Elderly
Conditions
Keywords
Functional capacity, Quality of life, Depression, Falls, Body composition, Physical activity
Brief summary
The Health Enhancing Strength Training in Nonagenarians (STRONG) is a randomised control trial to assess the effectiveness of an aerobic and strength training program for improving functional capacity and quality of life in nonagenarians. Sixty (51 women) nonagenarians (age range: 90-102 years) who live in a geriatric nursing home will be randomly assigned to either a usual care (control) group (n=30) or an intervention (training) group (n=30). Participants allocated in the usual care group will receive general physical activity guidelines and participants allocated in the intervention group will also enroll in three weekly non-consecutive individualized training sessions (\ 45-50 min each) during 8 weeks. The exercise program will consist of muscular strength \[with a special focus on leg press at 30% (start of the program) to 70% 1 repetition maximum (end)\] and aerobic exercises (cycle-ergometry during 3-5 to 15 minutes at 12-14 points in the rate of perceived exertion scale). Results from STRONG will help to better understand the potential of regular physical activity for improving the well-being of the oldest population groups.
Interventions
Participants allocated in the intervention group will be enrolled in three weekly non-consecutive training sessions for 8 weeks. Each session will last for about 45-50 min. The exercise program will consist of muscular strength and aerobic exercises. Each session will start and end with a low intensity \ 5-7 min warm-up and cool-down period respectively, consisting mainly of stretching exercises involving all major muscle groups.
Sponsors
Study design
Eligibility
Inclusion criteria
* Age: 90 years or over. * Planning to stay in the same nursing home during the study. * Able to ambulate, with or without assistance. * Able to communicate. * Informed consent: Must be capable and willing to provide consent.
Exclusion criteria
* Acute or terminal illness. * Myocardial infarction in the past 3 months. * Not capable to ambulate. * Unstable cardiovascular disease or other medical condition. * Upper or lower extremity fracture in the past 3 months. * Severe dementia. * Unwillingness to either complete the study requirements or to be randomised into control or training group. * Presence of neuromuscular disease or drugs affecting neuromuscular function.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional capacity and quality of life | August 2009 |
Secondary
| Measure | Time frame |
|---|---|
| Depressive symptoms, falls and body composition | August 2009 |
Countries
Spain