The purpose of this study is to develop a health promotion group intervention to meet the unique health promotion needs of people aging with SCI, to test the efficacy of the adapted intervention program, Living Longer and Stronger with SCI, in a randomized controlled trial and to assess the mechanisms through which the intervention may enhance physical, psychological, and social health.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Change in physical health as assessed by the SF-36 General Health Subscale
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in physical health as assessed by the Pain Intensity scale
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in physical health as assessed by the Interference scale
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in physical health as assessed by the SCI Secondary Conditions Scale (SCI-SCS)
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in psychological health and wellbeing as assessed by the Patient Health Questionaire-8 (PHQ-8)
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in psychological health and wellbeing as assessed by the Generalized Anxiety Disorder (GAD-2) scale
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in psychological health and wellbeing as assessed by the 4-itemPerceived Stress Scale (PSS)
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in psychological health and wellbeing as assessed by the SCI-Qol Positive Affect and Well-being Scale
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in psychological health and wellbeing as assessed by the Diener Satisfaction with Life Scale (SWLS)
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in social health as assessed by the UCLA Loneliness scale
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )
Change in social health as assessed by the Spinal Cord Injury - Quality of Life Scale (SCI-QOL) Satisfaction with Participation Scale
Timeframe: Baseline, end of intervention (8 weeks after baseline), follow up (4 months after end of intervention )