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Effect of an exercise program on neuropathic and musculoskeletal pain intensity in spinal cord injury patients

Effect of an exercise program on neuropathic and musculoskeletal pain intensity in spinal cord injury patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015051822311N1
Enrollment
40
Registered
2015-08-01
Start date
2014-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Spinal cord injury. Injury to nerves and spinal cord

Interventions

Intervention 1: Intervention group 1: The intervention consisted of 12 sessions of 45 to 60 minutes exercise program for patients with spinal cord injuries paraplegia caused by Canadian spinal cord in
Treatment - Other
Intervention group 1: The intervention consisted of 12 sessions of 45 to 60 minutes exercise program for patients with spinal cord injuries paraplegia caused by Canadian spinal cord injuries center an
Control group: No intervention

Sponsors

Vice chancellor for research, University of Social Welfare and Rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria:Consent to participate in research and cooperation necessar;Patients not participate in exercise programs Last three months; history of spinal cord injury for 6 months and more; not having chronic disease as high blood pressure and epilepsy and...; not having Vertebral disc prolapse; not Having a history of severe trauma; Non- alcohol drug addiction; The level of spinal cord injury should be thoracic , lumbar or sacral that named paraplegia;Not pregnant (for women); All participants should be use of a same manual wheelchair to suit their own physical condition; Earn score of 4 or higher on a scale measuring pain intensity score;Ability to read manual by themselves or relatives and the ability to perform intervention. Exclusion criteria:Cancel the continued cooperation; The absence of more than 3 times the intervention meetings; intensifying of symptoms and spinal disorders; Defects of the nervous and cardiovascular disorders during the intervention

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Neuropathic pain intensity. Timepoint: Before and 2 months after the intervention. Method of measurement: International Spinal Cord Injury Basic Pain Data Set.;Musculoskeletal pain intensity. Timepoint: Before and 2 months after the intervention. Method of measurement: International Spinal Cord Injury Basic Pain Data Set.

Secondary

MeasureTime frame
---. Timepoint: ---. Method of measurement: ---.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaser Sedghi Goyaghaj

University of Social Welfare and Rehabilitation sciences

sedghi.nurse@yahoo.com+98 21 3640 0459

Outcome results

None listed

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