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Exercise Program for Individuals With SCI in Community

Study on the Safety and Effectiveness of a Rehabilitation Exercise Program for Individuals With Spinal Cord Injury in Community: A Randomized Controlled Trials

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06524453
Enrollment
58
Registered
2024-07-29
Start date
2024-08-01
Completion date
2025-08-31
Last updated
2025-05-29

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

Conditions

Exercise Program, Rehabilitation, Spinal Cord Injuries

Brief summary

Patients with spinal cord injury (SCI) who have reduced mobility have difficulty exercising on their own without proper guidance in the community. Community-based exercise programs are effective in removing various barriers such as lack of exercise programs, lack of experts, and lack of facilities. This study aims to verify the effectiveness and safety of a systematically designed customized exercise program for patients who live in the community and want to participate in exercise. Our study results will serve as a basis for creating an environment where more individuals with SCI can continue to exercise proactively and in the long term.

Detailed description

People with SCI must perform regular exercise to improve function, quality of life, and reduce medical costs. However, SCI people with reduced mobility have difficulty exercising on their own without proper guidance in the community. Rehabilitation exercise for SCI people should be applied based on accurate functional assessment, and risk factors related to exercise should also be assessed. Community-based exercise programs are effective in removing various barriers such as lack of exercise programs, lack of experts, and lack of facilities. This study aims to verify the effectiveness and safety of a systematically designed customized exercise program for SCI people who live in the community and want to participate in exercise. Based on the results of many previous studies, the investigators expect that program participants will have improved cardiopulmonary endurance and quality of life. Our study results will serve as a basis for creating an environment where more people with SCI can continue to exercise preemptively and in the long term.

Interventions

BEHAVIORALWheelchair accessible exercise program

1. Stretching exercise * Dynamic and static * Neck, shoulder, elbow, wrist, trunk * 10 minutes 2. Aerobic exercise * High intensity interval training * Arm ergometer or wheelchair running * 20 mins 3. Strengthening exercise * Shoulder and chest, elbow joint major muscle; shoulder and trunk stabilization exercise * 3 sets of 10 * 20 minutes 4. Stretching exercise * Dynamic and static * Neck, shoulder, elbow, wrist, trunk * 10 minutes

Sponsors

Pusan National University Yangsan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Spinal cord injury patients who are 19-65 years old or above and residing in the local community * Individuals who can not walk independently for more than 10 meters without assistance from others * Individuals whose elbow extensor strength is greater than muscle manual test (MMT) Fair

Exclusion criteria

* Individuals who have difficulty understanding the exercise program or expressing their symptoms * Individuals who cannot participate in the intervention exercise program due to serious cardiovascular diseases * Individuals who are deemed unsuitable for this study by a specialist in rehabilitation medicine due to other medical conditions

Design outcomes

Primary

MeasureTime frameDescription
6 minute push testBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programSub-maximal exercise test used to assess aerobic capacity and endurance. Longer distances indicate better athletic ability.

Secondary

MeasureTime frameDescription
Modified functional reach testBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programAssessing balance in sitting posture. Measures the maximum distance a person can extend forward while sitting in a fixed posture.
Grip strengthBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programForce applied by the hand to pull on or suspend from objects. It is widely used to assess sarcopenia and as a surrogate indicator of muscle strength. Measured in kg, the higher the value, the stronger the grip is considered.
Arm curlBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programTests upper limb endurance. Measures the number of times a participant can hold a dumbbell (4kg for men, 2kg for women) for 2 minutes and fully bend and straighten their arms. The higher the number, the better the function and strength.
Back scratch testBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programMeasures how close the hands can be brought together behind the back. If the fingertips touch then the score is zero. If they do not touch, measure the distance between the finger tips (a negative score), if they overlap, measure by how much (a positive score).
Beck anxiety inventoryBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programAnxiety measuring tool. Each item is scored 0-3 points, with a total score of 0-63 points. A score of 0-7 indicates minimal anxiety, a score of 8-15 indicates mild anxiety, a score of 16-25 indicates moderate anxiety, and a score of 26-63 indicates severe anxiety.
Spinal cord independence measure IIIBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programTool to evaluate independence of spinal cord injury patients. The total score ranges from 0 to 100, and the higher the score, the more independent the patient is.
Fat-free mass from bioelectrical impedance analysisBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programA method used to measure the components of the body. It is the total amount (kg) of body components excluding body fat, and the higher it is, the better the body composition is interpreted.
Fat-free mass index from bioelectrical impedance analysisBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programA method used to measure components of the body. This is an indicator that standardizes fat-free mass according to body size. The higher it is, the more muscle mass and the better health.
Percent body fat from bioelectrical impedance analysisBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programA method used to measure the components of the body. The normal range varies depending on age and gender. The lower the score within the general normal range, the better the health. The higher it is, the higher the risk of obesity related diseases.
skeletal muscle mass from bioelectrical impedance analysisBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programA method used to measure the components of the body. Normal range varies depending on age and gender. The higher it is within the general normal range, the better the health. The lower it is, the higher the risk of lack of strength and sarcopenia.
EuroQol 5 Dimension 5 LevelBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programSelf-report survey that measures quality of life across 5 domains: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Converting the patient's response results using quality weights has a value between 0.000 and 1.000. A higher score means a higher quality of life.
Beck depression inventoryBaseline evaluation and follow-up evaluation immediately after average 8-weeks of exercise programDepression measuring tool. Each item is scord 0-3 points, with a total score of 0-63 points. A score of 0-13 indicates minimal depression, a score of 14-19 indicates mild depression, a score of 20-28 indicates moderate depression, and a score of 29-63 indicates severe depression.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026