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Promoting physical activity in individuals with spinal cord injury

Promoting physical activity in individuals with spinal cord injury - ACT-ACTIVE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34094
Enrollment
60
Registered
2010-06-29
Start date
2011-01-21
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

spinal cord injury spinal cord lesion

Interventions

The intervention will start 2 months before discharge from the rehabilitation center. Subjects will be randomized into two groups (FIT and Behave+FIT). Both groups receive an exercise intervention a

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Recent spinal cord injury - Between 18 and 65 years of age - Sufficient comprehension of the Dutch language to understand the purpose of the study and its testing methods - No progressive disease or a psychiatric condition that may interfere with participation

Exclusion criteria

Exclusion criteria: - Contraindications for exercise - Not able to perform the handcycle training intervention - Prognosis of becoming mainly ambulatory

Design outcomes

Primary

MeasureTime frame
The evaluation will primary contain objectively measured level of everyday physical activity (accelerometry-based activity monitor during 5 days). This measurement will be performed in both the FIT and Behave+FIT group at the beginning of the intervention period (T1), at discharge from the rehabilitation center (T2), 6 months after discharge (T3), and 1 year after discharge (T4).

Secondary

MeasureTime frame
Secondary parameters are: subjectively measured level of everyday physical activity (questionnaire), the effects on physical fitness (aerobic capacity), anthropometry (body mass index and waist circumference) and metabolic fitness (biochemical markers). Questionnaires will be used for functionality, fatigue, secondary problems, pain, social and sports participation, quality of life, self-efficacy, attitude, coping, and depression. Measurements will be performed in both groups at T1, T2, T3 and T4.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)