SCIM),6-Minute Walk Test (6MWT) and 10-Meter Walk Test.

Secondary

MeasureTime frame
Neuropathic pain level and inflammatory pain markers, and Quality Life Index for spinal cord injury. Timepoint: Before intervention and 6,12 weeks after intervention. Method of measurement: Visual Analog Scale (VAS), Neuropathic Pain Diagnostic Questionnaire along with blood tests and Quality Life Index for spinal cord injury.

Countries

Pakistan

Contacts

Public ContactDr. Amir Zeb

Riphah College of Rehabilitation & Allied Health Sciences

amir_zeb45@yahoo.com+92 42 111 747 424

Outcome results

None listed

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