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The Development and Clinical Study of Exercise Program for Persons with Cervical Spinal Cord Injury

Development and Clinical Study of Rehabilitation Sports Program for Persons with Cervical Spinal Cord Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0005980
Enrollment
25
Registered
2021-03-09
Start date
2016-06-01
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

None listed

Interventions

Others(exercise intervention) : The program was developed in this study. Participants in the program participated in a total of 16 times, 60 minutes per session/twice a week/8 weeks.

Sponsors

National Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. A person with the highest level of cervical spinal cord injury (C3-C7) with complete motor nerve damage (ASIA A, B) 2. Currently non-smokers 3. Those who have never had chronic or acute heart disease or respiratory disease within the past or within 6 months 4. Those who had no comorbid damage such as deformation of the rib cage or fracture of the ribs prior to the occurrence of the accident. 5. Those who do not have spinal arthritis or neuromuscular disease that may affect lung function 6. A person who agrees to participate in the research, understands the words instructed by the researcher, and can fully cooperate in the research

Exclusion criteria

Exclusion criteria: 1. Persons with cervical spinal cord injury (C3-C7) who are not disabled 2. Current smokers 3. Those with chronic, acute heart disease and respiratory disease within the past or 6 months 4. A person who has suffered concomitant damage such as deformation of the rib cage or fracture of the ribs prior to the occurrence of the accident. 5. Those with spinal arthritis or neuromuscular disease that may affect lung function 6. Those who do not understand the words instructed by the researcher

Design outcomes

Primary

MeasureTime frame
Lung function test

Secondary

MeasureTime frame
muscle strength test;Quality of life;Depression;Satisfaction with the program and experience analysis

Countries

Korea, Republic of

Contacts

Public ContactDongheon Kang

National Rehabilitation Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 11, 2026