跳至主要内容
临床试验/NCT03627793
NCT03627793Unknown不适用

Resistance Exercise Training at Different Intensities in Healthy and Frail Older People: A Feasibility Study

University of Glasgow1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2018年8月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
60
试验地点
1
主要终点
Number of training sessions attended

研究概览

简要总结

After the age of 40-45 years muscle mass and function progressively decline, reducing older peoples' abilities to perform tasks of daily living and also increase the risk of falls. It is known that, across the life course, resistance exercise can be of benefit in increasing muscle mass and function, yet how hard the exercise should be performed has received little attention. Current recommendations are for older people to perform exercise at 70% of the maximum they can lift, quite a high intensity that often puts older people off participating. Recent evidence in younger people has suggested that such intensities are not required.

The investigators aim to determine the feasibility of a study to investigate recruitment and adherence of older people to a study of exercise training at different intensities.

详细描述

The cohort will comprise two sets of participants: frail older adults and non-frail older adults.

Each participant will receive 8 weeks of twice weekly supervised resistance training. Both the frail and non-frail participants will be randomised into either receiving high load resistance training or low load resistance training. High load resistance training will be delivered at 70% of the participants maximal capacity and low load resistance training will be delivered at 30% of maximal capacity. All resistance training will focus on the lower limb and regardless of intensity each exercise will be done to failure (unable to complete another full repetition).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Non-frail - Over 65 years of age Frail - Over 65 years of age, Three or more of the following criteria: >10lbs of weight loss unintentionally in previous year; grip strength in lowest 20% (by sex and BMI); self-reported exhaustion; walking time for 15 feet in slowest 20% (by sex and height); physical activity in the lowest 20%.

排除标准

  • Non-frail - Current participation in an exercise programme. Clinical team do not think resistance exercise would be safe or unable to consent. Any other reason that precludes participation in exercise, decision made by research team in consultation with a consultant in Geriatric Medicine where required.
  • Frail - Current participation in an exercise programme. Clinical team do not think resistance exercise would be safe or unable to consent. Any other reason that precludes participation in exercise, decision made by research team in consultation with a consultant in Geriatric Medicine where required.

研究组 & 干预措施

High load non-frail

Active Comparator

Non-frail participants who will receive resistance training at 70% of their maximal strength

干预措施: resistance training (Other)

low load non-frail

Active Comparator

Non-frail participants who will receive resistance training at 30% of their maximal strength

干预措施: resistance training (Other)

high load frail

Experimental

Frail participants who will receive resistance training at 70% of their maximal strength

干预措施: resistance training (Other)

low load frail

Experimental

Frail participants who will receive resistance training at 30% of their maximal strength

干预措施: resistance training (Other)

结局指标

主要结局

Number of training sessions attended

时间窗: 8 weeks

Expressed as a percentage of number of sessions attended

Compliance with protocol

时间窗: 8 weeks

Expressed as a percentage of number of sessions where training protocol was adhered to

Number of treatment-related adverse events as assessed by CTCAE v4.0

时间窗: 8 weeks

Number of adverse events that could be attributed to the intervention

Acceptability of intervention (qualitative)

时间窗: 8 weeks

focus groups with semi-structured discussion plans will investigate the acceptability of the intervention

次要结局

  • Muscle strength(8 weeks)
  • Muscle power(8 weeks)
  • Muscle thickness(8 weeks)
  • Frailty(8 weeks)
  • Quality of life(8 weeks)
  • Functional abilities(8 weeks)
  • motion analysis(8 weeks)
  • Activities of daily living(8 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Evan Campbell

Research Associate

University of Glasgow

研究点 (1)

Loading locations...

相似试验