Health Enhancing Strength Training in Nonagenarians
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Functional capacity and quality of life
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Single (Investigator)
入排标准
- 年龄范围
- 90 Years 至 110 Years(Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •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.
排除标准
- •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.
研究组 & 干预措施
2
The experimental group will participate in the aerobic and strength training program.
干预措施: 8-week aerobic and strength training program (Behavioral)
1
The usual care group will receive general physical activity guidelines.
结局指标
主要结局
Functional capacity and quality of life
时间窗: August 2009
次要结局
- Depressive symptoms, falls and body composition(August 2009)
研究者
Jose Antonio Serra
MD PhD Head of Department(Geriatry)
Hospital General Universitario Gregorio Marañon
